Evidence map›Paper›PMID 24899501›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

Membrane association of the CD3ε signaling domain is required for optimal T cell development and function.

Matthew L Bettini, Clifford Guy, Pradyot Dash, Kate M Vignali, David E Hamm, Jessica Dobbins, Etienne Gagnon, Paul G Thomas, Kai W Wucherpfennig, Dario A A Vignali

Open access · greenAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. CD3ε of a pan T cell marker involved in mouseInternational journal of ophthalmology · 2024
    Article
  8. Article
  9. Review
  10. Cytotoxic CD8British journal of cancer · 2021
    Review
  11. Structural understanding of T cell receptor triggering.Cellular & molecular immunology · 2020
    Review
  12. Article
  13. Receptor-mediated cell mechanosensing.Molecular biology of the cell · 2017
    Review
  14. Review
  15. Article
  16. Ionic CD3-Lck interaction regulates the initiation of T-cell receptor signaling.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  17. Article
  18. Article
  19. Review
  20. Article
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

10 authors at 3 institutions in 1 country.

Matthew L BettiniDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN, 38105;
Clifford GuyDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN, 38105;
Pradyot DashDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN, 38105;
Kate M VignaliDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN, 38105;
David E HammAdaptive Biotechnologies, Seattle, WA 98102; and.
Jessica DobbinsDepartment of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Boston, MA 02115.
Etienne GagnonDepartment of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Boston, MA 02115.
Paul G ThomasDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN, 38105;
Kai W WucherpfennigDepartment of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Boston, MA 02115.
Dario A A VignaliDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN, 38105; dvignali@pitt.edu.
St. Jude Children's Research Hospital · USDana-Farber Cancer Institute · USAdaptive Biotechnologies (United States) · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
Structural Determinants of TCR Assembly and SignalingR01AI054520 · NIAID · DANA-FARBER CANCER INSTITUTE · PI WUCHERPFENNIG, KAI W · 2003 to 2013
$4.0M
Molecular Control of TCR Signaling and FunctionR01AI052199 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI VIGNALI, DARIO AA · 2003 to 2015
$3.8M
Mechanisms to diversify repertoire and modify T cell activity after infectionR01AI107625 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI THOMAS, PAUL G. · 2013 to 2017
$2.3M
NCI NIH HHS CA21765NCI NIH HHS P30 CA021765NIAID NIH HHS R01 AI052199NIAID NIH HHS R01 AI054520NIAID NIH HHS R01 AI107625NIAID NIH HHS R01 AI52199
6 · The paper itself

Abstract

The TCR:CD3 complex transduces signals that are critical for optimal T cell development and adaptive immunity. In resting T cells, the CD3ε cytoplasmic tail associates with the plasma membrane via a proximal basic-rich stretch (BRS). In this study, we show that mice lacking a functional CD3ε-BRS exhibited substantial reductions in thymic cellularity and limited CD4- CD8- double-negative (DN) 3 to DN4 thymocyte transition, because of enhanced DN4 TCR signaling resulting in increased cell death and TCR downregulation in all subsequent populations. Furthermore, positive, but not negative, T cell selection was affected in mice lacking a functional CD3ε-BRS, which led to limited peripheral T cell function and substantially reduced responsiveness to influenza infection. Collectively, these results indicate that membrane association of the CD3ε signaling domain is required for optimal thymocyte development and peripheral T cell function.

Indexed as

AnimalsCD3 ComplexCell MembraneMiceMice, KnockoutProtein Structure, TertiaryReceptors, Antigen, T-CellSignal TransductionThymocytesCD3 ComplexCd3e protein, mouseReceptors, Antigen, T-Cell

Identifiers

PMID24899501
PMCPMC4065803
OpenAlexW1958617503

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.