---
_id: '11478'
abstract:
- lang: eng
  text: Cerebral organoids differentiated from human-induced pluripotent stem cells
    (hiPSC) provide a unique opportunity to investigate brain development. However,
    organoids usually lack microglia, brain-resident immune cells, which are present
    in the early embryonic brain and participate in neuronal circuit development.
    Here, we find IBA1+ microglia-like cells alongside retinal cups between week 3
    and 4 in 2.5D culture with an unguided retinal organoid differentiation protocol.
    Microglia do not infiltrate the neuroectoderm and instead enrich within non-pigmented,
    3D-cystic compartments that develop in parallel to the 3D-retinal organoids. When
    we guide the retinal organoid differentiation with low-dosed BMP4, we prevent
    cup development and enhance microglia and 3D-cysts formation. Mass spectrometry
    identifies these 3D-cysts to express mesenchymal and epithelial markers. We confirmed
    this microglia-preferred environment also within the unguided protocol, providing
    insight into microglial behavior and migration and offer a model to study how
    they enter and distribute within the human brain.
acknowledged_ssus:
- _id: Bio
- _id: LifeSc
acknowledgement: We thank the scientific service units at ISTA, specifically the lab
  support facility and imaging & optics facility for their support; Nicolas Armel
  for performing the Mass Spectrometry. We thank Alexandra Lang and Tanja Peilnsteiner
  for their help in human brain tissue collection, Rouven Schulz for his insights
  into the functional assays We thank all members of the Siegert group for constant
  feedback on the project and Margaret Maes, Rouven Schulz, and Marco Benevento for
  feedback on the manuscript. This project has received funding from the European
  Research Council (ERC) under the European Union’s Horizon 2020 research and innovation
  program (grant No. 715571 to S.S.) and from the Gesellschaft für Forschungsförderung
  Niederösterreich (grant No. Sc19-017 to V.H.).
article_number: '104580'
article_processing_charge: Yes
article_type: original
author:
- first_name: Katarina
  full_name: Bartalska, Katarina
  id: 4D883232-F248-11E8-B48F-1D18A9856A87
  last_name: Bartalska
- first_name: Verena
  full_name: Hübschmann, Verena
  id: 32B7C918-F248-11E8-B48F-1D18A9856A87
  last_name: Hübschmann
- first_name: Medina
  full_name: Korkut, Medina
  id: 4B51CE74-F248-11E8-B48F-1D18A9856A87
  last_name: Korkut
  orcid: 0000-0003-4309-2251
- first_name: Ryan J
  full_name: Cubero, Ryan J
  id: 850B2E12-9CD4-11E9-837F-E719E6697425
  last_name: Cubero
  orcid: 0000-0003-0002-1867
- first_name: Alessandro
  full_name: Venturino, Alessandro
  id: 41CB84B2-F248-11E8-B48F-1D18A9856A87
  last_name: Venturino
  orcid: 0000-0003-2356-9403
- first_name: Karl
  full_name: Rössler, Karl
  last_name: Rössler
- first_name: Thomas
  full_name: Czech, Thomas
  last_name: Czech
- first_name: Sandra
  full_name: Siegert, Sandra
  id: 36ACD32E-F248-11E8-B48F-1D18A9856A87
  last_name: Siegert
  orcid: 0000-0001-8635-0877
citation:
  ama: Bartalska K, Hübschmann V, Korkut M, et al. A systematic characterization of
    microglia-like cell occurrence during retinal organoid differentiation. <i>iScience</i>.
    2022;25(7). doi:<a href="https://doi.org/10.1016/j.isci.2022.104580">10.1016/j.isci.2022.104580</a>
  apa: Bartalska, K., Hübschmann, V., Korkut, M., Cubero, R. J., Venturino, A., Rössler,
    K., … Siegert, S. (2022). A systematic characterization of microglia-like cell
    occurrence during retinal organoid differentiation. <i>IScience</i>. Elsevier.
    <a href="https://doi.org/10.1016/j.isci.2022.104580">https://doi.org/10.1016/j.isci.2022.104580</a>
  chicago: Bartalska, Katarina, Verena Hübschmann, Medina Korkut, Ryan J Cubero, Alessandro
    Venturino, Karl Rössler, Thomas Czech, and Sandra Siegert. “A Systematic Characterization
    of Microglia-like Cell Occurrence during Retinal Organoid Differentiation.” <i>IScience</i>.
    Elsevier, 2022. <a href="https://doi.org/10.1016/j.isci.2022.104580">https://doi.org/10.1016/j.isci.2022.104580</a>.
  ieee: K. Bartalska <i>et al.</i>, “A systematic characterization of microglia-like
    cell occurrence during retinal organoid differentiation,” <i>iScience</i>, vol.
    25, no. 7. Elsevier, 2022.
  ista: Bartalska K, Hübschmann V, Korkut M, Cubero RJ, Venturino A, Rössler K, Czech
    T, Siegert S. 2022. A systematic characterization of microglia-like cell occurrence
    during retinal organoid differentiation. iScience. 25(7), 104580.
  mla: Bartalska, Katarina, et al. “A Systematic Characterization of Microglia-like
    Cell Occurrence during Retinal Organoid Differentiation.” <i>IScience</i>, vol.
