---
_id: '4425'
abstract:
- lang: eng
  text: "Giotto provides a time-triggered programmer’s model for the implementation
    of embedded control systems with hard real-time constraints. Giotto’s precise
    semantics and predictabil- ity make it suitable for safety-critical applications.\r\nGiotto
    is based around the idea that time-triggered task invocation together with time-triggered
    mode switching can form a useful programming model for real-time systems. To substantiate
    this claim, we describe the use of Giotto to refactor the software of a small,
    autonomous helicopter. The ease with which Giotto expresses the existing software
    provides evidence that Giotto is an appropriate programming language for control
    systems.\r\nSince Giotto is a real-time programming language, ensuring that Giotto
    programs meet their deadlines is crucial. To study precedence-constrained Giotto
    scheduling, we first examine single-mode, single-processor scheduling. We extend
    to an infinite, periodic setting the classical problem of meeting deadlines for
    a set of tasks with release times, deadlines, precedence constraints, and preemption.
    We then develop an algorithm for scheduling Giotto programs on a single processor
    by representing Giotto programs as instances of the extended scheduling problem.\r\nNext,
    we study multi-mode, single-processor Giotto scheduling. This problem is different
    from classical scheduling problems, since in our precedence-constrained approach,
    the deadlines of tasks may vary depending on the mode switching behavior of the
    program. We present conditional scheduling models which capture this varying-deadline
    behavior. We develop polynomial-time algorithms for some conditional scheduling
    models, and prove oth- ers to be computationally hard. We show how to represent
    multi-mode Giotto programs as instances of the model, resulting in an algorithm
    for scheduling multi-mode Giotto programs on a single processor.\r\nFinally, we
    show that the problem of scheduling Giotto programs for multiple net- worked processors
    is strongly NP-hard."
article_processing_charge: No
author:
- first_name: Benjamin
  full_name: Horowitz, Benjamin
  last_name: Horowitz
citation:
  ama: 'Horowitz B. Giotto: A time-triggered language for embedded programming. 2003:1-237.'
  apa: 'Horowitz, B. (2003). <i>Giotto: A time-triggered language for embedded programming</i>.
    University of California, Berkeley.'
  chicago: 'Horowitz, Benjamin. “Giotto: A Time-Triggered Language for Embedded Programming.”
    University of California, Berkeley, 2003.'
  ieee: 'B. Horowitz, “Giotto: A time-triggered language for embedded programming,”
    University of California, Berkeley, 2003.'
  ista: 'Horowitz B. 2003. Giotto: A time-triggered language for embedded programming.
    University of California, Berkeley.'
  mla: 'Horowitz, Benjamin. <i>Giotto: A Time-Triggered Language for Embedded Programming</i>.
    University of California, Berkeley, 2003, pp. 1–237.'
  short: 'B. Horowitz, Giotto: A Time-Triggered Language for Embedded Programming,
    University of California, Berkeley, 2003.'
date_created: 2018-12-11T12:08:47Z
date_published: 2003-10-01T00:00:00Z
date_updated: 2021-01-12T07:56:53Z
day: '01'
extern: '1'
language:
- iso: eng
month: '10'
oa_version: None
page: 1 - 237
publication_status: published
publisher: University of California, Berkeley
publist_id: '305'
status: public
supervisor:
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000-0002-2985-7724
title: 'Giotto: A time-triggered language for embedded programming'
type: dissertation
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2003'
...
---
_id: '4460'
abstract:
- lang: eng
  text: "Symbolic model checking, which enables the automatic verification of large
    systems, proceeds by calculating expressions that represent state sets. Traditionally,
    symbolic model-checking tools are based on back- ward state traversal; their basic
    operation is the function pre, which, given a set of states, returns the set of
    all predecessor states. This is because specifiers usually employ formalisms with
    future-time modalities, which are naturally evaluated by iterating applications
    of pre. It has been shown experimentally that symbolic model checking can perform
    significantly better if it is based, instead, on forward state traversal; in this
    case, the basic operation is the function post, which, given a set of states,
    returns the set of all successor states. This is because forward state traversal
    can ensure that only parts of the state space that are reachable from an initial
    state and relevant for the satisfaction or violation of the specification are
    explored; that is, errors can be detected as soon as possible.\r\nIn this paper,
    we investigate which specifications can be checked by symbolic forward state traversal.
    We formulate the problems of symbolic backward and forward model checking by means
    of two μ-calculi. The pre-μ calculus is based on the pre operation, and the post-μ
    calculus is based on the post operation. These two μ-calculi induce query logics,
    which augment fixpoint expressions with a boolean emptiness query. Using query
    logics, we are able to relate and compare the symbolic backward and forward approaches.
    In particular, we prove that all ω-regular (linear-time) specifications can be
    expressed as post-μ queries, and therefore checked using symbolic forward state
    traversal. On the other hand, we show that there are simple branching-time specifications
    that cannot be checked in this way."
acknowledgement: This research was supported in part by the SRC contract 99-TJ-683.003
  and the NSF grant CCR-9988172.
article_processing_charge: No
article_type: original
author:
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000−0002−2985−7724
- first_name: Orna
  full_name: Kupferman, Orna
  last_name: Kupferman
- first_name: Shaz
  full_name: Qadeer, Shaz
  last_name: Qadeer
citation:
  ama: Henzinger TA, Kupferman O, Qadeer S. From pre-historic to post-modern symbolic
    model checking. <i>Formal Methods in System Design</i>. 2003;23(3):303-327. doi:<a
    href="https://doi.org/10.1023/A:1026228213080">10.1023/A:1026228213080</a>
  apa: Henzinger, T. A., Kupferman, O., &#38; Qadeer, S. (2003). From pre-historic
    to post-modern symbolic model checking. <i>Formal Methods in System Design</i>.
    Springer. <a href="https://doi.org/10.1023/A:1026228213080">https://doi.org/10.1023/A:1026228213080</a>
  chicago: Henzinger, Thomas A, Orna Kupferman, and Shaz Qadeer. “From Pre-Historic
    to Post-Modern Symbolic Model Checking.” <i>Formal Methods in System Design</i>.
    Springer, 2003. <a href="https://doi.org/10.1023/A:1026228213080">https://doi.org/10.1023/A:1026228213080</a>.
  ieee: T. A. Henzinger, O. Kupferman, and S. Qadeer, “From pre-historic to post-modern
    symbolic model checking,” <i>Formal Methods in System Design</i>, vol. 23, no.
    3. Springer, pp. 303–327, 2003.
  ista: Henzinger TA, Kupferman O, Qadeer S. 2003. From pre-historic to post-modern
    symbolic model checking. Formal Methods in System Design. 23(3), 303–327.
  mla: Henzinger, Thomas A., et al. “From Pre-Historic to Post-Modern Symbolic Model
    Checking.” <i>Formal Methods in System Design</i>, vol. 23, no. 3, Springer, 2003,
    pp. 303–27, doi:<a href="https://doi.org/10.1023/A:1026228213080">10.1023/A:1026228213080</a>.
  short: T.A. Henzinger, O. Kupferman, S. Qadeer, Formal Methods in System Design
    23 (2003) 303–327.
date_created: 2018-12-11T12:08:58Z
date_published: 2003-06-20T00:00:00Z
date_updated: 2024-01-10T11:50:31Z
day: '20'
doi: 10.1023/A:1026228213080
extern: '1'
intvolume: '        23'
issue: '3'
language:
- iso: eng
month: '06'
oa_version: None
page: 303 - 327
publication: Formal Methods in System Design
publication_identifier:
  issn:
  - 0925-9856
publication_status: published
publisher: Springer
publist_id: '268'
quality_controlled: '1'
scopus_import: '1'
status: public
title: From pre-historic to post-modern symbolic model checking
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 23
year: '2003'
...
---
_id: '4462'
abstract:
- lang: eng
  text: 'A major hurdle in the algorithmic verification and control of systems is
    the need to find suitable abstract models, which omit enough details to overcome
    the state-explosion problem, but retain enough details to exhibit satisfaction
    or controllability with respect to the specification. The paradigm of counterexample-guided
    abstraction refinement suggests a fully automatic way of finding suitable abstract
    models: one starts with a coarse abstraction, attempts to verify or control the
    abstract model, and if this attempt fails and the abstract counterexample does
    not correspond to a concrete counterexample, then one uses the spurious counterexample
    to guide the refinement of the abstract model. We present a counterexample-guided
    refinement algorithm for solving ω-regular control objectives. The main difficulty
    is that in control, unlike in verification, counterexamples are strategies in
    a game between system and controller. In the case that the controller has no choices,
    our scheme subsumes known counterexample-guided refinement algorithms for the
    verification of ω-regular specifications. Our algorithm is useful in all situations
    where ω-regular games need to be solved, such as supervisory control, sequential
    and program synthesis, and modular verification. The algorithm is fully symbolic,
    and therefore applicable also to infinite-state systems.'
acknowledgement: This research was supported in part by the DARPA SEC grant F33615-C-98-3614,
  the ONR grant N00014-02-1-0671, and the NSF grants CCR-9988172, CCR-0085949, and
  CCR-0225610.
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000−0002−2985−7724
- first_name: Ranjit
  full_name: Jhala, Ranjit
  last_name: Jhala
- first_name: Ritankar
  full_name: Majumdar, Ritankar
  last_name: Majumdar
citation:
  ama: 'Henzinger TA, Jhala R, Majumdar R. Counterexample-guided control. In: <i>Proceedings
    of the 30th International Colloquium on Automata, Languages and Programming</i>.
    Vol 2719. Springer; 2003:886-902. doi:<a href="https://doi.org/10.1007/3-540-45061-0_69">10.1007/3-540-45061-0_69</a>'
  apa: 'Henzinger, T. A., Jhala, R., &#38; Majumdar, R. (2003). Counterexample-guided
    control. In <i>Proceedings of the 30th International Colloquium on Automata, Languages
    and Programming</i> (Vol. 2719, pp. 886–902). Eindhoven, The Netherlands: Springer.
    <a href="https://doi.org/10.1007/3-540-45061-0_69">https://doi.org/10.1007/3-540-45061-0_69</a>'
  chicago: Henzinger, Thomas A, Ranjit Jhala, and Ritankar Majumdar. “Counterexample-Guided
    Control.” In <i>Proceedings of the 30th International Colloquium on Automata,
    Languages and Programming</i>, 2719:886–902. Springer, 2003. <a href="https://doi.org/10.1007/3-540-45061-0_69">https://doi.org/10.1007/3-540-45061-0_69</a>.
  ieee: T. A. Henzinger, R. Jhala, and R. Majumdar, “Counterexample-guided control,”
    in <i>Proceedings of the 30th International Colloquium on Automata, Languages
    and Programming</i>, Eindhoven, The Netherlands, 2003, vol. 2719, pp. 886–902.
  ista: 'Henzinger TA, Jhala R, Majumdar R. 2003. Counterexample-guided control. Proceedings
    of the 30th International Colloquium on Automata, Languages and Programming. ICALP:
    Automata, Languages and Programming, LNCS, vol. 2719, 886–902.'
  mla: Henzinger, Thomas A., et al. “Counterexample-Guided Control.” <i>Proceedings
    of the 30th International Colloquium on Automata, Languages and Programming</i>,
    vol. 2719, Springer, 2003, pp. 886–902, doi:<a href="https://doi.org/10.1007/3-540-45061-0_69">10.1007/3-540-45061-0_69</a>.
  short: T.A. Henzinger, R. Jhala, R. Majumdar, in:, Proceedings of the 30th International
    Colloquium on Automata, Languages and Programming, Springer, 2003, pp. 886–902.
conference:
  end_date: 2003-07-04
  location: Eindhoven, The Netherlands
  name: 'ICALP: Automata, Languages and Programming'
  start_date: 2003-06-30
date_created: 2018-12-11T12:08:58Z
date_published: 2003-06-25T00:00:00Z
date_updated: 2024-01-10T11:19:41Z
day: '25'
doi: 10.1007/3-540-45061-0_69
extern: '1'
intvolume: '      2719'
language:
- iso: eng
month: '06'
oa_version: None
page: 886 - 902
publication: Proceedings of the 30th International Colloquium on Automata, Languages
  and Programming
publication_identifier:
  isbn:
  - '9783540404934'
publication_status: published
publisher: Springer
publist_id: '265'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Counterexample-guided control
type: conference
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 2719
year: '2003'
...
