---
_id: '7875'
abstract:
- lang: eng
  text: 'Cells navigating through complex tissues face a fundamental challenge: while
    multiple protrusions explore different paths, the cell needs to avoid entanglement.
    How a cell surveys and then corrects its own shape is poorly understood. Here,
    we demonstrate that spatially distinct microtubule dynamics regulate amoeboid
    cell migration by locally promoting the retraction of protrusions. In migrating
    dendritic cells, local microtubule depolymerization within protrusions remote
    from the microtubule organizing center triggers actomyosin contractility controlled
    by RhoA and its exchange factor Lfc. Depletion of Lfc leads to aberrant myosin
    localization, thereby causing two effects that rate-limit locomotion: (1) impaired
    cell edge coordination during path finding and (2) defective adhesion resolution.
    Compromised shape control is particularly hindering in geometrically complex microenvironments,
    where it leads to entanglement and ultimately fragmentation of the cell body.
    We thus demonstrate that microtubules can act as a proprioceptive device: they
    sense cell shape and control actomyosin retraction to sustain cellular coherence.'
acknowledged_ssus:
- _id: LifeSc
- _id: Bio
- _id: PreCl
acknowledgement: "The authors thank the Scientific Service Units (Life Sciences, Bioimaging,
  Preclinical) of the Institute of Science and Technology Austria for excellent support.
  This work was funded by the European Research Council (ERC StG 281556 and CoG 724373),
  two grants from the Austrian\r\nScience Fund (FWF; P29911 and DK Nanocell W1250-B20
  to M. Sixt) and by the German Research Foundation (DFG SFB1032 project B09) to O.
  Thorn-Seshold and D. Trauner. J. Renkawitz was supported by ISTFELLOW funding from
  the People Program (Marie Curie Actions) of the European Union’s Seventh Framework
  Programme (FP7/2007-2013) under the Research Executive Agency grant agreement (291734)
  and a European Molecular Biology Organization long-term fellowship (ALTF 1396-2014)
  co-funded by the European Commission (LTFCOFUND2013, GA-2013-609409), E. Kiermaier
  by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under Germany’s
  Excellence Strategy—EXC 2151—390873048, and H. Hacker by the American Lebanese Syrian
  Associated ¨Charities. K.-D. Fischer was supported by the Analysis, Imaging and
  Modelling of Neuronal and Inflammatory Processes graduate school funded by the Ministry
  of Economics, Science, and Digitisation of the State Saxony-Anhalt and by the European
  Funds for Social and Regional Development."
article_number: e201907154
article_processing_charge: No
article_type: original
author:
- first_name: Aglaja
  full_name: Kopf, Aglaja
  id: 31DAC7B6-F248-11E8-B48F-1D18A9856A87
  last_name: Kopf
  orcid: 0000-0002-2187-6656
- first_name: Jörg
  full_name: Renkawitz, Jörg
  id: 3F0587C8-F248-11E8-B48F-1D18A9856A87
  last_name: Renkawitz
  orcid: 0000-0003-2856-3369
- first_name: Robert
  full_name: Hauschild, Robert
  id: 4E01D6B4-F248-11E8-B48F-1D18A9856A87
  last_name: Hauschild
  orcid: 0000-0001-9843-3522
- first_name: Irute
  full_name: Girkontaite, Irute
  last_name: Girkontaite
- first_name: Kerry
  full_name: Tedford, Kerry
  last_name: Tedford
- first_name: Jack
  full_name: Merrin, Jack
  id: 4515C308-F248-11E8-B48F-1D18A9856A87
  last_name: Merrin
  orcid: 0000-0001-5145-4609
- first_name: Oliver
  full_name: Thorn-Seshold, Oliver
  last_name: Thorn-Seshold
- first_name: Dirk
  full_name: Trauner, Dirk
  id: E8F27F48-3EBA-11E9-92A1-B709E6697425
  last_name: Trauner
- first_name: Hans
  full_name: Häcker, Hans
  last_name: Häcker
- first_name: Klaus Dieter
  full_name: Fischer, Klaus Dieter
  last_name: Fischer
- first_name: Eva
  full_name: Kiermaier, Eva
  id: 3EB04B78-F248-11E8-B48F-1D18A9856A87
  last_name: Kiermaier
  orcid: 0000-0001-6165-5738
- first_name: Michael K
  full_name: Sixt, Michael K
  id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
  last_name: Sixt
  orcid: 0000-0002-6620-9179
citation:
  ama: Kopf A, Renkawitz J, Hauschild R, et al. Microtubules control cellular shape
    and coherence in amoeboid migrating cells. <i>The Journal of Cell Biology</i>.