    25, no. 7, 104580, Elsevier, 2022, doi:<a href="https://doi.org/10.1016/j.isci.2022.104580">10.1016/j.isci.2022.104580</a>.
  short: K. Bartalska, V. Hübschmann, M. Korkut, R.J. Cubero, A. Venturino, K. Rössler,
    T. Czech, S. Siegert, IScience 25 (2022).
date_created: 2022-07-03T22:01:33Z
date_published: 2022-07-15T00:00:00Z
date_updated: 2023-11-02T12:21:33Z
day: '15'
ddc:
- '610'
department:
- _id: SaSi
doi: 10.1016/j.isci.2022.104580
ec_funded: 1
external_id:
  isi:
  - '000830428500005'
file:
- access_level: open_access
  checksum: a470b74e1b3796c710189c81a4cd4329
  content_type: application/pdf
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  date_created: 2022-07-04T08:19:25Z
  date_updated: 2022-07-04T08:19:25Z
  file_id: '11480'
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file_date_updated: 2022-07-04T08:19:25Z
has_accepted_license: '1'
intvolume: '        25'
isi: 1
issue: '7'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
project:
- _id: 25D4A630-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '715571'
  name: Microglia action towards neuronal circuit formation and function in health
    and disease
- _id: B67AFEDC-15C9-11EA-A837-991A96BB2854
  name: IST Austria Open Access Fund
- _id: 9B99D380-BA93-11EA-9121-9846C619BF3A
  grant_number: SC19-017
  name: How human microglia shape developing neurons during health and inflammation
publication: iScience
publication_identifier:
  eissn:
  - 2589-0042
publication_status: published
publisher: Elsevier
quality_controlled: '1'
related_material:
  record:
  - id: '12117'
    relation: other
    status: public
scopus_import: '1'
status: public
title: A systematic characterization of microglia-like cell occurrence during retinal
  organoid differentiation
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: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 25
year: '2022'
...
---
_id: '12117'
abstract:
- lang: eng
  text: "To understand how potential gene manipulations affect in vitro microglia,
    we provide a set of short protocols to evaluate microglia identity and function.
    We detail steps for immunostaining to determine microglia identity. We describe
    three functional assays for microglia: phagocytosis, calcium response following
    ATP stimulation, and cytokine expression upon inflammatory stimuli. We apply these
    protocols to human induced-pluripotent-stem-cell (hiPSC)-derived microglia, but
    they can be also applied to other in vitro microglial models including primary
    mouse microglia.\r\nFor complete details on the use and execution of this protocol,
    please refer to Bartalska et al. (2022).1"
acknowledged_ssus:
- _id: Bio
acknowledgement: This project has received funding from the European Research Council
  (ERC) under the European Union’s Horizon 2020 research and innovation program (grant
  No. 715571 to S.S.) and from the Gesellschaft für Forschungsförderung Niederösterreich
  (grant No. Sc19-017 to V.H.). We thank Rouven Schulz and Alessandro Venturino for
  their insights into functional assays and data analysis, Verena Seiboth for insights
  into necessary institutional permission, and ISTA imaging & optics facility (IOF)
  especially Bernhard Hochreiter for their support.
article_number: '101866'
article_processing_charge: No
article_type: letter_note
author:
- first_name: Verena
  full_name: Hübschmann, Verena
  id: 32B7C918-F248-11E8-B48F-1D18A9856A87
  last_name: Hübschmann
- first_name: Medina
  full_name: Korkut, Medina
  id: 4B51CE74-F248-11E8-B48F-1D18A9856A87
  last_name: Korkut
  orcid: 0000-0003-4309-2251
- first_name: Sandra
  full_name: Siegert, Sandra
  id: 36ACD32E-F248-11E8-B48F-1D18A9856A87
  last_name: Siegert
  orcid: 0000-0001-8635-0877
citation:
  ama: Hübschmann V, Korkut M, Siegert S. Assessing human iPSC-derived microglia identity
    and function by immunostaining, phagocytosis, calcium activity, and inflammation
    assay. <i>STAR Protocols</i>. 2022;3(4). doi:<a href="https://doi.org/10.1016/j.xpro.2022.101866">10.1016/j.xpro.2022.101866</a>
  apa: Hübschmann, V., Korkut, M., &#38; Siegert, S. (2022). Assessing human iPSC-derived
    microglia identity and function by immunostaining, phagocytosis, calcium activity,
    and inflammation assay. <i>STAR Protocols</i>. Elsevier. <a href="https://doi.org/10.1016/j.xpro.2022.101866">https://doi.org/10.1016/j.xpro.2022.101866</a>
  chicago: Hübschmann, Verena, Medina Korkut, and Sandra Siegert. “Assessing Human
    IPSC-Derived Microglia Identity and Function by Immunostaining, Phagocytosis,
    Calcium Activity, and Inflammation Assay.” <i>STAR Protocols</i>. Elsevier, 2022.
    <a href="https://doi.org/10.1016/j.xpro.2022.101866">https://doi.org/10.1016/j.xpro.2022.101866</a>.
  ieee: V. Hübschmann, M. Korkut, and S. Siegert, “Assessing human iPSC-derived microglia
    identity and function by immunostaining, phagocytosis, calcium activity, and inflammation
    assay,” <i>STAR Protocols</i>, vol. 3, no. 4. Elsevier, 2022.
  ista: Hübschmann V, Korkut M, Siegert S. 2022. Assessing human iPSC-derived microglia
    identity and function by immunostaining, phagocytosis, calcium activity, and inflammation
    assay. STAR Protocols. 3(4), 101866.
  mla: Hübschmann, Verena, et al. “Assessing Human IPSC-Derived Microglia Identity
    and Function by Immunostaining, Phagocytosis, Calcium Activity, and Inflammation
    Assay.” <i>STAR Protocols</i>, vol. 3, no. 4, 101866, Elsevier, 2022, doi:<a href="https://doi.org/10.1016/j.xpro.2022.101866">10.1016/j.xpro.2022.101866</a>.
  short: V. Hübschmann, M. Korkut, S. Siegert, STAR Protocols 3 (2022).