---
_id: '4463'
abstract:
- lang: eng
  text: We present an algorithm called TAR (“Thread-modular Abstraction Refinement”)
    for model checking safety properties of concurrent software. The TAR algorithm
    uses thread-modular assume-guarantee reasoning to overcome the exponential complexity
    in the control state of multithreaded programs. Thread modularity means that TAR
    explores the state space of one thread at a time, making assumptions about how
    the environment can interfere. The TAR algorithm uses counterexample-guided predicate-abstraction
    refinement to overcome the usually infinite complexity in the data state of C
    programs. A successive approximation scheme automatically infers the necessary
    precision on data variables as well as suitable environment assumptions. The scheme
    is novel in that transition relations are approximated from above, while at the
    same time environment assumptions are approximated from below. In our software
    verification tool BLAST we have implemented a fully automatic race checker for
    multithreaded C programs which is based on the TAR algorithm. This tool has verified
    a wide variety of commonly used locking idioms, including locking schemes that
    are not amenable to existing dynamic and static race checkers such as ERASER or
    WARLOCK.
acknowledgement: This work was supported in part by the NSF grants CCR-0085949 and
  CCR-0234690, the DARPA grant F33615-00-C-1693, and the MARCO grant 98-DT-660.
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000−0002−2985−7724
- first_name: Ranjit
  full_name: Jhala, Ranjit
  last_name: Jhala
- first_name: Ritankar
  full_name: Majumdar, Ritankar
  last_name: Majumdar
- first_name: Shaz
  full_name: Qadeer, Shaz
  last_name: Qadeer
citation:
  ama: 'Henzinger TA, Jhala R, Majumdar R, Qadeer S. Thread-modular abstraction refinement.
    In: <i>Proceedings of the 15th International Conference on Computer Aided Verification</i>.
    Vol 2725. Springer; 2003:262-274. doi:<a href="https://doi.org/10.1007/978-3-540-45069-6_27">10.1007/978-3-540-45069-6_27</a>'
  apa: 'Henzinger, T. A., Jhala, R., Majumdar, R., &#38; Qadeer, S. (2003). Thread-modular
    abstraction refinement. In <i>Proceedings of the 15th International Conference
    on Computer Aided Verification</i> (Vol. 2725, pp. 262–274). Boulder, CO, USA:
    Springer. <a href="https://doi.org/10.1007/978-3-540-45069-6_27">https://doi.org/10.1007/978-3-540-45069-6_27</a>'
  chicago: Henzinger, Thomas A, Ranjit Jhala, Ritankar Majumdar, and Shaz Qadeer.
    “Thread-Modular Abstraction Refinement.” In <i>Proceedings of the 15th International
    Conference on Computer Aided Verification</i>, 2725:262–74. Springer, 2003. <a
    href="https://doi.org/10.1007/978-3-540-45069-6_27">https://doi.org/10.1007/978-3-540-45069-6_27</a>.
  ieee: T. A. Henzinger, R. Jhala, R. Majumdar, and S. Qadeer, “Thread-modular abstraction
    refinement,” in <i>Proceedings of the 15th International Conference on Computer
    Aided Verification</i>, Boulder, CO, USA, 2003, vol. 2725, pp. 262–274.
  ista: 'Henzinger TA, Jhala R, Majumdar R, Qadeer S. 2003. Thread-modular abstraction
    refinement. Proceedings of the 15th International Conference on Computer Aided
    Verification. CAV: Computer Aided Verification, LNCS, vol. 2725, 262–274.'
  mla: Henzinger, Thomas A., et al. “Thread-Modular Abstraction Refinement.” <i>Proceedings
    of the 15th International Conference on Computer Aided Verification</i>, vol.
    2725, Springer, 2003, pp. 262–74, doi:<a href="https://doi.org/10.1007/978-3-540-45069-6_27">10.1007/978-3-540-45069-6_27</a>.
  short: T.A. Henzinger, R. Jhala, R. Majumdar, S. Qadeer, in:, Proceedings of the
    15th International Conference on Computer Aided Verification, Springer, 2003,
    pp. 262–274.
conference:
  end_date: 2003-07-12
  location: Boulder, CO, USA
  name: 'CAV: Computer Aided Verification'
  start_date: 2003-07-08
date_created: 2018-12-11T12:08:59Z
date_published: 2003-06-27T00:00:00Z
date_updated: 2024-01-10T11:05:53Z
day: '27'
doi: 10.1007/978-3-540-45069-6_27
extern: '1'
intvolume: '      2725'
language:
- iso: eng
month: '06'
oa_version: None
page: 262 - 274
publication: Proceedings of the 15th International Conference on Computer Aided Verification
publication_identifier:
  isbn:
  - '9783540405245'
publication_status: published
publisher: Springer
publist_id: '266'
quality_controlled: '1'
status: public
title: Thread-modular abstraction refinement
type: conference
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 2725
year: '2003'
...
---
_id: '4464'
abstract:
- lang: eng
  text: We introduce the paradigm of schedule-carrying code (SCC). A hard real-time
    program can be executed on a given platform only if there exists a feasible schedule
    for the real-time tasks of the program. Traditionally, a scheduler determines
    the existence of a feasible schedule according to some scheduling strategy. With
    SCC, a compiler proves the existence of a feasible schedule by generating executable
    code that is attached to the program and represents its schedule. An SCC executable
    is a real-time program that carries its schedule as code, which is produced once
    and can be revalidated and executed with each use. We evaluate SCC both in theory
    and practice. In theory, we give two scenarios, of nonpreemptive and distributed
    scheduling for Giotto programs, where the generation of a feasible schedule is
    hard, while the validation of scheduling instructions that are attached to the
    programs is easy. In practice, we implement SCC and show that explicit scheduling
    instructions can reduce the scheduling overhead up to 35% and can provide an efficient,
    flexible, and verifiable means for compiling Giotto programs on complex architectures,
    such as the TTA.
acknowledgement: This work was supported by the AFOSR MURI grant F49620-00-1-0327,
  the California MICRO grant 01-037, the DARPA grant F33615-C-98-3614, the MARCO grant
  98-DT-660, and the NSF grants CCR-0208875, CCR-0085949, and CCR-0225610.
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000−0002−2985−7724
- first_name: Christoph
  full_name: Kirsch, Christoph
  last_name: Kirsch
- first_name: Slobodan
  full_name: Matic, Slobodan
  last_name: Matic
citation:
  ama: 'Henzinger TA, Kirsch C, Matic S. Schedule-carrying code. In: <i>Proceedings
    of the 3rd International Conference on Embedded Software</i>. Vol 2855. ACM; 2003:241-256.
    doi:<a href="https://doi.org/10.1007/978-3-540-45212-6_16">10.1007/978-3-540-45212-6_16</a>'
  apa: 'Henzinger, T. A., Kirsch, C., &#38; Matic, S. (2003). Schedule-carrying code.
    In <i>Proceedings of the 3rd International Conference on Embedded Software</i>
    (Vol. 2855, pp. 241–256). Philadelphia, PA, USA: ACM. <a href="https://doi.org/10.1007/978-3-540-45212-6_16">https://doi.org/10.1007/978-3-540-45212-6_16</a>'
  chicago: Henzinger, Thomas A, Christoph Kirsch, and Slobodan Matic. “Schedule-Carrying
    Code.” In <i>Proceedings of the 3rd International Conference on Embedded Software</i>,
    2855:241–56. ACM, 2003. <a href="https://doi.org/10.1007/978-3-540-45212-6_16">https://doi.org/10.1007/978-3-540-45212-6_16</a>.
  ieee: T. A. Henzinger, C. Kirsch, and S. Matic, “Schedule-carrying code,” in <i>Proceedings
    of the 3rd International Conference on Embedded Software</i>, Philadelphia, PA,
    USA, 2003, vol. 2855, pp. 241–256.
  ista: 'Henzinger TA, Kirsch C, Matic S. 2003. Schedule-carrying code. Proceedings
    of the 3rd International Conference on Embedded Software. EMSOFT: Embedded Software
    , LNCS, vol. 2855, 241–256.'
  mla: Henzinger, Thomas A., et al. “Schedule-Carrying Code.” <i>Proceedings of the
    3rd International Conference on Embedded Software</i>, vol. 2855, ACM, 2003, pp.
    241–56, doi:<a href="https://doi.org/10.1007/978-3-540-45212-6_16">10.1007/978-3-540-45212-6_16</a>.
  short: T.A. Henzinger, C. Kirsch, S. Matic, in:, Proceedings of the 3rd International
    Conference on Embedded Software, ACM, 2003, pp. 241–256.
conference:
  end_date: 2003-10-15
  location: Philadelphia, PA, USA
  name: 'EMSOFT: Embedded Software '
  start_date: 2003-10-13
date_created: 2018-12-11T12:08:59Z
date_published: 2003-09-29T00:00:00Z
date_updated: 2024-01-10T11:33:57Z
day: '29'
doi: 10.1007/978-3-540-45212-6_16
extern: '1'
intvolume: '      2855'
language:
- iso: eng
month: '09'
oa_version: None
page: 241 - 256
publication: Proceedings of the 3rd International Conference on Embedded Software
publication_identifier:
  isbn:
  - '9783540202233'
publication_status: published
publisher: ACM
publist_id: '267'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Schedule-carrying code
type: conference
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 2855
year: '2003'
...
---
_id: '4465'
abstract:
- lang: eng
  text: Giotto is a principled, tool-supported design methodology for implementing
    embedded control systems on platforms of possibly distributed sensors, actuators,
    CPUs, and networks. Giotto is based on the principle that time-triggered task
    invocations plus time-triggered mode switches can form the abstract essence of
    programming real-time control systems. Giotto consists of a programming language
    with a formal semantics, and a retargetable compiler and runtime library. Giotto
    supports the automation of control system design by strictly separating platform-independent
    functionality and timing concerns from platform-dependent scheduling and communication
    issues. The time-triggered predictability of Giotto makes it particularly suitable
    for safety-critical applications with hard real-time constraints. We illustrate
    the platform independence and time-triggered execution of Giotto by coordinating
    a heterogeneous flock of Intel x86 robots and Lego Mindstorms robots.
article_processing_charge: No
author:
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000−0002−2985−7724
- first_name: Benjamin
  full_name: Horowitz, Benjamin
  last_name: Horowitz
- first_name: Christoph
  full_name: Kirsch, Christoph
  last_name: Kirsch
citation:
  ama: 'Henzinger TA, Horowitz B, Kirsch C. Embedded control systems development with
    Giotto. In: <i>Software-Enabled Control: Information Technology for Dynamical
    Systems</i>. Wiley-Blackwell; 2003:123-146. doi:<a href="https://doi.org/10.1002/047172288X.ch8">10.1002/047172288X.ch8</a>'
  apa: 'Henzinger, T. A., Horowitz, B., &#38; Kirsch, C. (2003). Embedded control
    systems development with Giotto. In <i>Software-Enabled Control: Information Technology
    for Dynamical Systems</i> (pp. 123–146). Wiley-Blackwell. <a href="https://doi.org/10.1002/047172288X.ch8">https://doi.org/10.1002/047172288X.ch8</a>'
  chicago: 'Henzinger, Thomas A, Benjamin Horowitz, and Christoph Kirsch. “Embedded
    Control Systems Development with Giotto.” In <i>Software-Enabled Control: Information
    Technology for Dynamical Systems</i>, 123–46. Wiley-Blackwell, 2003. <a href="https://doi.org/10.1002/047172288X.ch8">https://doi.org/10.1002/047172288X.ch8</a>.'
  ieee: 'T. A. Henzinger, B. Horowitz, and C. Kirsch, “Embedded control systems development
    with Giotto,” in <i>Software-Enabled Control: Information Technology for Dynamical
    Systems</i>, Wiley-Blackwell, 2003, pp. 123–146.'
  ista: 'Henzinger TA, Horowitz B, Kirsch C. 2003.Embedded control systems development
    with Giotto. In: Software-Enabled Control: Information Technology for Dynamical
    Systems. , 123–146.'
  mla: 'Henzinger, Thomas A., et al. “Embedded Control Systems Development with Giotto.”
    <i>Software-Enabled Control: Information Technology for Dynamical Systems</i>,
    Wiley-Blackwell, 2003, pp. 123–46, doi:<a href="https://doi.org/10.1002/047172288X.ch8">10.1002/047172288X.ch8</a>.'
  short: 'T.A. Henzinger, B. Horowitz, C. Kirsch, in:, Software-Enabled Control: Information
    Technology for Dynamical Systems, Wiley-Blackwell, 2003, pp. 123–146.'
date_created: 2018-12-11T12:08:59Z
date_published: 2003-05-20T00:00:00Z
date_updated: 2024-01-08T12:24:01Z
day: '20'
doi: 10.1002/047172288X.ch8
extern: '1'
language:
- iso: eng
month: '05'
oa_version: None
page: 123 - 146
publication: 'Software-Enabled Control: Information Technology for Dynamical Systems'
publication_identifier:
  isbn:
  - '9780471234364 '
publication_status: published
publisher: Wiley-Blackwell
publist_id: '262'
quality_controlled: '1'
status: public
title: Embedded control systems development with Giotto
type: book_chapter
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
year: '2003'
...