    2020;219(6). doi:<a href="https://doi.org/10.1083/jcb.201907154">10.1083/jcb.201907154</a>
  apa: Kopf, A., Renkawitz, J., Hauschild, R., Girkontaite, I., Tedford, K., Merrin,
    J., … Sixt, M. K. (2020). Microtubules control cellular shape and coherence in
    amoeboid migrating cells. <i>The Journal of Cell Biology</i>. Rockefeller University
    Press. <a href="https://doi.org/10.1083/jcb.201907154">https://doi.org/10.1083/jcb.201907154</a>
  chicago: Kopf, Aglaja, Jörg Renkawitz, Robert Hauschild, Irute Girkontaite, Kerry
    Tedford, Jack Merrin, Oliver Thorn-Seshold, et al. “Microtubules Control Cellular
    Shape and Coherence in Amoeboid Migrating Cells.” <i>The Journal of Cell Biology</i>.
    Rockefeller University Press, 2020. <a href="https://doi.org/10.1083/jcb.201907154">https://doi.org/10.1083/jcb.201907154</a>.
  ieee: A. Kopf <i>et al.</i>, “Microtubules control cellular shape and coherence
    in amoeboid migrating cells,” <i>The Journal of Cell Biology</i>, vol. 219, no.
    6. Rockefeller University Press, 2020.
  ista: Kopf A, Renkawitz J, Hauschild R, Girkontaite I, Tedford K, Merrin J, Thorn-Seshold
    O, Trauner D, Häcker H, Fischer KD, Kiermaier E, Sixt MK. 2020. Microtubules control
    cellular shape and coherence in amoeboid migrating cells. The Journal of Cell
    Biology. 219(6), e201907154.
  mla: Kopf, Aglaja, et al. “Microtubules Control Cellular Shape and Coherence in
    Amoeboid Migrating Cells.” <i>The Journal of Cell Biology</i>, vol. 219, no. 6,
    e201907154, Rockefeller University Press, 2020, doi:<a href="https://doi.org/10.1083/jcb.201907154">10.1083/jcb.201907154</a>.
  short: A. Kopf, J. Renkawitz, R. Hauschild, I. Girkontaite, K. Tedford, J. Merrin,
    O. Thorn-Seshold, D. Trauner, H. Häcker, K.D. Fischer, E. Kiermaier, M.K. Sixt,
    The Journal of Cell Biology 219 (2020).
date_created: 2020-05-24T22:00:56Z
date_published: 2020-06-01T00:00:00Z
date_updated: 2023-08-21T06:28:17Z
day: '01'
ddc:
- '570'
department:
- _id: MiSi
- _id: Bio
- _id: NanoFab
doi: 10.1083/jcb.201907154
ec_funded: 1
external_id:
  isi:
  - '000538141100020'
  pmid:
  - '32379884'
file:
- access_level: open_access
  checksum: cb0b9c77842ae1214caade7b77e4d82d
  content_type: application/pdf
  creator: dernst
  date_created: 2020-11-24T13:25:13Z
  date_updated: 2020-11-24T13:25:13Z
  file_id: '8801'
  file_name: 2020_JCellBiol_Kopf.pdf
  file_size: 7536712
  relation: main_file
  success: 1
file_date_updated: 2020-11-24T13:25:13Z
has_accepted_license: '1'
intvolume: '       219'
isi: 1
issue: '6'
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 25A603A2-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '281556'
  name: Cytoskeletal force generation and force transduction of migrating leukocytes
- _id: 25FE9508-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '724373'
  name: Cellular navigation along spatial gradients
- _id: 26018E70-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P29911
  name: Mechanical adaptation of lamellipodial actin
- _id: 252C3B08-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: W 1250-B20
  name: Nano-Analytics of Cellular Systems
- _id: 25681D80-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '291734'
  name: International IST Postdoc Fellowship Programme
- _id: 25A48D24-B435-11E9-9278-68D0E5697425
  grant_number: ALTF 1396-2014
  name: Molecular and system level view of immune cell migration
publication: The Journal of Cell Biology
publication_identifier:
  eissn:
  - 1540-8140
publication_status: published
publisher: Rockefeller University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Microtubules control cellular shape and coherence in amoeboid migrating cells
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: 219
year: '2020'
...