date_created: 2023-01-12T11:56:38Z
date_published: 2022-12-16T00:00:00Z
date_updated: 2023-11-02T12:21:32Z
day: '16'
ddc:
- '570'
department:
- _id: SaSi
- _id: GradSch
doi: 10.1016/j.xpro.2022.101866
ec_funded: 1
file:
- access_level: open_access
  checksum: 3c71b8a60633d42c2f77c49025d5559b
  content_type: application/pdf
  creator: dernst
  date_created: 2023-01-23T09:50:51Z
  date_updated: 2023-01-23T09:50:51Z
  file_id: '12340'
  file_name: 2022_STARProtocols_Huebschmann.pdf
  file_size: 6251945
  relation: main_file
  success: 1
file_date_updated: 2023-01-23T09:50:51Z
has_accepted_license: '1'
intvolume: '         3'
issue: '4'
keyword:
- General Immunology and Microbiology
- General Biochemistry
- Genetics and Molecular Biology
- General Neuroscience
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
project:
- _id: 25D4A630-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '715571'
  name: Microglia action towards neuronal circuit formation and function in health
    and disease
- _id: 9B99D380-BA93-11EA-9121-9846C619BF3A
  grant_number: SC19-017
  name: How human microglia shape developing neurons during health and inflammation
publication: STAR Protocols
publication_identifier:
  issn:
  - 2666-1667
publication_status: published
publisher: Elsevier
quality_controlled: '1'
related_material:
  record:
  - id: '11478'
    relation: other
    status: public
scopus_import: '1'
status: public
title: Assessing human iPSC-derived microglia identity and function by immunostaining,
  phagocytosis, calcium activity, and inflammation assay
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 3
year: '2022'
...
---
_id: '12244'
abstract:
- lang: eng
  text: Environmental cues influence the highly dynamic morphology of microglia. Strategies
    to characterize these changes usually involve user-selected morphometric features,
    which preclude the identification of a spectrum of context-dependent morphological
    phenotypes. Here we develop MorphOMICs, a topological data analysis approach,
    which enables semiautomatic mapping of microglial morphology into an atlas of
    cue-dependent phenotypes and overcomes feature-selection biases and biological
    variability. We extract spatially heterogeneous and sexually dimorphic morphological
    phenotypes for seven adult mouse brain regions. This sex-specific phenotype declines
    with maturation but increases over the disease trajectories in two neurodegeneration
    mouse models, with females showing a faster morphological shift in affected brain
    regions. Remarkably, microglia morphologies reflect an adaptation upon repeated
    exposure to ketamine anesthesia and do not recover to control morphologies. Finally,
    we demonstrate that both long primary processes and short terminal processes provide
    distinct insights to morphological phenotypes. MorphOMICs opens a new perspective
    to characterize microglial morphology.
acknowledged_ssus:
- _id: PreCl
- _id: Bio
- _id: ScienComp
acknowledgement: We thank the scientific service units at ISTA, in particular M. Schunn’s
  team at the preclinical facility, and especially our colony manager S. Haslinger,
  for excellent support. We are also grateful to the ISTA Imaging & Optics Facility,
  and in particular C. Sommer for helping with the data file conversions. We thank
  R. Erhart from the ISTA Scientific Computing Unit for improving the script performance.
  We thank M. Maes, B. Nagy, S. Oakeley and M. Benevento and all members of the Siegert
  group for constant feedback on the project and on the manuscript. This research
  was supported by the European Union Horizon 2020 research and innovation program
  under the Marie Skłodowska-Curie Actions program (754411 to R.J.A.C.), and by the
  European Research Council (grant no. 715571 to S.S.). L.K. was supported by funding
  to the Blue Brain Project, a research center of the École polytechnique fédérale
  de Lausanne, from the Swiss government’s ETH Board of the Swiss Federal Institutes
  of Technology. L.-H.T. was supported by NIH (grant no. R37NS051874) and by the JPB
  Foundation. The funders had no role in study design, data collection and analysis,
  decision to publish or preparation of the manuscript.
article_processing_charge: No
article_type: original
author:
- first_name: Gloria
  full_name: Colombo, Gloria
  id: 3483CF6C-F248-11E8-B48F-1D18A9856A87
  last_name: Colombo
  orcid: 0000-0001-9434-8902
- first_name: Ryan J
  full_name: Cubero, Ryan J
  id: 850B2E12-9CD4-11E9-837F-E719E6697425
  last_name: Cubero
  orcid: 0000-0003-0002-1867
- first_name: Lida
  full_name: Kanari, Lida
  last_name: Kanari
- first_name: Alessandro
  full_name: Venturino, Alessandro
  id: 41CB84B2-F248-11E8-B48F-1D18A9856A87
  last_name: Venturino
  orcid: 0000-0003-2356-9403
- first_name: Rouven
  full_name: Schulz, Rouven
  id: 4C5E7B96-F248-11E8-B48F-1D18A9856A87
  last_name: Schulz
  orcid: 0000-0001-5297-733X
- first_name: Martina
  full_name: Scolamiero, Martina
  last_name: Scolamiero
- first_name: Jens
  full_name: Agerberg, Jens
  last_name: Agerberg
- first_name: Hansruedi
  full_name: Mathys, Hansruedi
  last_name: Mathys
- first_name: Li-Huei
  full_name: Tsai, Li-Huei
  last_name: Tsai
- first_name: Wojciech
  full_name: Chachólski, Wojciech
  last_name: Chachólski
- first_name: Kathryn
  full_name: Hess, Kathryn
  last_name: Hess
- first_name: Sandra
  full_name: Siegert, Sandra
  id: 36ACD32E-F248-11E8-B48F-1D18A9856A87
  last_name: Siegert
  orcid: 0000-0001-8635-0877
citation:
  ama: Colombo G, Cubero RJ, Kanari L, et al. A tool for mapping microglial morphology,
    morphOMICs, reveals brain-region and sex-dependent phenotypes. <i>Nature Neuroscience</i>.
    2022;25(10):1379-1393. doi:<a href="https://doi.org/10.1038/s41593-022-01167-6">10.1038/s41593-022-01167-6</a>
  apa: Colombo, G., Cubero, R. J., Kanari, L., Venturino, A., Schulz, R., Scolamiero,
    M., … Siegert, S. (2022). A tool for mapping microglial morphology, morphOMICs,
    reveals brain-region and sex-dependent phenotypes. <i>Nature Neuroscience</i>.