---
_id: '4466'
abstract:
- lang: eng
  text: One source of complexity in the μ-calculus is its ability to specify an unbounded
    number of switches between universal (AX) and existential (EX) branching modes.
    We therefore study the problems of satisfiability, validity, model checking, and
    implication for the universal and existential fragments of the μ-calculus, in
    which only one branching mode is allowed. The universal fragment is rich enough
    to express most specifications of interest, and therefore improved algorithms
    are of practical importance. We show that while the satisfiability and validity
    problems become indeed simpler for the existential and universal fragments, this
    is, unfortunately, not the case for model checking and implication. We also show
    the corresponding results for the alternationfree fragment of the μ-calculus,
    where no alternations between least and greatest fixed points are allowed. Our
    results imply that efforts to find a polynomial-time model-checking algorithm
    for the μ-calculus can be replaced by efforts to find such an algorithm for the
    universal or existential fragment.
acknowledgement: This work was supported in part by NSF grant CCR-9988172, the AFOSR
  MURI grant F49620-00-1-0327, and a Microsoft Research Fellowship.
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000−0002−2985−7724
- first_name: Orna
  full_name: Kupferman, Orna
  last_name: Kupferman
- first_name: Ritankar
  full_name: Majumdar, Ritankar
  last_name: Majumdar
citation:
  ama: 'Henzinger TA, Kupferman O, Majumdar R. On the universal and existential fragments
    of the mu-calculus. In: <i>Proceedings of the 9th International Conference on
    Tools and Algorithms for the Construction and Analysis of Systems </i>. Vol 2619.
    Springer; 2003:49-64. doi:<a href="https://doi.org/10.1007/3-540-36577-X_5">10.1007/3-540-36577-X_5</a>'
  apa: 'Henzinger, T. A., Kupferman, O., &#38; Majumdar, R. (2003). On the universal
    and existential fragments of the mu-calculus. In <i>Proceedings of the 9th International
    Conference on Tools and Algorithms for the Construction and Analysis of Systems
    </i> (Vol. 2619, pp. 49–64). Warsaw, Poland: Springer. <a href="https://doi.org/10.1007/3-540-36577-X_5">https://doi.org/10.1007/3-540-36577-X_5</a>'
  chicago: Henzinger, Thomas A, Orna Kupferman, and Ritankar Majumdar. “On the Universal
    and Existential Fragments of the Mu-Calculus.” In <i>Proceedings of the 9th International
    Conference on Tools and Algorithms for the Construction and Analysis of Systems
    </i>, 2619:49–64. Springer, 2003. <a href="https://doi.org/10.1007/3-540-36577-X_5">https://doi.org/10.1007/3-540-36577-X_5</a>.
  ieee: T. A. Henzinger, O. Kupferman, and R. Majumdar, “On the universal and existential
    fragments of the mu-calculus,” in <i>Proceedings of the 9th International Conference
    on Tools and Algorithms for the Construction and Analysis of Systems </i>, Warsaw,
    Poland, 2003, vol. 2619, pp. 49–64.
  ista: 'Henzinger TA, Kupferman O, Majumdar R. 2003. On the universal and existential
    fragments of the mu-calculus. Proceedings of the 9th International Conference
    on Tools and Algorithms for the Construction and Analysis of Systems . TACAS:
    Tools and Algorithms for the Construction and Analysis of Systems, LNCS, vol.
    2619, 49–64.'
  mla: Henzinger, Thomas A., et al. “On the Universal and Existential Fragments of
    the Mu-Calculus.” <i>Proceedings of the 9th International Conference on Tools
    and Algorithms for the Construction and Analysis of Systems </i>, vol. 2619, Springer,
    2003, pp. 49–64, doi:<a href="https://doi.org/10.1007/3-540-36577-X_5">10.1007/3-540-36577-X_5</a>.
  short: T.A. Henzinger, O. Kupferman, R. Majumdar, in:, Proceedings of the 9th International
    Conference on Tools and Algorithms for the Construction and Analysis of Systems
    , Springer, 2003, pp. 49–64.
conference:
  end_date: 2003-04-11
  location: Warsaw, Poland
  name: 'TACAS: Tools and Algorithms for the Construction and Analysis of Systems'
  start_date: 2003-04-07
date_created: 2018-12-11T12:08:59Z
date_published: 2003-03-14T00:00:00Z
date_updated: 2024-01-08T13:17:35Z
day: '14'
doi: 10.1007/3-540-36577-X_5
extern: '1'
intvolume: '      2619'
language:
- iso: eng
month: '03'
oa_version: None
page: 49 - 64
publication: 'Proceedings of the 9th International Conference on Tools and Algorithms
  for the Construction and Analysis of Systems '
publication_identifier:
  isbn:
  - '9783540008989'
publication_status: published
publisher: Springer
publist_id: '263'
quality_controlled: '1'
status: public
title: On the universal and existential fragments of the mu-calculus
type: conference
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 2619
year: '2003'
...
---
_id: '4467'
abstract:
- lang: eng
  text: 'BLAST (the Berkeley Lazy Abstraction Software verification Tool) is a verification
    system for checking safety properties of C programs using automatic property-driven
    construction and model checking of software abstractions. Blast implements an
    abstract-model check-refine loop to check for reachability of a specified label
    in the program. The abstract model is built on the fly using predicate abstraction.
    This model is then checked for reachability. If there is no (abstract) path to
    the specified error label, Blast reports that the system is safe and produces
    a succinct proof. Otherwise, it checks if the path is feasible using symbolic
    execution of the program. If the path is feasible, Blast outputs the path as an
    error trace, otherwise, it uses the infeasibility of the path to refine the abstract
    model. Blast short-circuits the loop from abstraction to verification to refinement,
    integrating the three steps tightly through “lazy abstraction” [5]. This integration
    can offer significant advantages in performance by avoiding the repetition of
    work from one iteration of the loop to the next. '
acknowledgement: This work was supported in part by the NSF grants CCR-0085949 and
  CCR-9988172, the DARPA PCES grant F33615-00-C-1693, the MARCO GSRC grant 98-DT-660,
  and a Microsoft Research Fellowship.
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000−0002−2985−7724
- first_name: Ranjit
  full_name: Jhala, Ranjit
  last_name: Jhala
- first_name: Ritankar
  full_name: Majumdar, Ritankar
  last_name: Majumdar
- first_name: Grégoire
  full_name: Sutre, Grégoire
  last_name: Sutre
citation:
  ama: 'Henzinger TA, Jhala R, Majumdar R, Sutre G. Software verification with BLAST.
    In: <i>Proceedings of the 10th International SPIN Workshop </i>. Vol 2648. Springer;
    2003:235-239. doi:<a href="https://doi.org/10.1007/3-540-44829-2_17">10.1007/3-540-44829-2_17</a>'
  apa: 'Henzinger, T. A., Jhala, R., Majumdar, R., &#38; Sutre, G. (2003). Software
    verification with BLAST. In <i>Proceedings of the 10th International SPIN Workshop
    </i> (Vol. 2648, pp. 235–239). Portland, OR, USA: Springer. <a href="https://doi.org/10.1007/3-540-44829-2_17">https://doi.org/10.1007/3-540-44829-2_17</a>'
  chicago: Henzinger, Thomas A, Ranjit Jhala, Ritankar Majumdar, and Grégoire Sutre.
    “Software Verification with BLAST.” In <i>Proceedings of the 10th International
    SPIN Workshop </i>, 2648:235–39. Springer, 2003. <a href="https://doi.org/10.1007/3-540-44829-2_17">https://doi.org/10.1007/3-540-44829-2_17</a>.
  ieee: T. A. Henzinger, R. Jhala, R. Majumdar, and G. Sutre, “Software verification
    with BLAST,” in <i>Proceedings of the 10th International SPIN Workshop </i>, Portland,
    OR, USA, 2003, vol. 2648, pp. 235–239.
  ista: 'Henzinger TA, Jhala R, Majumdar R, Sutre G. 2003. Software verification with
    BLAST. Proceedings of the 10th International SPIN Workshop . SPIN: Model Checking
    Software, LNCS, vol. 2648, 235–239.'
  mla: Henzinger, Thomas A., et al. “Software Verification with BLAST.” <i>Proceedings
    of the 10th International SPIN Workshop </i>, vol. 2648, Springer, 2003, pp. 235–39,
    doi:<a href="https://doi.org/10.1007/3-540-44829-2_17">10.1007/3-540-44829-2_17</a>.
  short: T.A. Henzinger, R. Jhala, R. Majumdar, G. Sutre, in:, Proceedings of the
    10th International SPIN Workshop , Springer, 2003, pp. 235–239.
conference:
  end_date: 2003-05-10
  location: Portland, OR, USA
  name: 'SPIN: Model Checking Software'
  start_date: 2003-05-09
date_created: 2018-12-11T12:09:00Z
date_published: 2003-04-28T00:00:00Z
date_updated: 2024-01-08T14:05:29Z
day: '28'
doi: 10.1007/3-540-44829-2_17
extern: '1'
intvolume: '      2648'
language:
- iso: eng
month: '04'
oa_version: None
page: 235 - 239
publication: 'Proceedings of the 10th International SPIN Workshop '
publication_identifier:
  isbn:
  - '9783540401179'
publication_status: published
publisher: Springer
publist_id: '264'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Software verification with BLAST
type: conference
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 2648
year: '2003'
...
---
_id: '4468'
abstract:
- lang: eng
  text: Giotto is a high-level programming language for time-triggered control applications.
    The authors begin with a conceptual overview of its methodology, discuss the Giotto
    helicopter project, and summarize available Giotto implementations.
acknowledgement: We thank Niklaus Wirth and Walter Schaufelberger for their advice
  and support of the reengineering effort of the ETH Zurich helicopter control system
  using Giotto. This research was supported in part by DARPA SEC grant F33615-C-98–3614,
  MARCO GSRC grant 98-DT-660, and AFOSR MURI grant F49620–00-1–0327. A preliminary
  version of this article appeared as [1].
article_processing_charge: No
article_type: original
author:
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000−0002−2985−7724
- first_name: Christoph
  full_name: Kirsch, Christoph
  last_name: Kirsch
- first_name: Marco
  full_name: Sanvido, Marco
  last_name: Sanvido
- first_name: Wolfgang
  full_name: Pree, Wolfgang
  last_name: Pree
citation:
  ama: Henzinger TA, Kirsch C, Sanvido M, Pree W. From control models to real-time
    code using Giotto. <i>IEEE Control Systems Magazine</i>. 2003;23(1):50-64. doi:<a
    href="https://doi.org/10.1109/MCS.2003.1172829">10.1109/MCS.2003.1172829</a>
  apa: Henzinger, T. A., Kirsch, C., Sanvido, M., &#38; Pree, W. (2003). From control
    models to real-time code using Giotto. <i>IEEE Control Systems Magazine</i>. IEEE.
    <a href="https://doi.org/10.1109/MCS.2003.1172829">https://doi.org/10.1109/MCS.2003.1172829</a>
  chicago: Henzinger, Thomas A, Christoph Kirsch, Marco Sanvido, and Wolfgang Pree.
    “From Control Models to Real-Time Code Using Giotto.” <i>IEEE Control Systems
    Magazine</i>. IEEE, 2003. <a href="https://doi.org/10.1109/MCS.2003.1172829">https://doi.org/10.1109/MCS.2003.1172829</a>.
  ieee: T. A. Henzinger, C. Kirsch, M. Sanvido, and W. Pree, “From control models
    to real-time code using Giotto,” <i>IEEE Control Systems Magazine</i>, vol. 23,
    no. 1. IEEE, pp. 50–64, 2003.
  ista: Henzinger TA, Kirsch C, Sanvido M, Pree W. 2003. From control models to real-time
    code using Giotto. IEEE Control Systems Magazine. 23(1), 50–64.
  mla: Henzinger, Thomas A., et al. “From Control Models to Real-Time Code Using Giotto.”
    <i>IEEE Control Systems Magazine</i>, vol. 23, no. 1, IEEE, 2003, pp. 50–64, doi:<a
    href="https://doi.org/10.1109/MCS.2003.1172829">10.1109/MCS.2003.1172829</a>.
  short: T.A. Henzinger, C. Kirsch, M. Sanvido, W. Pree, IEEE Control Systems Magazine
    23 (2003) 50–64.
date_created: 2018-12-11T12:09:00Z
date_published: 2003-01-29T00:00:00Z
date_updated: 2024-01-08T10:54:53Z
day: '29'
doi: 10.1109/MCS.2003.1172829
extern: '1'
intvolume: '        23'
issue: '1'
language:
- iso: eng
month: '01'
oa_version: None
page: 50 - 64
publication: IEEE Control Systems Magazine
publication_identifier:
  issn:
  - '1066-033X '
publication_status: published
publisher: IEEE
publist_id: '260'
quality_controlled: '1'
scopus_import: '1'
status: public
title: From control models to real-time code using Giotto
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 23
year: '2003'
...