---
_id: '1599'
abstract:
- lang: eng
  text: "The addition of polysialic acid to N- and/or O-linked glycans, referred to
    as polysialylation, is a rare posttranslational modification that is mainly known
    to control the developmental plasticity of the nervous system. Here we show that
    CCR7, the central chemokine receptor controlling immune cell trafficking to secondary
    lymphatic organs, carries polysialic acid. This modification is essential for
    the recognition of the CCR7 ligand CCL21. As a consequence, dendritic cell trafficking
    is abrogated in polysialyltransferase-deficient mice, manifesting as disturbed
    lymph node homeostasis and unresponsiveness to inflammatory stimuli. Structure-function
    analysis of chemokine-receptor interactions reveals that CCL21 adopts an autoinhibited
    conformation, which is released upon interaction with polysialic acid. Thus, we
    describe a glycosylation-mediated immune cell trafficking disorder and its mechanistic
    basis.\r\n"
acknowledged_ssus:
- _id: SSU
acknowledgement: 'We thank S. Schüchner and E. Ogris for kindly providing the antibody
  to GFP, M. Helmbrecht and A. Huber for providing Nrp2−/− mice, the IST Scientific
  Support Facilities for excellent services, and J. Renkawitz and K. Vaahtomeri for
  critically reading the manuscript. '
article_processing_charge: No
article_type: original
author:
- first_name: Eva
  full_name: Kiermaier, Eva
  id: 3EB04B78-F248-11E8-B48F-1D18A9856A87
  last_name: Kiermaier
  orcid: 0000-0001-6165-5738
- first_name: Christine
  full_name: Moussion, Christine
  id: 3356F664-F248-11E8-B48F-1D18A9856A87
  last_name: Moussion
- first_name: Christopher
  full_name: Veldkamp, Christopher
  last_name: Veldkamp
- first_name: Rita
  full_name: Gerardy  Schahn, Rita
  last_name: Gerardy  Schahn
- first_name: Ingrid
  full_name: De Vries, Ingrid
  id: 4C7D837E-F248-11E8-B48F-1D18A9856A87
  last_name: De Vries
- first_name: Larry
  full_name: Williams, Larry
  last_name: Williams
- first_name: Gary
  full_name: Chaffee, Gary
  last_name: Chaffee
- first_name: Andrew
  full_name: Phillips, Andrew
  last_name: Phillips
- first_name: Friedrich
  full_name: Freiberger, Friedrich
  last_name: Freiberger
- first_name: Richard
  full_name: Imre, Richard
  last_name: Imre
- first_name: Deni
  full_name: Taleski, Deni
  last_name: Taleski
- first_name: Richard
  full_name: Payne, Richard
  last_name: Payne
- first_name: Asolina
  full_name: Braun, Asolina
  last_name: Braun
- first_name: Reinhold
  full_name: Förster, Reinhold
  last_name: Förster
- first_name: Karl
  full_name: Mechtler, Karl
  last_name: Mechtler
- first_name: Martina
  full_name: Mühlenhoff, Martina
  last_name: Mühlenhoff
- first_name: Brian
  full_name: Volkman, Brian
  last_name: Volkman
- first_name: Michael K
  full_name: Sixt, Michael K
  id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
  last_name: Sixt
  orcid: 0000-0002-6620-9179
citation:
  ama: Kiermaier E, Moussion C, Veldkamp C, et al. Polysialylation controls dendritic
    cell trafficking by regulating chemokine recognition. <i>Science</i>. 2016;351(6269):186-190.
    doi:<a href="https://doi.org/10.1126/science.aad0512">10.1126/science.aad0512</a>
  apa: Kiermaier, E., Moussion, C., Veldkamp, C., Gerardy  Schahn, R., de Vries, I.,
    Williams, L., … Sixt, M. K. (2016). Polysialylation controls dendritic cell trafficking
    by regulating chemokine recognition. <i>Science</i>. American Association for
    the Advancement of Science. <a href="https://doi.org/10.1126/science.aad0512">https://doi.org/10.1126/science.aad0512</a>
  chicago: Kiermaier, Eva, Christine Moussion, Christopher Veldkamp, Rita Gerardy 
    Schahn, Ingrid de Vries, Larry Williams, Gary Chaffee, et al. “Polysialylation
    Controls Dendritic Cell Trafficking by Regulating Chemokine Recognition.” <i>Science</i>.