    Springer Nature. <a href="https://doi.org/10.1038/s41593-022-01167-6">https://doi.org/10.1038/s41593-022-01167-6</a>
  chicago: Colombo, Gloria, Ryan J Cubero, Lida Kanari, Alessandro Venturino, Rouven
    Schulz, Martina Scolamiero, Jens Agerberg, et al. “A Tool for Mapping Microglial
    Morphology, MorphOMICs, Reveals Brain-Region and Sex-Dependent Phenotypes.” <i>Nature
    Neuroscience</i>. Springer Nature, 2022. <a href="https://doi.org/10.1038/s41593-022-01167-6">https://doi.org/10.1038/s41593-022-01167-6</a>.
  ieee: G. Colombo <i>et al.</i>, “A tool for mapping microglial morphology, morphOMICs,
    reveals brain-region and sex-dependent phenotypes,” <i>Nature Neuroscience</i>,
    vol. 25, no. 10. Springer Nature, pp. 1379–1393, 2022.
  ista: Colombo G, Cubero RJ, Kanari L, Venturino A, Schulz R, Scolamiero M, Agerberg
    J, Mathys H, Tsai L-H, Chachólski W, Hess K, Siegert S. 2022. A tool for mapping
    microglial morphology, morphOMICs, reveals brain-region and sex-dependent phenotypes.
    Nature Neuroscience. 25(10), 1379–1393.
  mla: Colombo, Gloria, et al. “A Tool for Mapping Microglial Morphology, MorphOMICs,
    Reveals Brain-Region and Sex-Dependent Phenotypes.” <i>Nature Neuroscience</i>,
    vol. 25, no. 10, Springer Nature, 2022, pp. 1379–93, doi:<a href="https://doi.org/10.1038/s41593-022-01167-6">10.1038/s41593-022-01167-6</a>.
  short: G. Colombo, R.J. Cubero, L. Kanari, A. Venturino, R. Schulz, M. Scolamiero,
    J. Agerberg, H. Mathys, L.-H. Tsai, W. Chachólski, K. Hess, S. Siegert, Nature
    Neuroscience 25 (2022) 1379–1393.
date_created: 2023-01-16T09:53:07Z
date_published: 2022-10-01T00:00:00Z
date_updated: 2024-03-25T23:30:10Z
day: '01'
ddc:
- '570'
department:
- _id: SaSi
doi: 10.1038/s41593-022-01167-6
ec_funded: 1
external_id:
  isi:
  - '000862214700001'
  pmid:
  - '36180790'
file:
- access_level: open_access
  checksum: 28431146873096f52e0107b534f178c9
  content_type: application/pdf
  creator: dernst
  date_created: 2023-01-30T08:06:56Z
  date_updated: 2023-01-30T08:06:56Z
  file_id: '12437'
  file_name: 2022_NatureNeuroscience_Colombo.pdf
  file_size: 23789835
  relation: main_file
  success: 1
file_date_updated: 2023-01-30T08:06:56Z
has_accepted_license: '1'
intvolume: '        25'
isi: 1
issue: '10'
keyword:
- General Neuroscience
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
page: 1379-1393
pmid: 1
project:
- _id: 260C2330-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '754411'
  name: ISTplus - Postdoctoral Fellowships
- _id: 25D4A630-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '715571'
  name: Microglia action towards neuronal circuit formation and function in health
    and disease
publication: Nature Neuroscience
publication_identifier:
  eissn:
  - 1546-1726
  issn:
  - 1097-6256
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
  link:
  - description: News on ISTA website
    relation: press_release
    url: https://ista.ac.at/en/news/morphomics-revealing-the-hidden-meaning-of-microglia-shape/
  record:
  - id: '12378'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: A tool for mapping microglial morphology, morphOMICs, reveals brain-region
  and sex-dependent phenotypes
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: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 25
year: '2022'
...
---
_id: '9642'
abstract:
- lang: eng
  text: Perineuronal nets (PNNs), components of the extracellular matrix, preferentially
    coat parvalbumin-positive interneurons and constrain critical-period plasticity
    in the adult cerebral cortex. Current strategies to remove PNN are long-lasting,
    invasive, and trigger neuropsychiatric symptoms. Here, we apply repeated anesthetic
    ketamine as a method with minimal behavioral effect. We find that this paradigm
    strongly reduces PNN coating in the healthy adult brain and promotes juvenile-like
    plasticity. Microglia are critically involved in PNN loss because they engage
    with parvalbumin-positive neurons in their defined cortical layer. We identify
    external 60-Hz light-flickering entrainment to recapitulate microglia-mediated
    PNN removal. Importantly, 40-Hz frequency, which is known to remove amyloid plaques,
    does not induce PNN loss, suggesting microglia might functionally tune to distinct
    brain frequencies. Thus, our 60-Hz light-entrainment strategy provides an alternative
    form of PNN intervention in the healthy adult brain.
acknowledged_ssus:
- _id: Bio
- _id: PreCl
acknowledgement: We thank the scientific service units at IST Austria, especially
  the IST bioimaging facility, the preclinical facility, and, specifically, Michael
  Schunn and Sonja Haslinger for excellent support; Plexxikon for the PLX food; the
  Csicsvari group for advice and equipment for in vivo recording; Jürgen Siegert for
  the light-entrainment design; Marco Benevento, Soledad Gonzalo Cogno, Pat King,
  and all Siegert group members for constant feedback on the project and manuscript;
  Lorena Pantano (PILM Bioinformatics Core) for assisting with sample-size determination
  for OD plasticity experiments; and Ana Morello from MIT for technical assistance
  with VEPs recordings. This research was supported by a DOC Fellowship from the Austrian
  Academy of Sciences at the Institute of Science and Technology Austria to R.S.,
  from the European Union Horizon 2020 research and innovation program under the Marie
  Skłodowska-Curie Actions program (grants 665385 to G.C.; 754411 to R.J.A.C.), the
  European Research Council (grant 715571 to S.S.), and the National Eye Institute
  of the National Institutes of Health under award numbers R01EY029245 (to M.F.B.)