---
_id: '4469'
abstract:
- lang: eng
  text: Giotto provides an abstract programmer's model for the implementation of embedded
    control systems with hard real-time constraints. A typical control application
    consists of periodic software tasks together with a mode-switching logic for enabling
    and disabling tasks. Giotto specifies time-triggered sensor readings, task invocations,
    actuator updates, and mode switches independent of any implementation platform.
    Giotto can be annotated with platform constraints such as task-to-host mappings,
    and task and communication schedules. The annotations are directives for the Giotto
    compiler, but they do not alter the functionality and timing of a Giotto program.
    By separating the platform-independent from the platform-dependent concerns, Giotto
    enables a great deal of flexibility in choosing control platforms as well as a
    great deal of automation in the validation and synthesis of control software.
    The time-triggered nature of Giotto achieves timing predictability, which makes
    Giotto particularly suitable for safety-critical applications.
acknowledgement: The authors would like to thank R. Majumdar for implementing a prototype
  Giotto compiler for Lego Mindstorms robots. They would like to thank D. Derevyanko
  and W. Williams for building the Intel x86 robots; and E. Lee and X. Liu for help
  with implementing Giotto as a “model of computation” in Ptolemy II [26]. Finally,
  they would also like to thank M. Sanvido for his suggestions on the design of the
  Giotto drivers; and P. Griffiths for implementing the functionality code of the
  electronic throttle controller.
article_processing_charge: No
article_type: original
author:
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000−0002−2985−7724
- first_name: Benjamin
  full_name: Horowitz, Benjamin
  last_name: Horowitz
- first_name: Christoph
  full_name: Kirsch, Christoph
  last_name: Kirsch
citation:
  ama: 'Henzinger TA, Horowitz B, Kirsch C. Giotto: A time-triggered language for
    embedded programming. <i>Proceedings of the IEEE</i>. 2003;91(1):84-99. doi:<a
    href="https://doi.org/10.1109/JPROC.2002.805825">10.1109/JPROC.2002.805825</a>'
  apa: 'Henzinger, T. A., Horowitz, B., &#38; Kirsch, C. (2003). Giotto: A time-triggered
    language for embedded programming. <i>Proceedings of the IEEE</i>. IEEE. <a href="https://doi.org/10.1109/JPROC.2002.805825">https://doi.org/10.1109/JPROC.2002.805825</a>'
  chicago: 'Henzinger, Thomas A, Benjamin Horowitz, and Christoph Kirsch. “Giotto:
    A Time-Triggered Language for Embedded Programming.” <i>Proceedings of the IEEE</i>.
    IEEE, 2003. <a href="https://doi.org/10.1109/JPROC.2002.805825">https://doi.org/10.1109/JPROC.2002.805825</a>.'
  ieee: 'T. A. Henzinger, B. Horowitz, and C. Kirsch, “Giotto: A time-triggered language
    for embedded programming,” <i>Proceedings of the IEEE</i>, vol. 91, no. 1. IEEE,
    pp. 84–99, 2003.'
  ista: 'Henzinger TA, Horowitz B, Kirsch C. 2003. Giotto: A time-triggered language
    for embedded programming. Proceedings of the IEEE. 91(1), 84–99.'
  mla: 'Henzinger, Thomas A., et al. “Giotto: A Time-Triggered Language for Embedded
    Programming.” <i>Proceedings of the IEEE</i>, vol. 91, no. 1, IEEE, 2003, pp.
    84–99, doi:<a href="https://doi.org/10.1109/JPROC.2002.805825">10.1109/JPROC.2002.805825</a>.'
  short: T.A. Henzinger, B. Horowitz, C. Kirsch, Proceedings of the IEEE 91 (2003)
    84–99.
date_created: 2018-12-11T12:09:00Z
date_published: 2003-01-29T00:00:00Z
date_updated: 2024-01-10T11:55:18Z
day: '29'
doi: 10.1109/JPROC.2002.805825
extern: '1'
intvolume: '        91'
issue: '1'
language:
- iso: eng
month: '01'
oa_version: None
page: 84 - 99
publication: Proceedings of the IEEE
publication_identifier:
  issn:
  - '0018-9219 '
publication_status: published
publisher: IEEE
publist_id: '261'
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Giotto: A time-triggered language for embedded programming'
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 91
year: '2003'
...
---
_id: '2613'
abstract:
- lang: eng
  text: In this investigation, we report identification and characterization of a
    95 kDa postsynaptic density protein (PSD-95)/discs-large/ ZO-1 (PDZ) domain-containing
    protein termed tamalin, also recently named GRP1-associated scaffold protein (GRASP),
    that interacts with group 1 metabotropic glutamate receptors (mGluRs). The yeast
    two-hybrid system and in vitro pull-down assays indicated that the PDZ domain-containing,
    amino-terminal half of tamalin directly binds to the class I PDZ-binding motif
    of group 1 mGluRs. The C-terminal half of tamalin also bound to cytohesins, the
    members of guanine nucleotide exchange factors (GEFs) specific for the ADP-ribosylation
    factor (ARF) family of small GTP-binding proteins. Tamalin mRNA is expressed predominantly
    in the telencephalic region and highly overlaps with the expression of group 1
    mGluR mRNAs. Both tamalin and cytohesin-2 were enriched and codistributed with
    mGluR1a in postsynaptic membrane fractions. Importantly, recombinant and native
    mGluR1a/tamalin/cytohesin-2 complexes were coimmunoprecipitated from transfected
    COS-7 cells and rat brain tissue, respectively. Transfection of tamalin and mutant
    tamalin lacking a cytohesin-binding domain caused an increase and decrease in
    cell-surface expression of mGluR1a in COS-7 cells, respectively. Furthermore,
    adenovirus-mediated expression of tamalin and dominant-negative tamalin facilitated
    and reduced the neuritic distribution of endogenous mGluR5 in cultured hippocampal
    neurons, respectively. The results indicate that tamalin plays a key role in the
    association of group 1 mGluRs with the ARF-specific GEF proteins and contributes
    to intracellular trafficking and the macromolecular organization of group 1 mGluRs
    at synapses.
acknowledgement: This work was supported in part by research grants from the Ministry
  of Education, Science and Culture of Japan. We thank Bert Vogelstein for providing
  adenoviral recombination vectors and Haruhiko Bito for a gift of the enolase promoter
  and technical advice. We are grateful to Atsushi Nishimune and Satoshi Kaneko for
  technical advice and Kumlesh K. Dev for careful reading of this manuscript.
article_processing_charge: No
article_type: original
author:
- first_name: Jun
  full_name: Kitano, Jun
  last_name: Kitano
- first_name: Kouji
  full_name: Kimura, Kouji
  last_name: Kimura
- first_name: Yoshimitsu
  full_name: Yamazaki, Yoshimitsu
  last_name: Yamazaki
- first_name: Takeshi
  full_name: Soda, Takeshi
  last_name: Soda
- first_name: Ryuichi
  full_name: Shigemoto, Ryuichi
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
- first_name: Yoshiaki
  full_name: Nakajima, Yoshiaki
  last_name: Nakajima
- first_name: Shigetada
  full_name: Nakanishi, Shigetada
  last_name: Nakanishi
citation:
  ama: Kitano J, Kimura K, Yamazaki Y, et al. Tamalin, a PDZ domain-containing protein,
    links a protein complex formation of group 1 metabotropic glutamate receptors
    and the guanine nucleotide exchange factor cytohesins. <i>Journal of Neuroscience</i>.
    2002;22(4):1280-1289. doi:<a href="https://doi.org/10.1523/JNEUROSCI.22-04-01280.2002">10.1523/JNEUROSCI.22-04-01280.2002</a>
  apa: Kitano, J., Kimura, K., Yamazaki, Y., Soda, T., Shigemoto, R., Nakajima, Y.,
    &#38; Nakanishi, S. (2002). Tamalin, a PDZ domain-containing protein, links a
    protein complex formation of group 1 metabotropic glutamate receptors and the
    guanine nucleotide exchange factor cytohesins. <i>Journal of Neuroscience</i>.
    Society for Neuroscience. <a href="https://doi.org/10.1523/JNEUROSCI.22-04-01280.2002">https://doi.org/10.1523/JNEUROSCI.22-04-01280.2002</a>
  chicago: Kitano, Jun, Kouji Kimura, Yoshimitsu Yamazaki, Takeshi Soda, Ryuichi Shigemoto,
    Yoshiaki Nakajima, and Shigetada Nakanishi. “Tamalin, a PDZ Domain-Containing
    Protein, Links a Protein Complex Formation of Group 1 Metabotropic Glutamate Receptors
    and the Guanine Nucleotide Exchange Factor Cytohesins.” <i>Journal of Neuroscience</i>.
    Society for Neuroscience, 2002. <a href="https://doi.org/10.1523/JNEUROSCI.22-04-01280.2002">https://doi.org/10.1523/JNEUROSCI.22-04-01280.2002</a>.
  ieee: J. Kitano <i>et al.</i>, “Tamalin, a PDZ domain-containing protein, links
    a protein complex formation of group 1 metabotropic glutamate receptors and the
    guanine nucleotide exchange factor cytohesins,” <i>Journal of Neuroscience</i>,
    vol. 22, no. 4. Society for Neuroscience, pp. 1280–1289, 2002.
  ista: Kitano J, Kimura K, Yamazaki Y, Soda T, Shigemoto R, Nakajima Y, Nakanishi
    S. 2002. Tamalin, a PDZ domain-containing protein, links a protein complex formation
    of group 1 metabotropic glutamate receptors and the guanine nucleotide exchange
    factor cytohesins. Journal of Neuroscience. 22(4), 1280–1289.
  mla: Kitano, Jun, et al. “Tamalin, a PDZ Domain-Containing Protein, Links a Protein
    Complex Formation of Group 1 Metabotropic Glutamate Receptors and the Guanine
    Nucleotide Exchange Factor Cytohesins.” <i>Journal of Neuroscience</i>, vol. 22,
    no. 4, Society for Neuroscience, 2002, pp. 1280–89, doi:<a href="https://doi.org/10.1523/JNEUROSCI.22-04-01280.2002">10.1523/JNEUROSCI.22-04-01280.2002</a>.
  short: J. Kitano, K. Kimura, Y. Yamazaki, T. Soda, R. Shigemoto, Y. Nakajima, S.
    Nakanishi, Journal of Neuroscience 22 (2002) 1280–1289.
date_created: 2018-12-11T11:58:40Z
date_published: 2002-02-15T00:00:00Z
date_updated: 2023-07-25T11:34:46Z
day: '15'
doi: 10.1523/JNEUROSCI.22-04-01280.2002
extern: '1'
external_id:
  pmid:
  - '11850456'
intvolume: '        22'
issue: '4'
language:
- iso: eng
month: '02'
oa_version: None
page: 1280 - 1289
pmid: 1
publication: Journal of Neuroscience
publication_identifier:
  issn:
  - 0270-6474
publication_status: published
publisher: Society for Neuroscience
publist_id: '4285'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Tamalin, a PDZ domain-containing protein, links a protein complex formation
  of group 1 metabotropic glutamate receptors and the guanine nucleotide exchange
  factor cytohesins
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 22
year: '2002'
...
---
_id: '2614'
abstract:
- lang: eng
  text: Metabotropic glutamate receptors (mGluRs) from group III reduce glutamate
    release. Because these receptors reduce cAMP levels, we explored whether this
    signaling pathway contributes to release inhibition caused by mGluRs with low
    affinity for L-2-amino-4-phosphonobutyrate (L-AP4). In biochemical experiments
    with the population of cerebrocortical nerve terminals we find that L-AP4 (1 mM)
    inhibited the Ca2+dependent-evoked release of glutamate by 25%. This inhibitory
    effect was largely prevented by the pertussis toxin but was insensitive to inhibitors
    of protein kinase C bisindolylmaleimide and protein kinase A H-89. Furthermore,
    this inhibition was associated with reduction in N-type Ca2+ channel activity
    in the absence of any detectable change in cAMP levels. In the presence of forskolin,
    however, L-AP4 decreased the levels of cAMP. The activation of this additional
    signaling pathway was very efficient in counteracting the facilitation of glutamate
    release induced either by forskolin or the β-adrenergic receptor agonist isoproterenol.