    American Association for the Advancement of Science, 2016. <a href="https://doi.org/10.1126/science.aad0512">https://doi.org/10.1126/science.aad0512</a>.
  ieee: E. Kiermaier <i>et al.</i>, “Polysialylation controls dendritic cell trafficking
    by regulating chemokine recognition,” <i>Science</i>, vol. 351, no. 6269. American
    Association for the Advancement of Science, pp. 186–190, 2016.
  ista: Kiermaier E, Moussion C, Veldkamp C, Gerardy  Schahn R, de Vries I, Williams
    L, Chaffee G, Phillips A, Freiberger F, Imre R, Taleski D, Payne R, Braun A, Förster
    R, Mechtler K, Mühlenhoff M, Volkman B, Sixt MK. 2016. Polysialylation controls
    dendritic cell trafficking by regulating chemokine recognition. Science. 351(6269),
    186–190.
  mla: Kiermaier, Eva, et al. “Polysialylation Controls Dendritic Cell Trafficking
    by Regulating Chemokine Recognition.” <i>Science</i>, vol. 351, no. 6269, American
    Association for the Advancement of Science, 2016, pp. 186–90, doi:<a href="https://doi.org/10.1126/science.aad0512">10.1126/science.aad0512</a>.
  short: E. Kiermaier, C. Moussion, C. Veldkamp, R. Gerardy  Schahn, I. de Vries,
    L. Williams, G. Chaffee, A. Phillips, F. Freiberger, R. Imre, D. Taleski, R. Payne,
    A. Braun, R. Förster, K. Mechtler, M. Mühlenhoff, B. Volkman, M.K. Sixt, Science
    351 (2016) 186–190.
date_created: 2018-12-11T11:52:57Z
date_published: 2016-01-08T00:00:00Z
date_updated: 2021-01-12T06:51:52Z
day: '08'
department:
- _id: MiSi
doi: 10.1126/science.aad0512
ec_funded: 1
external_id:
  pmid:
  - '26657283'
intvolume: '       351'
issue: '6269'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5583642/
month: '01'
oa: 1
oa_version: Submitted Version
page: 186 - 190
pmid: 1
project:
- _id: 25A603A2-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '281556'
  name: Cytoskeletal force generation and force transduction of migrating leukocytes
    (EU)
- _id: 25A76F58-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '289720'
  name: Stromal Cell-immune Cell Interactions in Health and Disease
- _id: 25A8E5EA-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: Y 564-B12
  name: Cytoskeletal force generation and transduction of leukocytes (FWF)
publication: Science
publication_status: published
publisher: American Association for the Advancement of Science
publist_id: '5570'
quality_controlled: '1'
scopus_import: 1
status: public
title: Polysialylation controls dendritic cell trafficking by regulating chemokine
  recognition
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 351
year: '2016'
...
---
_id: '1618'
abstract:
- lang: eng
  text: CCL19 and CCL21 are chemokines involved in the trafficking of immune cells,
    particularly within the lymphatic system, through activation of CCR7. Concurrent
    expression of PSGL-1 and CCR7 in naive T-cells enhances recruitment of these cells
    to secondary lymphoid organs by CCL19 and CCL21. Here the solution structure of
    CCL19 is reported. It contains a canonical chemokine domain. Chemical shift mapping
    shows the N-termini of PSGL-1 and CCR7 have overlapping binding sites for CCL19
    and binding is competitive. Implications for the mechanism of PSGL-1's enhancement
    of resting T-cell recruitment are discussed.