  and R01EY023037 (diversity supplement to H.D.J-C.).
article_number: '109313'
article_processing_charge: No
article_type: original
author:
- first_name: Alessandro
  full_name: Venturino, Alessandro
  id: 41CB84B2-F248-11E8-B48F-1D18A9856A87
  last_name: Venturino
  orcid: 0000-0003-2356-9403
- first_name: Rouven
  full_name: Schulz, Rouven
  id: 4C5E7B96-F248-11E8-B48F-1D18A9856A87
  last_name: Schulz
  orcid: 0000-0001-5297-733X
- first_name: Héctor
  full_name: De Jesús-Cortés, Héctor
  last_name: De Jesús-Cortés
- first_name: Margaret E
  full_name: Maes, Margaret E
  id: 3838F452-F248-11E8-B48F-1D18A9856A87
  last_name: Maes
  orcid: 0000-0001-9642-1085
- first_name: Balint
  full_name: Nagy, Balint
  id: 93C65ECC-A6F2-11E9-8DF9-9712E6697425
  last_name: Nagy
- first_name: Francis
  full_name: Reilly-Andújar, Francis
  last_name: Reilly-Andújar
- first_name: Gloria
  full_name: Colombo, Gloria
  id: 3483CF6C-F248-11E8-B48F-1D18A9856A87
  last_name: Colombo
  orcid: 0000-0001-9434-8902
- first_name: Ryan J
  full_name: Cubero, Ryan J
  id: 850B2E12-9CD4-11E9-837F-E719E6697425
  last_name: Cubero
  orcid: 0000-0003-0002-1867
- first_name: Florianne E
  full_name: Schoot Uiterkamp, Florianne E
  id: 3526230C-F248-11E8-B48F-1D18A9856A87
  last_name: Schoot Uiterkamp
- first_name: Mark F.
  full_name: Bear, Mark F.
  last_name: Bear
- first_name: Sandra
  full_name: Siegert, Sandra
  id: 36ACD32E-F248-11E8-B48F-1D18A9856A87
  last_name: Siegert
  orcid: 0000-0001-8635-0877
citation:
  ama: Venturino A, Schulz R, De Jesús-Cortés H, et al. Microglia enable mature perineuronal
    nets disassembly upon anesthetic ketamine exposure or 60-Hz light entrainment
    in the healthy brain. <i>Cell Reports</i>. 2021;36(1). doi:<a href="https://doi.org/10.1016/j.celrep.2021.109313">10.1016/j.celrep.2021.109313</a>
  apa: Venturino, A., Schulz, R., De Jesús-Cortés, H., Maes, M. E., Nagy, B., Reilly-Andújar,
    F., … Siegert, S. (2021). Microglia enable mature perineuronal nets disassembly
    upon anesthetic ketamine exposure or 60-Hz light entrainment in the healthy brain.
    <i>Cell Reports</i>. Elsevier. <a href="https://doi.org/10.1016/j.celrep.2021.109313">https://doi.org/10.1016/j.celrep.2021.109313</a>
  chicago: Venturino, Alessandro, Rouven Schulz, Héctor De Jesús-Cortés, Margaret
    E Maes, Balint Nagy, Francis Reilly-Andújar, Gloria Colombo, et al. “Microglia
    Enable Mature Perineuronal Nets Disassembly upon Anesthetic Ketamine Exposure
    or 60-Hz Light Entrainment in the Healthy Brain.” <i>Cell Reports</i>. Elsevier,
    2021. <a href="https://doi.org/10.1016/j.celrep.2021.109313">https://doi.org/10.1016/j.celrep.2021.109313</a>.
  ieee: A. Venturino <i>et al.</i>, “Microglia enable mature perineuronal nets disassembly
    upon anesthetic ketamine exposure or 60-Hz light entrainment in the healthy brain,”
    <i>Cell Reports</i>, vol. 36, no. 1. Elsevier, 2021.
  ista: Venturino A, Schulz R, De Jesús-Cortés H, Maes ME, Nagy B, Reilly-Andújar
    F, Colombo G, Cubero RJ, Schoot Uiterkamp FE, Bear MF, Siegert S. 2021. Microglia
    enable mature perineuronal nets disassembly upon anesthetic ketamine exposure
    or 60-Hz light entrainment in the healthy brain. Cell Reports. 36(1), 109313.
  mla: Venturino, Alessandro, et al. “Microglia Enable Mature Perineuronal Nets Disassembly
    upon Anesthetic Ketamine Exposure or 60-Hz Light Entrainment in the Healthy Brain.”
    <i>Cell Reports</i>, vol. 36, no. 1, 109313, Elsevier, 2021, doi:<a href="https://doi.org/10.1016/j.celrep.2021.109313">10.1016/j.celrep.2021.109313</a>.
  short: A. Venturino, R. Schulz, H. De Jesús-Cortés, M.E. Maes, B. Nagy, F. Reilly-Andújar,
    G. Colombo, R.J. Cubero, F.E. Schoot Uiterkamp, M.F. Bear, S. Siegert, Cell Reports
    36 (2021).
date_created: 2021-07-11T22:01:16Z
date_published: 2021-07-06T00:00:00Z
date_updated: 2023-08-10T14:09:39Z
day: '06'
ddc:
- '570'
department:
- _id: SaSi
doi: 10.1016/j.celrep.2021.109313
ec_funded: 1
external_id:
  isi:
  - '000670188500004'
  pmid:
  - '34233180'
file:
- access_level: open_access
  checksum: f056255f6d01fd9a86b5387635928173
  content_type: application/pdf
  creator: cziletti
  date_created: 2021-07-19T13:32:17Z
  date_updated: 2021-07-19T13:32:17Z
  file_id: '9693'
  file_name: 2021_CellReports_Venturino.pdf
  file_size: 56388540
  relation: main_file
  success: 1
file_date_updated: 2021-07-19T13:32:17Z
has_accepted_license: '1'
intvolume: '        36'
isi: 1
issue: '1'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
- _id: 260C2330-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '754411'
  name: ISTplus - Postdoctoral Fellowships
- _id: 25D4A630-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '715571'
  name: Microglia action towards neuronal circuit formation and function in health
    and disease
publication: Cell Reports
publication_identifier:
  eissn:
  - '22111247'
publication_status: published
publisher: Elsevier
quality_controlled: '1'
related_material:
  link:
  - description: News on IST Homepage
    relation: press_release
    url: https://ist.ac.at/en/news/the-twinkle-and-the-brain/
scopus_import: '1'
status: public
title: Microglia enable mature perineuronal nets disassembly upon anesthetic ketamine
  exposure or 60-Hz light entrainment in the healthy brain
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: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 36
year: '2021'
...
