Evidence map›Paper›PMID 19349987›Full record

ArticleNature immunology2009

T cell antigen receptor signaling and immunological synapse stability require myosin IIA.

Tal Ilani, Gaia Vasiliver-Shamis, Santosh Vardhana, Anthony Bretscher, Michael L Dustin

Open access · greenAbstract read
In one paragraph

Article in Nature immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 129 papers.

0numbers the graph read from it
0cells of the map it votes in
129citing papers in PubMed
9.4field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

129 citing papers in PubMed, 218 citations in OpenAlex.

  1. Trial
  2. Article
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  6. Article
  7. Heterogeneity of Signaling Complex Nanostructure in T Cells Activated Via the T Cell Antigen Receptor.Microscopy and microanalysis : the official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada · 2023
    Article
  8. Review
  9. Joining Forces for Cancer Treatment: From "TCR versus CAR" to "TCR and CAR".International journal of molecular sciences · 2022
    Review
  10. Article
  11. Article
  12. Programmable DNA-augmented hydrogels for controlled activation of human lymphocytes.Nanomedicine : nanotechnology, biology, and medicine · 2021
    Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. The Swing of Lipids at Peroxisomes and Endolysosomes in T Cell Activation.International journal of molecular sciences · 2020
    Review
  18. Review
  19. Article
  20. Article

69 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Tal IlaniDepartment of Molecular Biology and Genetics, Weill Institute for Cell and Molecular Biology, Cornell University, Ithaca, New York, USA.
Gaia Vasiliver-Shamis
Santosh Vardhana
Anthony Bretscher
Michael L Dustin
New York University · USCornell University · US

Funding

Nanomedicine development center for mechanobiologyPN2EY016586 · NEI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DUSTIN, MICHAEL LORAN · 2005 to 2014
$23.0M
MICROFILAMENT ORGANIZATION AND REGULATIONR01GM036652 · NIGMS · CORNELL UNIVERSITY ITHACA · PI BRETSCHER, ANTHONY P. · 1986 to 2018
$8.7M
PHYSIOLOGICAL CHEMISTRY OF INTEGRIN FUNCTIONR01AI044931 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DUSTIN, MICHAEL LORAN · 1999 to 2007
$1.5M
Physiological Chemistry of Integrin FunctionR56AI044931 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DUSTIN, MICHAEL LORAN · 2009 to 2010
$474k
Center for Mechanotransduction and Nanomedicine. (RMI)PN1EY016586 · NEI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI SHEETZ, MICHAEL PATRICK · 2004 to 2004
$81k
NEI NIH HHS EY16586NEI NIH HHS PN1 EY016586NEI NIH HHS PN2 EY016586NIAID NIH HHS AI44931NIAID NIH HHS R01 AI044931NIAID NIH HHS R56 AI044931NIGMS NIH HHS GM36652NIGMS NIH HHS R01 GM036652
6 · The paper itself

Abstract

Immunological synapses are initiated by signaling in discrete T cell antigen receptor microclusters and are important for the differentiation and effector functions of T cells. Synapse formation involves the orchestrated movement of microclusters toward the center of the contact area with the antigen-presenting cell. Microcluster movement is associated with centripetal actin flow, but the function of motor proteins is unknown. Here we show that myosin IIA was necessary for complete assembly and movement of T cell antigen receptor microclusters. In the absence of myosin IIA or its ATPase activity, T cell signaling was interrupted 'downstream' of the kinase Lck and the synapse was destabilized. Thus, T cell antigen receptor signaling and the subsequent formation of immunological synapses are active processes dependent on myosin IIA.

Indexed as

Cell DifferentiationFluorescent Antibody TechniqueHumansImmunoblottingImmunological SynapsesJurkat CellsLymphocyte ActivationNonmuscle Myosin Type IIAReceptors, Antigen, T-CellSignal TransductionNonmuscle Myosin Type IIAReceptors, Antigen, T-Cell

Identifiers

PMID19349987
PMCPMC2719775
OpenAlexW2014118715

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.