    Imaging experiments to measure Ca2+ dynamics in single nerve terminals showed
    that L-AP4 strongly reduced the Ca2+ response in 28% of the nerve terminals. Moreover,
    immunochemical experiments showed that 25-35% of the nerve terminals that were
    immunopositive to synaptophysin were also immunoreactive to the low affinity L-AP4-sensitive
    mGluR7. Then, mGluR7 mediates the inhibition of glutamate release caused by 1
    mM L-AP4, primarily by a strong inhibition of Ca2+ channels, although high cAMP
    uncovers the receptor ability to decrease cAMP.
acknowledgement: We thank Dr. Enrique Castro from Las Palmas University for critical
  reading of the manuscript and M. Sefton for editorial assistance.
article_processing_charge: No
article_type: original
author:
- first_name: Carmelo
  full_name: Millán, Carmelo
  last_name: Millán
- first_name: Rafael
  full_name: Luján, Rafael
  last_name: Luján
- first_name: Ryuichi
  full_name: Shigemoto, Ryuichi
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
- first_name: José
  full_name: Sánchez Prieto, José
  last_name: Sánchez Prieto
citation:
  ama: Millán C, Luján R, Shigemoto R, Sánchez Prieto J. The inhibition of glutamate
    release by metabotropic glutamate receptor 7 affects both [Ca2+]c and cAMP. Evidence
    for a strong reduction of Ca2+ entry in single nerve terminals. <i>Journal of
    Biological Chemistry</i>. 2002;277(16):14092-14101. doi:<a href="https://doi.org/10.1074/jbc.M109044200">10.1074/jbc.M109044200</a>
  apa: Millán, C., Luján, R., Shigemoto, R., &#38; Sánchez Prieto, J. (2002). The
    inhibition of glutamate release by metabotropic glutamate receptor 7 affects both
    [Ca2+]c and cAMP. Evidence for a strong reduction of Ca2+ entry in single nerve
    terminals. <i>Journal of Biological Chemistry</i>. American Society for Biochemistry
    and Molecular Biology. <a href="https://doi.org/10.1074/jbc.M109044200">https://doi.org/10.1074/jbc.M109044200</a>
  chicago: Millán, Carmelo, Rafael Luján, Ryuichi Shigemoto, and José Sánchez Prieto.
    “The Inhibition of Glutamate Release by Metabotropic Glutamate Receptor 7 Affects
    Both [Ca2+]c and CAMP. Evidence for a Strong Reduction of Ca2+ Entry in Single
    Nerve Terminals.” <i>Journal of Biological Chemistry</i>. American Society for
    Biochemistry and Molecular Biology, 2002. <a href="https://doi.org/10.1074/jbc.M109044200">https://doi.org/10.1074/jbc.M109044200</a>.
  ieee: C. Millán, R. Luján, R. Shigemoto, and J. Sánchez Prieto, “The inhibition
    of glutamate release by metabotropic glutamate receptor 7 affects both [Ca2+]c
    and cAMP. Evidence for a strong reduction of Ca2+ entry in single nerve terminals,”
    <i>Journal of Biological Chemistry</i>, vol. 277, no. 16. American Society for
    Biochemistry and Molecular Biology, pp. 14092–14101, 2002.
  ista: Millán C, Luján R, Shigemoto R, Sánchez Prieto J. 2002. The inhibition of
    glutamate release by metabotropic glutamate receptor 7 affects both [Ca2+]c and
    cAMP. Evidence for a strong reduction of Ca2+ entry in single nerve terminals.
    Journal of Biological Chemistry. 277(16), 14092–14101.
  mla: Millán, Carmelo, et al. “The Inhibition of Glutamate Release by Metabotropic
    Glutamate Receptor 7 Affects Both [Ca2+]c and CAMP. Evidence for a Strong Reduction
    of Ca2+ Entry in Single Nerve Terminals.” <i>Journal of Biological Chemistry</i>,
    vol. 277, no. 16, American Society for Biochemistry and Molecular Biology, 2002,
    pp. 14092–101, doi:<a href="https://doi.org/10.1074/jbc.M109044200">10.1074/jbc.M109044200</a>.
  short: C. Millán, R. Luján, R. Shigemoto, J. Sánchez Prieto, Journal of Biological
    Chemistry 277 (2002) 14092–14101.
date_created: 2018-12-11T11:58:41Z
date_published: 2002-04-19T00:00:00Z
date_updated: 2023-07-25T10:16:44Z
day: '19'
ddc:
- '570'
doi: 10.1074/jbc.M109044200
extern: '1'
external_id:
  pmid:
  - '11825890'
file:
- access_level: open_access
  checksum: 0290fcbbd9153ec654185b0c856f214c
  content_type: application/pdf
  creator: alisjak
  date_created: 2023-07-25T10:13:16Z
  date_updated: 2023-07-25T10:13:16Z
  file_id: '13309'
  file_name: 2002_JBC_Millan.pdf
  file_size: 2105520
  relation: main_file
  success: 1
file_date_updated: 2023-07-25T10:13:16Z
has_accepted_license: '1'
intvolume: '       277'
issue: '16'
language:
- iso: eng
license: https://creativecommons.org/licenses/by/4.0/
month: '04'
oa: 1
oa_version: Published Version
page: 14092 - 14101
pmid: 1
publication: Journal of Biological Chemistry
publication_identifier:
  issn:
  - 0021-9258
publication_status: published
publisher: American Society for Biochemistry and Molecular Biology
publist_id: '4284'
quality_controlled: '1'
scopus_import: '1'
status: public
title: The inhibition of glutamate release by metabotropic glutamate receptor 7 affects
  both [Ca2+]c and cAMP. Evidence for a strong reduction of Ca2+ entry in single nerve
  terminals
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 277
year: '2002'
...
---
_id: '2615'
abstract:
- lang: eng
  text: Taste-mGluR4, cloned from taste tissues, is a truncated variant of brain-expressed
    mGluR4a (brain-mGluR4), and is known to be a candidate for the receptor involved
    in the umami taste sense. Although the expression patterns of taste- and brain-mGluR4
    mRNAs have been demonstrated, no mention has so far been made of the expression
    of these two mGluR4 proteins in taste tissues. The present study examined the
    expression of taste-mGluR4 and brain-mGluR4 proteins in rat taste tissues by using
    a specific antibody for mGluR4a which shared a C-terminus of both taste- and brain-mGluR4,
    for immunoblot analysis and immunohistochemistry. Immunoblot analysis showed that
    both brain-mGluR4 and taste-mGluR4 were expressed in the taste tissues. Taste-mGluR4
    was not detected in the cerebellum. The immunoreactive band for brain-mGluR4 protein
    was much stronger than that for taste-mGluR4 protein. In the cryosections of fungiform,
    foliate and circumvallate papillae, the antibody against taste-mGluR4 exhibited
    intense labeling of the taste pores and taste hairs in all the taste buds of gustatory
    papillae examined; the immunoreaction to the antibody against brain-mGluR4 was
    more intense at the same sites of the taste buds. The portions of the taste bud
    cells below the taste pore and surrounding keratinocytes did not show any immunoreactivities.
    The results of the present study strongly suggest that, in addition to taste-mGluR4,
    brain-mGluR4 may function even more importantly than the former as a receptor
    for glutamate, i.e. the umami taste sensation.
article_processing_charge: No
article_type: original
author:
- first_name: Takashi
  full_name: Toyono, Takashi
  last_name: Toyono
- first_name: Yuji
  full_name: Seta, Yuji
  last_name: Seta
- first_name: Shinji
  full_name: Sataoka, Shinji
  last_name: Sataoka
- first_name: Harumi
  full_name: Harada, Harumi
  id: 2E55CDF2-F248-11E8-B48F-1D18A9856A87
  last_name: Harada
  orcid: 0000-0001-7429-7896
- first_name: Takahiko
  full_name: Morotomi, Takahiko
  last_name: Morotomi
- first_name: Shintaro
  full_name: Kawano, Shintaro
  last_name: Kawano
- first_name: Ryuichi
  full_name: Shigemoto, Ryuichi
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
- first_name: Kuniaki
  full_name: Toyoshima, Kuniaki
  last_name: Toyoshima
citation:
  ama: Toyono T, Seta Y, Sataoka S, et al. Expression of the metabotropic glutamate
    receptor, mGluR4a, in the taste hairs of taste buds in rat gustatory papillae.
    <i>Archives of Histology and Cytology</i>. 2002;65(1):91-96. doi:<a href="https://doi.org/10.1679/aohc.65.91">10.1679/aohc.65.91</a>
  apa: Toyono, T., Seta, Y., Sataoka, S., Harada, H., Morotomi, T., Kawano, S., …
    Toyoshima, K. (2002). Expression of the metabotropic glutamate receptor, mGluR4a,
    in the taste hairs of taste buds in rat gustatory papillae. <i>Archives of Histology
    and Cytology</i>. Japan Society of Histological Documentation. <a href="https://doi.org/10.1679/aohc.65.91">https://doi.org/10.1679/aohc.65.91</a>
  chicago: Toyono, Takashi, Yuji Seta, Shinji Sataoka, Harumi Harada, Takahiko Morotomi,
    Shintaro Kawano, Ryuichi Shigemoto, and Kuniaki Toyoshima. “Expression of the
    Metabotropic Glutamate Receptor, MGluR4a, in the Taste Hairs of Taste Buds in
    Rat Gustatory Papillae.” <i>Archives of Histology and Cytology</i>. Japan Society
    of Histological Documentation, 2002. <a href="https://doi.org/10.1679/aohc.65.91">https://doi.org/10.1679/aohc.65.91</a>.
  ieee: T. Toyono <i>et al.</i>, “Expression of the metabotropic glutamate receptor,
    mGluR4a, in the taste hairs of taste buds in rat gustatory papillae,” <i>Archives
    of Histology and Cytology</i>, vol. 65, no. 1. Japan Society of Histological Documentation,
    pp. 91–96, 2002.
  ista: Toyono T, Seta Y, Sataoka S, Harada H, Morotomi T, Kawano S, Shigemoto R,
    Toyoshima K. 2002. Expression of the metabotropic glutamate receptor, mGluR4a,
    in the taste hairs of taste buds in rat gustatory papillae. Archives of Histology
    and Cytology. 65(1), 91–96.
  mla: Toyono, Takashi, et al. “Expression of the Metabotropic Glutamate Receptor,
    MGluR4a, in the Taste Hairs of Taste Buds in Rat Gustatory Papillae.” <i>Archives
    of Histology and Cytology</i>, vol. 65, no. 1, Japan Society of Histological Documentation,
    2002, pp. 91–96, doi:<a href="https://doi.org/10.1679/aohc.65.91">10.1679/aohc.65.91</a>.
  short: T. Toyono, Y. Seta, S. Sataoka, H. Harada, T. Morotomi, S. Kawano, R. Shigemoto,
    K. Toyoshima, Archives of Histology and Cytology 65 (2002) 91–96.
date_created: 2018-12-11T11:58:41Z
date_published: 2002-01-01T00:00:00Z
date_updated: 2023-07-25T10:00:15Z
day: '01'
doi: 10.1679/aohc.65.91
extern: '1'
external_id:
  pmid:
  - '12002614'
intvolume: '        65'
issue: '1'
language:
- iso: eng
month: '01'
oa_version: None
page: 91 - 96
pmid: 1
publication: Archives of Histology and Cytology
publication_identifier:
  issn:
  - 0914-9465
publication_status: published
publisher: Japan Society of Histological Documentation
publist_id: '4283'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Expression of the metabotropic glutamate receptor, mGluR4a, in the taste hairs
  of taste buds in rat gustatory papillae
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 65
year: '2002'
...
---
_id: '2616'
abstract:
- lang: eng
  text: Neurons in the rat cerebral cortex are enriched in group I metabotropic glutamate
    receptor (mGluR) subtypes and respond to their activation during development.
    To understand better the mechanisms by which mGluR1 and mGluR5 mediate these effects,
    the goal of this study was to elucidate the expression pattern and to determine
    the cellular and the precise subcellular localization of these two receptor subtypes
    in the rat neocortex and hippocampus during late prenatal and postnatal development.
    At the light microscopic level, mGluR1 α and mGluR5 were first detected in the
    cerebral cortex with different expression levels at embryonic day E18. Thus, mGluR5
    had a moderate expression, whereas mGluR1 α was detected as a diffuse and weak
    labeling. mGluR5 was localized in some Cajal-Retzius cells as well as in other
    cell types, such as pioneer neurons of the marginal zone. During postnatal development,
    the distribution of the receptors dramatically changed. From P0 to around P10,
    mGluR1α was localized in identified, transient Cajal-Retzius cells of neocortex
    and hippocampus, until these cells disappear. In addition, a population of interneurons
    localized the receptor from the second/third postnatal week. In contrast, mGluR5
    was localized mainly in pyramidal cells and in some interneurons, with a neuropilar
    staining throughout the cerebral cortex. At the electron microscopic level, the
    immunoreactivity for both group I mGluR subtypes was expressed postsynaptically.