---
_id: '10565'
abstract:
- lang: eng
  text: 'Enzymatic digestion of the extracellular matrix with chondroitinase-ABC reinstates
    juvenile-like plasticity in the adult cortex as it also disassembles the perineuronal
    nets (PNNs). The disadvantage of the enzyme is that it must be applied intracerebrally
    and it degrades the ECM for several weeks. Here, we provide two minimally invasive
    and transient protocols for microglia-enabled PNN disassembly in mouse cortex:
    repeated treatment with ketamine-xylazine-acepromazine (KXA) anesthesia and 60-Hz
    light entrainment. We also discuss how to analyze PNNs within microglial endosomes-lysosomes.
    For complete details on the use and execution of this protocol, please refer to
    Venturino et al. (2021).'
acknowledged_ssus:
- _id: Bio
acknowledgement: This research was supported by the European Research Council (grant
  715571 to S.S.). We thank Rouven Schulz, Michael Schunn, Claudia Gold, Gabriel Krens,
  Sarah Gorkiewicz, Margaret Maes, Jürgen Siegert, Marco Benevento, and Sara Oakeley
  for comments on the manuscript and the IST Austria Bioimaging Facility for the technical
  support.
article_number: '101012'
article_processing_charge: Yes
article_type: original
author:
- first_name: Alessandro
  full_name: Venturino, Alessandro
  id: 41CB84B2-F248-11E8-B48F-1D18A9856A87
  last_name: Venturino
  orcid: 0000-0003-2356-9403
- first_name: Sandra
  full_name: Siegert, Sandra
  id: 36ACD32E-F248-11E8-B48F-1D18A9856A87
  last_name: Siegert
  orcid: 0000-0001-8635-0877
citation:
  ama: Venturino A, Siegert S. Minimally invasive protocols and quantification for
    microglia-mediated perineuronal net disassembly in mouse brain. <i>STAR Protocols</i>.
    2021;2(4). doi:<a href="https://doi.org/10.1016/j.xpro.2021.101012">10.1016/j.xpro.2021.101012</a>
  apa: Venturino, A., &#38; Siegert, S. (2021). Minimally invasive protocols and quantification
    for microglia-mediated perineuronal net disassembly in mouse brain. <i>STAR Protocols</i>.
    Elsevier ; Cell Press. <a href="https://doi.org/10.1016/j.xpro.2021.101012">https://doi.org/10.1016/j.xpro.2021.101012</a>
  chicago: Venturino, Alessandro, and Sandra Siegert. “Minimally Invasive Protocols
    and Quantification for Microglia-Mediated Perineuronal Net Disassembly in Mouse
    Brain.” <i>STAR Protocols</i>. Elsevier ; Cell Press, 2021. <a href="https://doi.org/10.1016/j.xpro.2021.101012">https://doi.org/10.1016/j.xpro.2021.101012</a>.
  ieee: A. Venturino and S. Siegert, “Minimally invasive protocols and quantification
    for microglia-mediated perineuronal net disassembly in mouse brain,” <i>STAR Protocols</i>,
    vol. 2, no. 4. Elsevier ; Cell Press, 2021.
  ista: Venturino A, Siegert S. 2021. Minimally invasive protocols and quantification
    for microglia-mediated perineuronal net disassembly in mouse brain. STAR Protocols.
    2(4), 101012.
  mla: Venturino, Alessandro, and Sandra Siegert. “Minimally Invasive Protocols and
    Quantification for Microglia-Mediated Perineuronal Net Disassembly in Mouse Brain.”
    <i>STAR Protocols</i>, vol. 2, no. 4, 101012, Elsevier ; Cell Press, 2021, doi:<a
    href="https://doi.org/10.1016/j.xpro.2021.101012">10.1016/j.xpro.2021.101012</a>.
  short: A. Venturino, S. Siegert, STAR Protocols 2 (2021).
date_created: 2021-12-19T23:01:32Z
date_published: 2021-12-17T00:00:00Z
date_updated: 2023-11-16T13:11:04Z
day: '17'
ddc:
- '573'
department:
- _id: SaSi
doi: 10.1016/j.xpro.2021.101012
ec_funded: 1
file:
- access_level: open_access
  checksum: 9ea2501056c5df99e84726b845e9b976
  content_type: application/pdf
  creator: cchlebak
  date_created: 2021-12-20T08:58:40Z
  date_updated: 2021-12-20T08:58:40Z
  file_id: '10570'
  file_name: 2021_STARProt_Venturino.pdf
  file_size: 6207060
  relation: main_file
  success: 1
file_date_updated: 2021-12-20T08:58:40Z
has_accepted_license: '1'
intvolume: '         2'
issue: '4'
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
project:
- _id: 25D4A630-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '715571'
  name: Microglia action towards neuronal circuit formation and function in health
    and disease
publication: STAR Protocols
publication_identifier:
  eissn:
  - 2666-1667
publication_status: published
publisher: Elsevier ; Cell Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Minimally invasive protocols and quantification for microglia-mediated perineuronal
  net disassembly in mouse brain
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: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 2
year: '2021'
...
