Evidence map›Paper›PMID 30893608›Full record

ArticleCell reports2019

Cytoskeletal Control of Antigen-Dependent T Cell Activation.

Huw Colin-York, Yousef Javanmardi, Mark Skamrahl, Sudha Kumari, Veronica T Chang, Satya Khuon, Aaron Taylor, Teng-Leong Chew, Eric Betzig, Emad Moeendarbary and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

63 citing papers in PubMed, 90 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
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  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Mechanical force matters in early T cell activation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Measurement of Forces Acting on Single T-Cell Receptors.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  18. Article
  19. DNA Nanotechnology for Investigating Mechanical Signaling in the Immune System.Angewandte Chemie (International ed. in English) · 2023
    Review
  20. Article

3 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

13 authors at 5 institutions in 2 countries.

Huw Colin-YorkMRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Headley Way, Oxford OX3 9DS, UK.
Yousef JavanmardiDepartment of Mechanical Engineering, University College London, London WC1E 7JE, UK.
Mark SkamrahlMRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Headley Way, Oxford OX3 9DS, UK.
Sudha KumariKoch Institute of Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Veronica T ChangMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge Biomedical Campus, Cambridge CB2 0QH, UK.
Satya KhuonJanelia Research Campus, Howard Hughes Medical Institute, 19700 Helix Drive, Ashburn, VA 20147, USA.
Aaron TaylorJanelia Research Campus, Howard Hughes Medical Institute, 19700 Helix Drive, Ashburn, VA 20147, USA.
Teng-Leong ChewJanelia Research Campus, Howard Hughes Medical Institute, 19700 Helix Drive, Ashburn, VA 20147, USA.
Eric BetzigJanelia Research Campus, Howard Hughes Medical Institute, 19700 Helix Drive, Ashburn, VA 20147, USA.
Emad MoeendarbaryDepartment of Mechanical Engineering, University College London, London WC1E 7JE, UK; Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Vincenzo CerundoloMRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Headley Way, Oxford OX3 9DS, UK.
Christian EggelingMRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Headley Way, Oxford OX3 9DS, UK.
Marco FritzscheMRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Headley Way, Oxford OX3 9DS, UK; Kennedy Institute for Rheumatology, University of Oxford, Roosevelt Drive, Oxford OX3 7LF, UK. Electronic address: marco.fritzsche@rdm.ox.ac.uk.
University of Oxford · GBHoward Hughes Medical Institute · USUniversity College London · GBMassachusetts Institute of Technology · USMRC Laboratory of Molecular Biology · GB

Funding

Biotechnology and Biological Sciences Research CouncilCancer Research UK 11331Cancer Research UK 17722Cancer Research UK 22057Cancer Research UK C57744/A22057Howard Hughes Medical InstituteMedical Research Council G0501975Medical Research Council G0800158Medical Research Council G1000800Medical Research Council MC_PC_15002Medical Research Council MC_PC_15060Medical Research Council MC_PC_16082Medical Research Council MC_U137884181Medical Research Council MC_UP_1201/15Medical Research Council MC_UU_00008/1Medical Research Council MC_UU_00008/9Medical Research Council MC_UU_12010/1Medical Research Council MC_UU_12010/9Medical Research Council MR/K01577X/1Wellcome TrustWellcome Trust 091911Wellcome Trust 107457Wellcome Trust 212343/Z/18/Z
6 · The paper itself

Abstract

Cytoskeletal actin dynamics is essential for T cell activation. Here, we show evidence that the binding kinetics of the antigen engaging the T cell receptor influences the nanoscale actin organization and mechanics of the immune synapse. Using an engineered T cell system expressing a specific T cell receptor and stimulated by a range of antigens, we found that the peak force experienced by the T cell receptor during activation was independent of the unbinding kinetics of the stimulating antigen. Conversely, quantification of the actin retrograde flow velocity at the synapse revealed a striking dependence on the antigen unbinding kinetics. These findings suggest that the dynamics of the actin cytoskeleton actively adjusted to normalize the force experienced by the T cell receptor in an antigen-specific manner. Consequently, tuning actin dynamics in response to antigen kinetics may thus be a mechanism that allows T cells to adjust the lengthscale and timescale of T cell receptor signaling.

Indexed as

Lymphocyte ActivationActin CytoskeletonHumansJurkat CellsReceptors, Antigen, T-CellSignal TransductionT-LymphocytesReceptors, Antigen, T-Cellactin dynamicsimmunological synapsemechanosensationmechanosensitivityT cell activationTCR clusterTFM

Identifiers

PMID30893608
PMCPMC6426652
OpenAlexW2925167385

What OpenQuestion holds

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LicenceCC BY
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.