article_processing_charge: No
author:
- first_name: Christopher
  full_name: Veldkamp, Christopher
  last_name: Veldkamp
- first_name: Eva
  full_name: Kiermaier, Eva
  id: 3EB04B78-F248-11E8-B48F-1D18A9856A87
  last_name: Kiermaier
  orcid: 0000-0001-6165-5738
- first_name: Skylar
  full_name: Gabel Eissens, Skylar
  last_name: Gabel Eissens
- first_name: Miranda
  full_name: Gillitzer, Miranda
  last_name: Gillitzer
- first_name: David
  full_name: Lippner, David
  last_name: Lippner
- first_name: Frank
  full_name: Disilvio, Frank
  last_name: Disilvio
- first_name: Casey
  full_name: Mueller, Casey
  last_name: Mueller
- first_name: Paeton
  full_name: Wantuch, Paeton
  last_name: Wantuch
- first_name: Gary
  full_name: Chaffee, Gary
  last_name: Chaffee
- first_name: Michael
  full_name: Famiglietti, Michael
  last_name: Famiglietti
- first_name: Danielle
  full_name: Zgoba, Danielle
  last_name: Zgoba
- first_name: Asha
  full_name: Bailey, Asha
  last_name: Bailey
- first_name: Yaya
  full_name: Bah, Yaya
  last_name: Bah
- first_name: Samantha
  full_name: Engebretson, Samantha
  last_name: Engebretson
- first_name: David
  full_name: Graupner, David
  last_name: Graupner
- first_name: Emily
  full_name: Lackner, Emily
  last_name: Lackner
- first_name: Vincent
  full_name: Larosa, Vincent
  last_name: Larosa
- first_name: Tysha
  full_name: Medeiros, Tysha
  last_name: Medeiros
- first_name: Michael
  full_name: Olson, Michael
  last_name: Olson
- first_name: Andrew
  full_name: Phillips, Andrew
  last_name: Phillips
- first_name: Harley
  full_name: Pyles, Harley
  last_name: Pyles
- first_name: Amanda
  full_name: Richard, Amanda
  last_name: Richard
- first_name: Scott
  full_name: Schoeller, Scott
  last_name: Schoeller
- first_name: Boris
  full_name: Touzeau, Boris
  last_name: Touzeau
- first_name: Larry
  full_name: Williams, Larry
  last_name: Williams
- first_name: Michael K
  full_name: Sixt, Michael K
  id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
  last_name: Sixt
  orcid: 0000-0002-6620-9179
- first_name: Francis
  full_name: Peterson, Francis
  last_name: Peterson
citation:
  ama: Veldkamp C, Kiermaier E, Gabel Eissens S, et al. Solution structure of CCL19
    and identification of overlapping CCR7 and PSGL-1 binding sites. <i>Biochemistry</i>.
    2015;54(27):4163-4166. doi:<a href="https://doi.org/10.1021/acs.biochem.5b00560">10.1021/acs.biochem.5b00560</a>
  apa: Veldkamp, C., Kiermaier, E., Gabel Eissens, S., Gillitzer, M., Lippner, D.,
    Disilvio, F., … Peterson, F. (2015). Solution structure of CCL19 and identification
    of overlapping CCR7 and PSGL-1 binding sites. <i>Biochemistry</i>. American Chemical
    Society. <a href="https://doi.org/10.1021/acs.biochem.5b00560">https://doi.org/10.1021/acs.biochem.5b00560</a>
  chicago: Veldkamp, Christopher, Eva Kiermaier, Skylar Gabel Eissens, Miranda Gillitzer,
    David Lippner, Frank Disilvio, Casey Mueller, et al. “Solution Structure of CCL19
    and Identification of Overlapping CCR7 and PSGL-1 Binding Sites.” <i>Biochemistry</i>.
    American Chemical Society, 2015. <a href="https://doi.org/10.1021/acs.biochem.5b00560">https://doi.org/10.1021/acs.biochem.5b00560</a>.
  ieee: C. Veldkamp <i>et al.</i>, “Solution structure of CCL19 and identification
    of overlapping CCR7 and PSGL-1 binding sites,” <i>Biochemistry</i>, vol. 54, no.
    27. American Chemical Society, pp. 4163–4166, 2015.
  ista: Veldkamp C, Kiermaier E, Gabel Eissens S, Gillitzer M, Lippner D, Disilvio
    F, Mueller C, Wantuch P, Chaffee G, Famiglietti M, Zgoba D, Bailey A, Bah Y, Engebretson
    S, Graupner D, Lackner E, Larosa V, Medeiros T, Olson M, Phillips A, Pyles H,
    Richard A, Schoeller S, Touzeau B, Williams L, Sixt MK, Peterson F. 2015. Solution
    structure of CCL19 and identification of overlapping CCR7 and PSGL-1 binding sites.
    Biochemistry. 54(27), 4163–4166.
  mla: Veldkamp, Christopher, et al. “Solution Structure of CCL19 and Identification
    of Overlapping CCR7 and PSGL-1 Binding Sites.” <i>Biochemistry</i>, vol. 54, no.
    27, American Chemical Society, 2015, pp. 4163–66, doi:<a href="https://doi.org/10.1021/acs.biochem.5b00560">10.1021/acs.biochem.5b00560</a>.
  short: C. Veldkamp, E. Kiermaier, S. Gabel Eissens, M. Gillitzer, D. Lippner, F.