---
_id: '10655'
abstract:
- lang: eng
  text: "Adeno-associated viruses (AAVs) are widely used to deliver genetic material
    in vivo to distinct cell types such as neurons or glial cells, allowing for targeted
    manipulation. Transduction of microglia is mostly excluded from this strategy,
    likely due to the cells’ heterogeneous state upon environmental changes, which
    makes AAV design challenging. Here, we established the retina as a model system
    for microglial AAV validation and optimization. First, we show that AAV2/6 transduced
    microglia in both synaptic layers, where layer preference corresponds to the intravitreal
    or subretinal delivery method. Surprisingly, we observed significantly enhanced
    microglial transduction during photoreceptor degeneration. Thus, we modified the
    AAV6 capsid to reduce heparin binding by introducing four point mutations (K531E,
    R576Q, K493S, and K459S), resulting in increased microglial transduction in the
    outer plexiform layer. Finally, to improve microglial-specific transduction, we
    validated a Cre-dependent transgene delivery cassette for use in combination with
    the Cx3cr1CreERT2 mouse line. Together, our results provide a foundation for future
    studies optimizing AAV-mediated microglia transduction and highlight that environmental
    conditions influence microglial transduction efficiency.\r\n"
acknowledged_ssus:
- _id: Bio
- _id: LifeSc
- _id: PreCl
acknowledgement: This project has received funding from the European Research Council
  (ERC) under the European Union’s Horizon 2020 research and innovation programme
  (grant agreement no. 715571). The research was supported by the Scientific Service
  Units (SSU) of IST Austria through resources provided by the Bioimaging Facility,
  the Life Science Facility, and the Pre-Clinical Facility, namely Sonja Haslinger
  and Michael Schunn for their animal colony management and support. We would also
  like to thank Chakrabarty Lab for sharing the plasmids for AAV2/6 production. Finally,
  we would like to thank the Siegert team members for discussion about the manuscript.
article_processing_charge: Yes
article_type: original
author:
- first_name: Margaret E
  full_name: Maes, Margaret E
  id: 3838F452-F248-11E8-B48F-1D18A9856A87
  last_name: Maes
  orcid: 0000-0001-9642-1085
- first_name: Gabriele M.
  full_name: Wögenstein, Gabriele M.
  last_name: Wögenstein
- first_name: Gloria
  full_name: Colombo, Gloria
  id: 3483CF6C-F248-11E8-B48F-1D18A9856A87
  last_name: Colombo
  orcid: 0000-0001-9434-8902
- first_name: Raquel
  full_name: Casado Polanco, Raquel
  id: 15240fc1-dbcd-11ea-9d1d-ac5a786425fd
  last_name: Casado Polanco
  orcid: 0000-0001-8293-4568
- first_name: Sandra
  full_name: Siegert, Sandra
  id: 36ACD32E-F248-11E8-B48F-1D18A9856A87
  last_name: Siegert
  orcid: 0000-0001-8635-0877
citation:
  ama: Maes ME, Wögenstein GM, Colombo G, Casado Polanco R, Siegert S. Optimizing
    AAV2/6 microglial targeting identified enhanced efficiency in the photoreceptor
    degenerative environment. <i>Molecular Therapy - Methods and Clinical Development</i>.
    2021;23:210-224. doi:<a href="https://doi.org/10.1016/j.omtm.2021.09.006">10.1016/j.omtm.2021.09.006</a>
  apa: Maes, M. E., Wögenstein, G. M., Colombo, G., Casado Polanco, R., &#38; Siegert,
    S. (2021). Optimizing AAV2/6 microglial targeting identified enhanced efficiency
    in the photoreceptor degenerative environment. <i>Molecular Therapy - Methods
    and Clinical Development</i>. Elsevier. <a href="https://doi.org/10.1016/j.omtm.2021.09.006">https://doi.org/10.1016/j.omtm.2021.09.006</a>
  chicago: Maes, Margaret E, Gabriele M. Wögenstein, Gloria Colombo, Raquel Casado
    Polanco, and Sandra Siegert. “Optimizing AAV2/6 Microglial Targeting Identified
    Enhanced Efficiency in the Photoreceptor Degenerative Environment.” <i>Molecular
    Therapy - Methods and Clinical Development</i>. Elsevier, 2021. <a href="https://doi.org/10.1016/j.omtm.2021.09.006">https://doi.org/10.1016/j.omtm.2021.09.006</a>.
  ieee: M. E. Maes, G. M. Wögenstein, G. Colombo, R. Casado Polanco, and S. Siegert,
    “Optimizing AAV2/6 microglial targeting identified enhanced efficiency in the
    photoreceptor degenerative environment,” <i>Molecular Therapy - Methods and Clinical
    Development</i>, vol. 23. Elsevier, pp. 210–224, 2021.
  ista: Maes ME, Wögenstein GM, Colombo G, Casado Polanco R, Siegert S. 2021. Optimizing
    AAV2/6 microglial targeting identified enhanced efficiency in the photoreceptor
    degenerative environment. Molecular Therapy - Methods and Clinical Development.