    Using immunogold methods, mGluR1α and mGluR5 immunoreactivities were found throughout
    postnatal development at the edge of postsynaptic specialization of asymmetrical
    synapses. These results show that the two group I mGluRs have a differential expression
    pattern in neocortex and hippocampus that may suggest roles for the receptors
    in the early processing of cortical information and in the control of cortical
    developmental events.
acknowledgement: The authors are grateful to Dr Ole Paulsen and Professor Kay Davies
  for their comments on the manuscript. We also would like to thank Dr Zoltan Molnar
  for his support and Mrs Lucy Jones, Ms Courtney Voelker and Mr David Dongworth for
  the English revision of the manuscript. This work was supported by grants from the
  European Community (QLG3-CT-1999-00192 to R.L.) and the Spanish Ministerio de Ciencia
  y Tecnología (PB97-0582-CO2-01 to A.F.).
article_processing_charge: No
article_type: original
author:
- first_name: Guillermina
  full_name: López Bendito, Guillermina
  last_name: López Bendito
- first_name: Ryuichi
  full_name: Shigemoto, Ryuichi
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
- first_name: Alfonso
  full_name: Fairén, Alfonso
  last_name: Fairén
- first_name: Rafael
  full_name: Luján, Rafael
  last_name: Luján
citation:
  ama: López Bendito G, Shigemoto R, Fairén A, Luján R. Differential distribution
    of group I metabotropic glutamate receptors during rat cortical development. <i>Cerebral
    Cortex</i>. 2002;12(6):625-638. doi:<a href="https://doi.org/10.1093/cercor/12.6.625">10.1093/cercor/12.6.625</a>
  apa: López Bendito, G., Shigemoto, R., Fairén, A., &#38; Luján, R. (2002). Differential
    distribution of group I metabotropic glutamate receptors during rat cortical development.
    <i>Cerebral Cortex</i>. Oxford University Press. <a href="https://doi.org/10.1093/cercor/12.6.625">https://doi.org/10.1093/cercor/12.6.625</a>
  chicago: López Bendito, Guillermina, Ryuichi Shigemoto, Alfonso Fairén, and Rafael
    Luján. “Differential Distribution of Group I Metabotropic Glutamate Receptors
    during Rat Cortical Development.” <i>Cerebral Cortex</i>. Oxford University Press,
    2002. <a href="https://doi.org/10.1093/cercor/12.6.625">https://doi.org/10.1093/cercor/12.6.625</a>.
  ieee: G. López Bendito, R. Shigemoto, A. Fairén, and R. Luján, “Differential distribution
    of group I metabotropic glutamate receptors during rat cortical development,”
    <i>Cerebral Cortex</i>, vol. 12, no. 6. Oxford University Press, pp. 625–638,
    2002.
  ista: López Bendito G, Shigemoto R, Fairén A, Luján R. 2002. Differential distribution
    of group I metabotropic glutamate receptors during rat cortical development. Cerebral
    Cortex. 12(6), 625–638.
  mla: López Bendito, Guillermina, et al. “Differential Distribution of Group I Metabotropic
    Glutamate Receptors during Rat Cortical Development.” <i>Cerebral Cortex</i>,
    vol. 12, no. 6, Oxford University Press, 2002, pp. 625–38, doi:<a href="https://doi.org/10.1093/cercor/12.6.625">10.1093/cercor/12.6.625</a>.
  short: G. López Bendito, R. Shigemoto, A. Fairén, R. Luján, Cerebral Cortex 12 (2002)
    625–638.
date_created: 2018-12-11T11:58:41Z
date_published: 2002-06-01T00:00:00Z
date_updated: 2023-07-25T09:54:10Z
day: '01'
doi: 10.1093/cercor/12.6.625
extern: '1'
external_id:
  pmid:
  - '12003862'
intvolume: '        12'
issue: '6'
language:
- iso: eng
month: '06'
oa_version: None
page: 625 - 638
pmid: 1
publication: Cerebral Cortex
publication_identifier:
  issn:
  - 1047-3211
publication_status: published
publisher: Oxford University Press
publist_id: '4282'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Differential distribution of group I metabotropic glutamate receptors during
  rat cortical development
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 12
year: '2002'
...
---
_id: '2617'
abstract:
- lang: eng
  text: Synapses exhibit different short-term plasticity patterns and this behaviour
    influences information processing in neuronal networks. We tested how the short-term
    plasticity of excitatory postsynaptic currents (EPSCs) depends on the postsynaptic
    cell type, identified by axonal arborizations and molecular markers in the hippocampal
    CA1 area. Three distinct types of short-term synaptic behaviour (facilitating,
    depressing and combined facilitating-depressing) were defined by fitting a dynamic
    neurotransmission model to the data. Approximately 75 % of the oriens-lacunosum-moleculare
    (O-LM) interneurones received facilitating EPSCs, but in three of 12 O-LM cells
    EPSCs also showed significant depression. Over 90 % of the O-LM cells were immunopositive
    for somatostatin and mGluR1α and all tested cells were decorated by strongly mGluR7a
    positive axon terminals. Responses in eight of 12 basket cells were described
    well with a model involving only depression, but the other cells displayed combined
    facilitating-depressing EPSCs. No apparent difference was found between the plasticity
    of EPSCs in cholecystokinin- or parvalbumin-containing basket cells. In oriens-bistratified
    cells (O-Bi), two of nine cells showed facilitating EPSCs, another two depressing,
    and the remaining five cells combined facilitating-depressing EPSCs. Seven of
    10 cells tested for somatostatin were immunopositive, but mGluR1α was detectable
    only in two of 11 tested cells. Furthermore, most O-Bi cells projected to the
    CA3 area and the subiculum, as well as outside the hippocampal formation. Postsynaptic
    responses to action potentials recorded in vivo from a CA1 place cell were modelled,
    and revealed great differences between and within cell types. Our results demonstrate
    that the short-term plasticity of EPSCs is cell type dependent, but with significant
    heterogeneity within all three interneurone populations.
author:
- first_name: Attila
  full_name: Losonczy, Attila
  last_name: Losonczy
- first_name: Limei
  full_name: Zhang, Limei
  last_name: Zhang
- first_name: Ryuichi
  full_name: Ryuichi Shigemoto
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
- first_name: Péter
  full_name: Somogyi, Péter
  last_name: Somogyi
- first_name: Zoltán
  full_name: Nusser, Zoltán
  last_name: Nusser
citation:
  ama: Losonczy A, Zhang L, Shigemoto R, Somogyi P, Nusser Z. Cell type dependence
    and variability in the short-term plasticity of EPSCs in identified mouse hippocampal
    interneurones. <i>Journal of Physiology</i>. 2002;542(1):193-210. doi:<a href="https://doi.org/10.1113/jphysiol.2002.020024">10.1113/jphysiol.2002.020024</a>
  apa: Losonczy, A., Zhang, L., Shigemoto, R., Somogyi, P., &#38; Nusser, Z. (2002).
    Cell type dependence and variability in the short-term plasticity of EPSCs in
    identified mouse hippocampal interneurones. <i>Journal of Physiology</i>. Wiley-Blackwell.
    <a href="https://doi.org/10.1113/jphysiol.2002.020024">https://doi.org/10.1113/jphysiol.2002.020024</a>
  chicago: Losonczy, Attila, Limei Zhang, Ryuichi Shigemoto, Péter Somogyi, and Zoltán
    Nusser. “Cell Type Dependence and Variability in the Short-Term Plasticity of
    EPSCs in Identified Mouse Hippocampal Interneurones.” <i>Journal of Physiology</i>.
    Wiley-Blackwell, 2002. <a href="https://doi.org/10.1113/jphysiol.2002.020024">https://doi.org/10.1113/jphysiol.2002.020024</a>.
  ieee: A. Losonczy, L. Zhang, R. Shigemoto, P. Somogyi, and Z. Nusser, “Cell type
    dependence and variability in the short-term plasticity of EPSCs in identified
    mouse hippocampal interneurones,” <i>Journal of Physiology</i>, vol. 542, no.
    1. Wiley-Blackwell, pp. 193–210, 2002.
  ista: Losonczy A, Zhang L, Shigemoto R, Somogyi P, Nusser Z. 2002. Cell type dependence
    and variability in the short-term plasticity of EPSCs in identified mouse hippocampal
    interneurones. Journal of Physiology. 542(1), 193–210.
  mla: Losonczy, Attila, et al. “Cell Type Dependence and Variability in the Short-Term
    Plasticity of EPSCs in Identified Mouse Hippocampal Interneurones.” <i>Journal
    of Physiology</i>, vol. 542, no. 1, Wiley-Blackwell, 2002, pp. 193–210, doi:<a
    href="https://doi.org/10.1113/jphysiol.2002.020024">10.1113/jphysiol.2002.020024</a>.
  short: A. Losonczy, L. Zhang, R. Shigemoto, P. Somogyi, Z. Nusser, Journal of Physiology
    542 (2002) 193–210.
date_created: 2018-12-11T11:58:42Z
date_published: 2002-07-01T00:00:00Z
date_updated: 2021-01-12T06:58:36Z
day: '01'
doi: 10.1113/jphysiol.2002.020024
extern: 1
intvolume: '       542'
issue: '1'
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2290398/
month: '07'
oa: 1
page: 193 - 210
publication: Journal of Physiology
publication_status: published
publisher: Wiley-Blackwell
publist_id: '4281'
quality_controlled: 0
status: public
title: Cell type dependence and variability in the short-term plasticity of EPSCs
  in identified mouse hippocampal interneurones
type: journal_article
volume: 542
year: '2002'
...
---
_id: '2618'
abstract:
- lang: eng
  text: The unipolar brush cell (UBC) is a type of glutamatergic interneuron in the
    granular layer of the cerebellum. The UBC brush and a single mossy fiber (MF)
    terminal contact each other within a cerebellar glomerulus, forming a giant synapse.
    Many UBCs receive input from extrinsic MFs, whereas others are innervated by intrinsic
    mossy terminals formed by the axons of other UBCs. In all mammalian species so
    far examined, the vestibulocerebellum is enriched of UBCs that are strongly immunoreactive
    for the calcium binding protein calretinin (CR) in both the somatodendritic and
    axonal compartment. UBCs have postsynaptic ionotropic glutamate receptors and
    extrasynaptic metabotropic glutamate receptors that immunocytochemically highlight
    their somatodendritic compartment and brush, respectively. In this study on the
    mouse cerebellum, we present evidence that immunoreactivities to CR and mGluR1α
    define two distinct UBC subsets with partly overlapping distributions in lobule
    X (the nodulus). In sections double-labeled for CR and mGluR1α, the patterns of
    distributions of CR+/mGluR1α- UBCs and CR-/mGluR1α+ UBCs differed along the mediolateral
    and dorsoventral axes of the folium. Moreover, mGluR1α+ UBCs outnumbered CR+ UBCs.
    Both UBC subsets were mGluR2/3, GluR2/3, and NMDAR1 immunoreactive. The different
    distribution patterns of the two UBC subsets within lobule X suggest that expression
    of CR or mGluR1α by UBCs may be afferent-specific and related to the terminal
    fields of different vestibular MF afferents.
article_processing_charge: No
article_type: original
author:
- first_name: Maria
  full_name: Nunzi, Maria
  last_name: Nunzi
- first_name: Ryuichi
  full_name: Shigemoto, Ryuichi
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
- first_name: Enrico
  full_name: Mugnaini, Enrico
  last_name: Mugnaini
citation:
  ama: Nunzi M, Shigemoto R, Mugnaini E. Differential expression of calretinin and
    metabotropic glutamate receptor mGluR1α defines subsets of unipolar brush cells
    in mouse cerebellum. <i>Journal of Comparative Neurology</i>. 2002;451(2):189-199.
    doi:<a href="https://doi.org/10.1002/cne.10344">10.1002/cne.10344</a>
  apa: Nunzi, M., Shigemoto, R., &#38; Mugnaini, E. (2002). Differential expression
    of calretinin and metabotropic glutamate receptor mGluR1α defines subsets of unipolar
    brush cells in mouse cerebellum. <i>Journal of Comparative Neurology</i>. Wiley-Blackwell.