    Disilvio, C. Mueller, P. Wantuch, G. Chaffee, M. Famiglietti, D. Zgoba, A. Bailey,
    Y. Bah, S. Engebretson, D. Graupner, E. Lackner, V. Larosa, T. Medeiros, M. Olson,
    A. Phillips, H. Pyles, A. Richard, S. Schoeller, B. Touzeau, L. Williams, M.K.
    Sixt, F. Peterson, Biochemistry 54 (2015) 4163–4166.
date_created: 2018-12-11T11:53:03Z
date_published: 2015-06-26T00:00:00Z
date_updated: 2023-03-30T11:32:57Z
day: '26'
department:
- _id: MiSi
doi: 10.1021/acs.biochem.5b00560
ec_funded: 1
external_id:
  pmid:
  - '26115234'
intvolume: '        54'
issue: '27'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4809050/
month: '06'
oa: 1
oa_version: Submitted Version
page: 4163 - 4166
pmid: 1
project:
- _id: 25A603A2-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '281556'
  name: Cytoskeletal force generation and force transduction of migrating leukocytes
    (EU)
publication: Biochemistry
publication_status: published
publisher: American Chemical Society
publist_id: '5548'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Solution structure of CCL19 and identification of overlapping CCR7 and PSGL-1
  binding sites
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 54
year: '2015'
...
---
_id: '1686'
author:
- first_name: Eva
  full_name: Kiermaier, Eva
  id: 3EB04B78-F248-11E8-B48F-1D18A9856A87
  last_name: Kiermaier
  orcid: 0000-0001-6165-5738
- first_name: Michael K
  full_name: Sixt, Michael K
  id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
  last_name: Sixt
  orcid: 0000-0002-6620-9179
citation:
  ama: 'Kiermaier E, Sixt MK. Fragmented communication between immune cells: Neutrophils
    blaze a trail with migratory cues for T cells to follow to sites of infection.
    <i>Science</i>. 2015;349(6252):1055-1056. doi:<a href="https://doi.org/10.1126/science.aad0867">10.1126/science.aad0867</a>'
  apa: 'Kiermaier, E., &#38; Sixt, M. K. (2015). Fragmented communication between
    immune cells: Neutrophils blaze a trail with migratory cues for T cells to follow
    to sites of infection. <i>Science</i>. American Association for the Advancement
    of Science. <a href="https://doi.org/10.1126/science.aad0867">https://doi.org/10.1126/science.aad0867</a>'
  chicago: 'Kiermaier, Eva, and Michael K Sixt. “Fragmented Communication between
    Immune Cells: Neutrophils Blaze a Trail with Migratory Cues for T Cells to Follow
    to Sites of Infection.” <i>Science</i>. American Association for the Advancement
    of Science, 2015. <a href="https://doi.org/10.1126/science.aad0867">https://doi.org/10.1126/science.aad0867</a>.'
  ieee: 'E. Kiermaier and M. K. Sixt, “Fragmented communication between immune cells:
    Neutrophils blaze a trail with migratory cues for T cells to follow to sites of
    infection,” <i>Science</i>, vol. 349, no. 6252. American Association for the Advancement
    of Science, pp. 1055–1056, 2015.'
  ista: 'Kiermaier E, Sixt MK. 2015. Fragmented communication between immune cells:
    Neutrophils blaze a trail with migratory cues for T cells to follow to sites of
    infection. Science. 349(6252), 1055–1056.'
  mla: 'Kiermaier, Eva, and Michael K. Sixt. “Fragmented Communication between Immune
    Cells: Neutrophils Blaze a Trail with Migratory Cues for T Cells to Follow to
    Sites of Infection.” <i>Science</i>, vol. 349, no. 6252, American Association
    for the Advancement of Science, 2015, pp. 1055–56, doi:<a href="https://doi.org/10.1126/science.aad0867">10.1126/science.aad0867</a>.'
  short: E. Kiermaier, M.K. Sixt, Science 349 (2015) 1055–1056.
date_created: 2018-12-11T11:53:28Z
date_published: 2015-09-04T00:00:00Z
date_updated: 2021-01-12T06:52:31Z
day: '04'
department:
- _id: MiSi
doi: 10.1126/science.aad0867
intvolume: '       349'
issue: '6252'
language:
- iso: eng
month: '09'
oa_version: None
page: 1055 - 1056
publication: Science
publication_status: published
publisher: American Association for the Advancement of Science
publist_id: '5459'
quality_controlled: '1'
scopus_import: 1
status: public
title: 'Fragmented communication between immune cells: Neutrophils blaze a trail with
  migratory cues for T cells to follow to sites of infection'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 349
year: '2015'
...