    23, 210–224.
  mla: Maes, Margaret E., et al. “Optimizing AAV2/6 Microglial Targeting Identified
    Enhanced Efficiency in the Photoreceptor Degenerative Environment.” <i>Molecular
    Therapy - Methods and Clinical Development</i>, vol. 23, Elsevier, 2021, pp. 210–24,
    doi:<a href="https://doi.org/10.1016/j.omtm.2021.09.006">10.1016/j.omtm.2021.09.006</a>.
  short: M.E. Maes, G.M. Wögenstein, G. Colombo, R. Casado Polanco, S. Siegert, Molecular
    Therapy - Methods and Clinical Development 23 (2021) 210–224.
date_created: 2022-01-23T23:01:28Z
date_published: 2021-12-10T00:00:00Z
date_updated: 2023-11-16T13:12:03Z
day: '10'
ddc:
- '570'
department:
- _id: SaSi
- _id: SiHi
doi: 10.1016/j.omtm.2021.09.006
ec_funded: 1
external_id:
  isi:
  - '000748748500019'
file:
- access_level: open_access
  checksum: 77dc540e8011c5475031bdf6ccef20a6
  content_type: application/pdf
  creator: cchlebak
  date_created: 2022-01-24T07:43:09Z
  date_updated: 2022-01-24T07:43:09Z
  file_id: '10657'
  file_name: 2021_MolTherMethodsClinDev_Maes.pdf
  file_size: 4794147
  relation: main_file
  success: 1
file_date_updated: 2022-01-24T07:43:09Z
has_accepted_license: '1'
intvolume: '        23'
isi: 1
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
page: 210-224
project:
- _id: 25D4A630-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '715571'
  name: Microglia action towards neuronal circuit formation and function in health
    and disease
publication: Molecular Therapy - Methods and Clinical Development
publication_identifier:
  eissn:
  - 2329-0501
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Optimizing AAV2/6 microglial targeting identified enhanced efficiency in the
  photoreceptor degenerative environment
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: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 23
year: '2021'
...
---
_id: '6521'
abstract:
- lang: eng
  text: Microglia have emerged as a critical component of neurodegenerative diseases.
    Genetic manipulation of microglia can elucidate their functional impact in disease.
    In neuroscience, recombinant viruses such as lentiviruses and adeno-associated
    viruses (AAVs) have been successfully used to target various cell types in the
    brain, although effective transduction of microglia is rare. In this review, we
    provide a short background of lentiviruses and AAVs, and strategies for designing
    recombinant viral vectors. Then, we will summarize recent literature on successful
    microglial transductions in vitro and in vivo, and discuss the current challenges.
    Finally, we provide guidelines for reporting the efficiency and specificity of
    viral targeting in microglia, which will enable the microglial research community
    to assess and improve methodologies for future studies.
article_number: '134310'
article_processing_charge: No
article_type: original
author:
- first_name: Margaret E
  full_name: Maes, Margaret E
  id: 3838F452-F248-11E8-B48F-1D18A9856A87
  last_name: Maes
  orcid: 0000-0001-9642-1085
- first_name: Gloria
  full_name: Colombo, Gloria
  id: 3483CF6C-F248-11E8-B48F-1D18A9856A87
  last_name: Colombo
  orcid: 0000-0001-9434-8902
- first_name: Rouven
  full_name: Schulz, Rouven
  id: 4C5E7B96-F248-11E8-B48F-1D18A9856A87
  last_name: Schulz
  orcid: 0000-0001-5297-733X
- first_name: Sandra
  full_name: Siegert, Sandra
  id: 36ACD32E-F248-11E8-B48F-1D18A9856A87
  last_name: Siegert
  orcid: 0000-0001-8635-0877
citation:
  ama: 'Maes ME, Colombo G, Schulz R, Siegert S. Targeting microglia with lentivirus
    and AAV: Recent advances and remaining challenges. <i>Neuroscience Letters</i>.
    2019;707. doi:<a href="https://doi.org/10.1016/j.neulet.2019.134310">10.1016/j.neulet.2019.134310</a>'
  apa: 'Maes, M. E., Colombo, G., Schulz, R., &#38; Siegert, S. (2019). Targeting
    microglia with lentivirus and AAV: Recent advances and remaining challenges. <i>Neuroscience
    Letters</i>. Elsevier. <a href="https://doi.org/10.1016/j.neulet.2019.134310">https://doi.org/10.1016/j.neulet.2019.134310</a>'
  chicago: 'Maes, Margaret E, Gloria Colombo, Rouven Schulz, and Sandra Siegert. “Targeting
    Microglia with Lentivirus and AAV: Recent Advances and Remaining Challenges.”
    <i>Neuroscience Letters</i>. Elsevier, 2019. <a href="https://doi.org/10.1016/j.neulet.2019.134310">https://doi.org/10.1016/j.neulet.2019.134310</a>.'
  ieee: 'M. E. Maes, G. Colombo, R. Schulz, and S. Siegert, “Targeting microglia with
    lentivirus and AAV: Recent advances and remaining challenges,” <i>Neuroscience
    Letters</i>, vol. 707. Elsevier, 2019.'
  ista: 'Maes ME, Colombo G, Schulz R, Siegert S. 2019. Targeting microglia with lentivirus
    and AAV: Recent advances and remaining challenges. Neuroscience Letters. 707,
    134310.'
  mla: 'Maes, Margaret E., et al. “Targeting Microglia with Lentivirus and AAV: Recent
    Advances and Remaining Challenges.” <i>Neuroscience Letters</i>, vol. 707, 134310,
    Elsevier, 2019, doi:<a href="https://doi.org/10.1016/j.neulet.2019.134310">10.1016/j.neulet.2019.134310</a>.'
  short: M.E. Maes, G. Colombo, R. Schulz, S. Siegert, Neuroscience Letters 707 (2019).
date_created: 2019-06-05T13:16:24Z
date_published: 2019-08-10T00:00:00Z
date_updated: 2023-08-28T09:30:57Z
day: '10'
ddc:
- '570'
department:
- _id: SaSi
doi: 10.1016/j.neulet.2019.134310
ec_funded: 1
external_id:
  isi:
  - '000486094600037'
  pmid:
  - '31158432'
file:
- access_level: open_access
  checksum: 553c9dbd39727fbed55ee991c51ca4d1
  content_type: application/pdf
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intvolume: '       707'
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month: '08'
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project:
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  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
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  name: Microglia action towards neuronal circuit formation and function in health
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  name: Modulating microglia through G protein-coupled receptor (GPCR) signaling
publication: Neuroscience Letters
publication_identifier:
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publication_status: published
publisher: Elsevier
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title: 'Targeting microglia with lentivirus and AAV: Recent advances and remaining
  challenges'
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type: journal_article
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volume: 707
year: '2019'
...