    <a href="https://doi.org/10.1002/cne.10344">https://doi.org/10.1002/cne.10344</a>
  chicago: Nunzi, Maria, Ryuichi Shigemoto, and Enrico Mugnaini. “Differential Expression
    of Calretinin and Metabotropic Glutamate Receptor MGluR1α Defines Subsets of Unipolar
    Brush Cells in Mouse Cerebellum.” <i>Journal of Comparative Neurology</i>. Wiley-Blackwell,
    2002. <a href="https://doi.org/10.1002/cne.10344">https://doi.org/10.1002/cne.10344</a>.
  ieee: M. Nunzi, R. Shigemoto, and E. Mugnaini, “Differential expression of calretinin
    and metabotropic glutamate receptor mGluR1α defines subsets of unipolar brush
    cells in mouse cerebellum,” <i>Journal of Comparative Neurology</i>, vol. 451,
    no. 2. Wiley-Blackwell, pp. 189–199, 2002.
  ista: Nunzi M, Shigemoto R, Mugnaini E. 2002. Differential expression of calretinin
    and metabotropic glutamate receptor mGluR1α defines subsets of unipolar brush
    cells in mouse cerebellum. Journal of Comparative Neurology. 451(2), 189–199.
  mla: Nunzi, Maria, et al. “Differential Expression of Calretinin and Metabotropic
    Glutamate Receptor MGluR1α Defines Subsets of Unipolar Brush Cells in Mouse Cerebellum.”
    <i>Journal of Comparative Neurology</i>, vol. 451, no. 2, Wiley-Blackwell, 2002,
    pp. 189–99, doi:<a href="https://doi.org/10.1002/cne.10344">10.1002/cne.10344</a>.
  short: M. Nunzi, R. Shigemoto, E. Mugnaini, Journal of Comparative Neurology 451
    (2002) 189–199.
date_created: 2018-12-11T11:58:42Z
date_published: 2002-09-16T00:00:00Z
date_updated: 2023-07-25T09:09:48Z
day: '16'
doi: 10.1002/cne.10344
extern: '1'
external_id:
  pmid:
  - '12209836'
intvolume: '       451'
issue: '2'
language:
- iso: eng
month: '09'
oa_version: None
page: 189 - 199
pmid: 1
publication: Journal of Comparative Neurology
publication_identifier:
  issn:
  - 0021-9967
publication_status: published
publisher: Wiley-Blackwell
publist_id: '4279'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Differential expression of calretinin and metabotropic glutamate receptor mGluR1α
  defines subsets of unipolar brush cells in mouse cerebellum
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 451
year: '2002'
...
---
_id: '2619'
abstract:
- lang: eng
  text: The release of glutamate and GABA is modulated by presynaptic metabotropic
    glutamate receptors (mGluRs). We used immunocytochemical methods to define the
    location of the group III receptor mGluR7a in glutamatergic and GABAergic terminals
    innervating GABAergic interneurons and pyramidal cells. Immunoreactivity for mGluR7a
    was localized in the presynaptic active zone of both identified GABAergic and
    presumed glutamatergic terminals. Terminals innervating dendritic spines showed
    a variable level of receptor immunoreactivity, ranging from immunonegative to
    strongly immunopositive. The frequency of strongly mGluR7a positive terminals
    innervating the soma and dendrites of mGluR1α/somatostatin-expressing interneurons
    was very high relative to other neurons. On dendrites that received mGluR7a-enriched
    glutamatergic innervation, at least 80% of GABAergic terminals were immunopositive
    for mGluR7a. On such dendrites virtually all (95%) vasoactive intestinal polypeptide
    (VIP) positive (GABAergic) terminals were enriched in mGluR7a. The targets of
    VIP/mGluR7a-expressing terminals were mainly (88%) mGluR1α-expressing interneurons,
    which were mostly somatostatin immunopositive. Parvalbumin positive terminals
    were immunonegative for mGluR7a. Some parvalbumin immunoreactive dendrites received
    strongly mGluR7a positive terminals. The subcellular location, as well as the
    cell type and synapse-specific distribution of mGluR7a in isocortical neuronal
    circuits, is homologous to its distribution in the hippocampus. The specific location
    of mGluR7a in the presynaptic active zone of both glutamatergic and GABAergic
    synapses may be related to the proximity of calcium channels and the vesicle fusion
    machinery. The enrichment of mGluR7a in the main GABAergic, as well as in the
    glutamatergic, innervation of mGluR1α/somatostatin-expressing interneurons suggests
    that their activation is under unique regulation by extracellular glutamate.
acknowledgement: We thank Dr C. Paspalas for an initial contribution to the immunocytochemistry.
  We are grateful for the generous gifts of antibodies from Dr A. Buchan (anti-somatostatin,
  Department of Physiology, University of British Columbia, Canada), Dr M. Watanabe
  (anti-mGluR1α, Department of Anatomy, Hokkaido University School of Medicine, Sapporo)
  and Dr K. Tanaka (anti-GAD, Niigata University, Faculty of Medicine, Department
  of Neurology). We thank Dr F. Ferraguti for helpful suggestions during the project
  and for his comments on a previous version of the manuscript. We also thank Philip
  Cobden, Paul Jays and Laszlo Marton for assistance. Y.D. was supported by a Wellcome
  Trust Advanced Training Fellowship.
article_processing_charge: No
article_type: original
author:
- first_name: Yannis
  full_name: Dalezios, Yannis
  last_name: Dalezios
- first_name: Rafael
  full_name: Luján, Rafael
  last_name: Luján
- first_name: Ryuichi
  full_name: Shigemoto, Ryuichi
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
- first_name: John
  full_name: Roberts, John
  last_name: Roberts
- first_name: Péter
  full_name: Somogyi, Péter
  last_name: Somogyi
citation:
  ama: Dalezios Y, Luján R, Shigemoto R, Roberts J, Somogyi P. Enrichment of mGluR7a
    in the Presynaptic active zones of GABAergic and Non-GABAergic terminals on interneurons
    in the rat somatosensory cortex. <i>Cerebral Cortex</i>. 2002;12(9):961-974. doi:<a
    href="https://doi.org/10.1093/cercor/12.9.961">10.1093/cercor/12.9.961</a>
  apa: Dalezios, Y., Luján, R., Shigemoto, R., Roberts, J., &#38; Somogyi, P. (2002).
    Enrichment of mGluR7a in the Presynaptic active zones of GABAergic and Non-GABAergic
    terminals on interneurons in the rat somatosensory cortex. <i>Cerebral Cortex</i>.
    Oxford University Press. <a href="https://doi.org/10.1093/cercor/12.9.961">https://doi.org/10.1093/cercor/12.9.961</a>
  chicago: Dalezios, Yannis, Rafael Luján, Ryuichi Shigemoto, John Roberts, and Péter
    Somogyi. “Enrichment of MGluR7a in the Presynaptic Active Zones of GABAergic and
    Non-GABAergic Terminals on Interneurons in the Rat Somatosensory Cortex.” <i>Cerebral
    Cortex</i>. Oxford University Press, 2002. <a href="https://doi.org/10.1093/cercor/12.9.961">https://doi.org/10.1093/cercor/12.9.961</a>.
  ieee: Y. Dalezios, R. Luján, R. Shigemoto, J. Roberts, and P. Somogyi, “Enrichment
    of mGluR7a in the Presynaptic active zones of GABAergic and Non-GABAergic terminals
    on interneurons in the rat somatosensory cortex,” <i>Cerebral Cortex</i>, vol.
    12, no. 9. Oxford University Press, pp. 961–974, 2002.
  ista: Dalezios Y, Luján R, Shigemoto R, Roberts J, Somogyi P. 2002. Enrichment of
    mGluR7a in the Presynaptic active zones of GABAergic and Non-GABAergic terminals
    on interneurons in the rat somatosensory cortex. Cerebral Cortex. 12(9), 961–974.
  mla: Dalezios, Yannis, et al. “Enrichment of MGluR7a in the Presynaptic Active Zones
    of GABAergic and Non-GABAergic Terminals on Interneurons in the Rat Somatosensory
    Cortex.” <i>Cerebral Cortex</i>, vol. 12, no. 9, Oxford University Press, 2002,
    pp. 961–74, doi:<a href="https://doi.org/10.1093/cercor/12.9.961">10.1093/cercor/12.9.961</a>.
  short: Y. Dalezios, R. Luján, R. Shigemoto, J. Roberts, P. Somogyi, Cerebral Cortex
    12 (2002) 961–974.
date_created: 2018-12-11T11:58:42Z
date_published: 2002-09-01T00:00:00Z
date_updated: 2023-07-25T09:40:49Z
day: '01'
doi: 10.1093/cercor/12.9.961
extern: '1'
external_id:
  pmid:
  - '12183395'
intvolume: '        12'
issue: '9'
language:
- iso: eng
month: '09'
oa_version: None
page: 961 - 974
pmid: 1
publication: Cerebral Cortex
publication_identifier:
  issn:
  - 1047-3211
publication_status: published
publisher: Oxford University Press
publist_id: '4280'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Enrichment of mGluR7a in the Presynaptic active zones of GABAergic and Non-GABAergic
  terminals on interneurons in the rat somatosensory cortex
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 12
year: '2002'
...
---
_id: '2620'
abstract:
- lang: eng
  text: An ion channel's function depends largely on its location and density on neurons.
    Here we used high-resolution immunolocalization to determine the subcellular distribution
    of the hyperpolarization-activated and cyclic-nucleotide-gated channel subunit
    1 (HCN1) in rat brain. Light microscopy revealed graded HCN1 immunoreactivity
    in apical dendrites of hippocampal, subicular and neocortical layer-5 pyramidal
    cells. Quantitative comparison of immunogold densities showed a 60-fold increase
    from somatic to distal apical dendritic membranes. Distal dendritic shafts had
    16 times more HCN1 labeling than proximal dendrites of similar diameters. At the
    same distance from the soma, the density of HCN1 was significantly higher in dendritic
    shafts than in spines. Our results reveal the complex cell surface distribution
    of voltage-gated ion-channels, and predict its role in increasing the computational
    power of single neurons via subcellular domain and input-specific mechanisms.
acknowledgement: Z.N. received grants from the Hungarian Science Foundation (T032309),
  the Howard Hughes Medical Institute, the James S. McDonnell Foundation, the Wellcome
  Trust and the Boehringer Ingelheim Fund. Z.N. and R.S. received grants from CREST—Japan
  Science and Technology Corporation. G.T. is funded by the Wellcome Trust.
article_processing_charge: No
article_type: original
author:
- first_name: Andrea
  full_name: Lörincz, Andrea
  last_name: Lörincz
- first_name: Takuya
  full_name: Notomi, Takuya
  last_name: Notomi
- first_name: Gábor
  full_name: Tamás, Gábor
  last_name: Tamás
- first_name: Ryuichi
  full_name: Shigemoto, Ryuichi
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
- first_name: Zoltán
  full_name: Nusser, Zoltán
  last_name: Nusser
citation:
  ama: Lörincz A, Notomi T, Tamás G, Shigemoto R, Nusser Z. Polarized and compartment-dependent
    distribution of HCN1 in pyramidal cell dendrites. <i>Nature Neuroscience</i>.
    2002;5(11):1185-1193. doi:<a href="https://doi.org/10.1038/nn962">10.1038/nn962</a>
  apa: Lörincz, A., Notomi, T., Tamás, G., Shigemoto, R., &#38; Nusser, Z. (2002).
    Polarized and compartment-dependent distribution of HCN1 in pyramidal cell dendrites.
    <i>Nature Neuroscience</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/nn962">https://doi.org/10.1038/nn962</a>
  chicago: Lörincz, Andrea, Takuya Notomi, Gábor Tamás, Ryuichi Shigemoto, and Zoltán
    Nusser. “Polarized and Compartment-Dependent Distribution of HCN1 in Pyramidal
    Cell Dendrites.” <i>Nature Neuroscience</i>. Nature Publishing Group, 2002. <a
    href="https://doi.org/10.1038/nn962">https://doi.org/10.1038/nn962</a>.
  ieee: A. Lörincz, T. Notomi, G. Tamás, R. Shigemoto, and Z. Nusser, “Polarized and
    compartment-dependent distribution of HCN1 in pyramidal cell dendrites,” <i>Nature
    Neuroscience</i>, vol. 5, no. 11. Nature Publishing Group, pp. 1185–1193, 2002.
  ista: Lörincz A, Notomi T, Tamás G, Shigemoto R, Nusser Z. 2002. Polarized and compartment-dependent
    distribution of HCN1 in pyramidal cell dendrites. Nature Neuroscience. 5(11),
    1185–1193.
  mla: Lörincz, Andrea, et al. “Polarized and Compartment-Dependent Distribution of
    HCN1 in Pyramidal Cell Dendrites.” <i>Nature Neuroscience</i>, vol. 5, no. 11,
    Nature Publishing Group, 2002, pp. 1185–93, doi:<a href="https://doi.org/10.1038/nn962">10.1038/nn962</a>.
  short: A. Lörincz, T. Notomi, G. Tamás, R. Shigemoto, Z. Nusser, Nature Neuroscience
    5 (2002) 1185–1193.
date_created: 2018-12-11T11:58:43Z
date_published: 2002-11-01T00:00:00Z
date_updated: 2023-07-25T09:02:48Z
day: '01'
doi: 10.1038/nn962
extern: '1'
external_id:
  pmid:
  - '12389030'
intvolume: '         5'
issue: '11'
language:
- iso: eng
month: '11'
oa_version: None
page: 1185 - 1193
pmid: 1
publication: Nature Neuroscience
publication_identifier:
  issn:
  - 1097-6256
publication_status: published
publisher: Nature Publishing Group
publist_id: '4278'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Polarized and compartment-dependent distribution of HCN1 in pyramidal cell
  dendrites
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 5
year: '2002'
...
---
_id: '2621'
abstract:
- lang: eng
  text: The release properties of glutamatergic nerve terminals are influenced by
    a number of factors, including the subtype of voltage-dependent calcium channel
    and the presence of presynaptic autoreceptors. Group III metabotropic glutamate
    receptors (mGluRs) mediate feedback inhibition of glutamate release by inhibiting
    Ca2+ channel activity. By imaging Ca2+ in preparations of cerebrocortical nerve
    terminals, we show that voltage-dependent Ca2+ channels are distributed in a heterogeneous
    manner in individual nerve terminals. Presynaptic terminals contained only N-type
    (47.5%; conotoxin GVIA-sensitive), P/Q-type (3.9%; agatoxin IVA-sensitive), or
    both N- and P/Q-type (42.6%) Ca2+ channels, although the remainder of the terminals
    (6.1%) were insensitive to these two toxins. In this preparation, two mGluRs with
    high and low affinity for L(+)-2-amino-4-phosphonobutyrate were identified by
    immunocytochemistry as mGluR4 and mGluR7, respectively. These receptors were responsible
    for 22.2 and 24.1% reduction of glutamate release, and they reduced the Ca2+ response
    in 24.4 and 30.3% of the nerve terminals, respectively. Interestingly, mGluR4
    was largely (73.7%) located in nerve terminals expressing both N- and P/Q-type
    Ca2+ channels, whereas mGluR7 was predominantly (69.9%) located in N-type Ca2+
    channel-expressing terminals. This specific coexpression of different group III
    mGluRs and Ca2+ channels may endow synaptic terminals with distinct release properties
    and reveals the existence of a high degree of presynaptic heterogeneity.
acknowledgement: We thank M. Sefton for editorial assistance.
article_processing_charge: No
article_type: original
author:
- first_name: Carmelo
  full_name: Millán, Carmelo
  last_name: Millán
- first_name: Rafael
  full_name: Luján, Rafael
  last_name: Luján
- first_name: Ryuichi
  full_name: Shigemoto, Ryuichi
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
- first_name: José
  full_name: Sánchez Prieto, José
  last_name: Sánchez Prieto
citation:
  ama: Millán C, Luján R, Shigemoto R, Sánchez Prieto J. Subtype-specific expression
    of Group III metabotropic glutamate receptors and Ca2+ channels in single nerve
    terminals. <i>Journal of Biological Chemistry</i>. 2002;277(49):47796-47803. doi:<a
    href="https://doi.org/10.1074/jbc.M207531200">10.1074/jbc.M207531200</a>
  apa: Millán, C., Luján, R., Shigemoto, R., &#38; Sánchez Prieto, J. (2002). Subtype-specific
    expression of Group III metabotropic glutamate receptors and Ca2+ channels in
    single nerve terminals. <i>Journal of Biological Chemistry</i>. American Society
    for Biochemistry and Molecular Biology. <a href="https://doi.org/10.1074/jbc.M207531200">https://doi.org/10.1074/jbc.M207531200</a>
  chicago: Millán, Carmelo, Rafael Luján, Ryuichi Shigemoto, and José Sánchez Prieto.
    “Subtype-Specific Expression of Group III Metabotropic Glutamate Receptors and
    Ca2+ Channels in Single Nerve Terminals.” <i>Journal of Biological Chemistry</i>.
    American Society for Biochemistry and Molecular Biology, 2002. <a href="https://doi.org/10.1074/jbc.M207531200">https://doi.org/10.1074/jbc.M207531200</a>.
  ieee: C. Millán, R. Luján, R. Shigemoto, and J. Sánchez Prieto, “Subtype-specific
    expression of Group III metabotropic glutamate receptors and Ca2+ channels in
    single nerve terminals,” <i>Journal of Biological Chemistry</i>, vol. 277, no.
    49. American Society for Biochemistry and Molecular Biology, pp. 47796–47803,
    2002.
  ista: Millán C, Luján R, Shigemoto R, Sánchez Prieto J. 2002. Subtype-specific expression
    of Group III metabotropic glutamate receptors and Ca2+ channels in single nerve
    terminals. Journal of Biological Chemistry. 277(49), 47796–47803.
  mla: Millán, Carmelo, et al. “Subtype-Specific Expression of Group III Metabotropic
    Glutamate Receptors and Ca2+ Channels in Single Nerve Terminals.” <i>Journal of
    Biological Chemistry</i>, vol. 277, no. 49, American Society for Biochemistry
    and Molecular Biology, 2002, pp. 47796–803, doi:<a href="https://doi.org/10.1074/jbc.M207531200">10.1074/jbc.M207531200</a>.
  short: C. Millán, R. Luján, R. Shigemoto, J. Sánchez Prieto, Journal of Biological
    Chemistry 277 (2002) 47796–47803.
date_created: 2018-12-11T11:58:43Z
date_published: 2002-12-02T00:00:00Z
date_updated: 2023-07-19T07:49:19Z
day: '02'
doi: 10.1074/jbc.M207531200
extern: '1'
external_id:
  pmid:
  - '12376542'
intvolume: '       277'
issue: '49'
language:
- iso: eng
month: '12'
oa_version: Published Version
page: 47796 - 47803
pmid: 1
publication: Journal of Biological Chemistry
publication_identifier:
  issn:
  - 0021-9258
publication_status: published
publisher: American Society for Biochemistry and Molecular Biology
publist_id: '4277'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Subtype-specific expression of Group III metabotropic glutamate receptors and
  Ca2+ channels in single nerve terminals
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 277
year: '2002'
...
---
_id: '2622'
abstract:
- lang: eng
  text: To understand the possible contribution of metabotropic γ-aminobutyric acid
    receptors (GABABR) in cortical development, we investigated the expression pattern
    and the cellular and subcellular localization of the GABABR1 and GABABR2 subtypes
    in the rat neocortex from embryonic day 14 (E14) to adulthood. At the light microscopic
    level, both GABABR1 and GABABR2 were detected as early as E14. During prenatal
    development, both subtypes were expressed highly in the cortical plate. Using
    double immunofluorescence, GABABR1 colocalized with GABABR2 in neurons of the
    marginal zone and subplate, indicating that these proteins are coexpressed and
    could be forming functional GABABRs during prenatal development in vivo. In contrast,
    only GABABR1 but not GABABR2 was detected in the tangentially migratory cells
    in the lower intermediate zone. During postnatal development, immunoreactivity
    for GABABR1 and GABABR2 was distributed mainly in pyramidal cells. Discrete GABABR1-immunopositive
    cell bodies of interneurons were present throughout the neocortex. In addition,
    GABABR1 but not GABABR2 was found in identified Cajal-Retzius cells in layer I.
    At the electron microscopic level, immunoreactivity for GABABR1 and GABABR2 was
    found in dendritic spines and dendritic shafts at extrasynaptic and perisynaptic
    sites throughout postnatal development. We further demonstrated the presynaptic
    localization of GABABR1 and GABABR2, as well as the association of the receptors
    with asymmetrical synaptic junctions. These results indicate potentially important
    roles for the GABABRs in the regulation of migratory processes during corticogenesis
    and in the modulation of synaptic transmission during early development of cortical
    circuitry.
acknowledgement: The authors are grateful to Dr Marco Sassoe-Pogneto for his comments
  on a previous version of the manuscript. We also would like to thank to Ms. Courtney
  Voelker for the English revision and comments of the manuscript. This work was made
  possible by grants from the European Community (QLG3-CT-1999–00192, R.L) and the
  Spanish Ministry of Science and Technology (PB97-0582-CO2-01, A.F).
article_processing_charge: No
article_type: original
author:
- first_name: Guillermina
  full_name: López Bendito, Guillermina
  last_name: López Bendito
- first_name: Ryuichi
  full_name: Shigemoto, Ryuichi
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
- first_name: Ákos
  full_name: Kulik, Ákos
  last_name: Kulik
- first_name: Ole
  full_name: Paulsen, Ole
  last_name: Paulsen
- first_name: Alfonso
  full_name: Fairén, Alfonso
  last_name: Fairén
- first_name: Rafael
  full_name: Luján, Rafael
  last_name: Luján
citation:
  ama: López Bendito G, Shigemoto R, Kulik Á, Paulsen O, Fairén A, Luján R. Expression
    and distribution of metabotropic GABA receptor subtypes GABABR1 and GABABR2 during
    rat neocortical development. <i>European Journal of Neuroscience</i>. 2002;15(11):1766-1778.
    doi:<a href="https://doi.org/10.1046/j.1460-9568.2002.02032.x">10.1046/j.1460-9568.2002.02032.x</a>
  apa: López Bendito, G., Shigemoto, R., Kulik, Á., Paulsen, O., Fairén, A., &#38;
    Luján, R. (2002). Expression and distribution of metabotropic GABA receptor subtypes
    GABABR1 and GABABR2 during rat neocortical development. <i>European Journal of
    Neuroscience</i>. Wiley-Blackwell. <a href="https://doi.org/10.1046/j.1460-9568.2002.02032.x">https://doi.org/10.1046/j.1460-9568.2002.02032.x</a>
  chicago: López Bendito, Guillermina, Ryuichi Shigemoto, Ákos Kulik, Ole Paulsen,
    Alfonso Fairén, and Rafael Luján. “Expression and Distribution of Metabotropic
    GABA Receptor Subtypes GABABR1 and GABABR2 during Rat Neocortical Development.”
    <i>European Journal of Neuroscience</i>. Wiley-Blackwell, 2002. <a href="https://doi.org/10.1046/j.1460-9568.2002.02032.x">https://doi.org/10.1046/j.1460-9568.2002.02032.x</a>.
  ieee: G. López Bendito, R. Shigemoto, Á. Kulik, O. Paulsen, A. Fairén, and R. Luján,
    “Expression and distribution of metabotropic GABA receptor subtypes GABABR1 and
    GABABR2 during rat neocortical development,” <i>European Journal of Neuroscience</i>,
    vol. 15, no. 11. Wiley-Blackwell, pp. 1766–1778, 2002.
  ista: López Bendito G, Shigemoto R, Kulik Á, Paulsen O, Fairén A, Luján R. 2002.
    Expression and distribution of metabotropic GABA receptor subtypes GABABR1 and
    GABABR2 during rat neocortical development. European Journal of Neuroscience.
    15(11), 1766–1778.
  mla: López Bendito, Guillermina, et al. “Expression and Distribution of Metabotropic
    GABA Receptor Subtypes GABABR1 and GABABR2 during Rat Neocortical Development.”
    <i>European Journal of Neuroscience</i>, vol. 15, no. 11, Wiley-Blackwell, 2002,
    pp. 1766–78, doi:<a href="https://doi.org/10.1046/j.1460-9568.2002.02032.x">10.1046/j.1460-9568.2002.02032.x</a>.
  short: G. López Bendito, R. Shigemoto, Á. Kulik, O. Paulsen, A. Fairén, R. Luján,
    European Journal of Neuroscience 15 (2002) 1766–1778.
date_created: 2018-12-11T11:58:43Z
date_published: 2002-06-01T00:00:00Z
date_updated: 2023-07-19T07:30:39Z
day: '01'
doi: 10.1046/j.1460-9568.2002.02032.x
extern: '1'
external_id:
  pmid:
  - '12081656'
intvolume: '        15'
issue: '11'
language:
- iso: eng
month: '06'
oa_version: None
page: 1766 - 1778
pmid: 1
publication: European Journal of Neuroscience
publication_identifier:
  issn:
  - 0953-816X
publication_status: published
publisher: Wiley-Blackwell
publist_id: '4276'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Expression and distribution of metabotropic GABA receptor subtypes GABABR1
  and GABABR2 during rat neocortical development
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 15
year: '2002'
...
