Evidence map›Paper›PMID 9736612›Full record

ArticleThe EMBO journal1998

Engagement of T cell receptor triggers its recruitment to low-density detergent-insoluble membrane domains.

C Montixi, C Langlet, A M Bernard, J Thimonier, C Dubois, M A Wurbel, J P Chauvin, M Pierres, H T He

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 142 papers.

0numbers the graph read from it
0cells of the map it votes in
142citing papers in PubMed
23.5field-weighted citation impact, top 1% 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

142 citing papers in PubMed, 620 citations in OpenAlex.

  1. Review
  2. Lipid metabolism in dendritic cell biology.Immunological reviews · 2023
    Review
  3. Article
  4. Article
  5. T cell receptor (TCR) signaling in health and disease.Signal transduction and targeted therapy · 2021
    Review
  6. Article
  7. Article
  8. Article
  9. T-cell targeted pulmonary siRNA delivery for the treatment of asthma.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2020
    Review
  10. Metabolic signaling in T cells.Cell research · 2020
    Review
  11. Review
  12. Microclusters as T Cell Signaling Hubs: Structure, Kinetics, and Regulation.Frontiers in cell and developmental biology · 2020
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

82 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

9 authors at 4 institutions in 1 country.

C MontixiCentre d'Immunologie INSERM-CNRS de Marseille-Luminy, Case 906, Cedex, France.
C Langlet
A M Bernard
J Thimonier
C Dubois
M A Wurbel
J P Chauvin
M Pierres
H T He
Centre National de la Recherche Scientifique · FRCentre d’Immunologie de Marseille-Luminy · FRInserm · FRInstitut de Biologie du Développement Marseille · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T-cell receptors (TCRs) upon binding to peptide-MHC ligands transduce signals in T lymphocytes. Tyrosine phosphorylations in the cytoplasmic domains of the CD3 (gammadeltaepsilon) and zeta subunits of the TCR complex by Src family kinases initiate the signaling cascades via docking and activation of ZAP-70 kinase and other signaling components. We examined the role of the low-density detergent-insoluble membranes (DIMs) in TCR signaling. Using mouse thymocytes as a model, we characterized the structural organization of DIMs in detail. We then demonstrated that TCR engagement triggered an immediate increase in the amount of TCR/CD3 present in DIMs, which directly involves the engaged receptor complexes. TCR/CD3 recruitment is accompanied by the accumulation of a series of prominent tyrosine-phosphorylated substrates and by an increase of the Lck activity in DIMs. Upon TCR stimulation, the DIM-associated receptor complexes are highly enriched in the hyperphosphorylated p23 zeta chains, contain most of the TCR/CD3-associated, phosphorylation-activated ZAP-70 kinases and seem to integrate into higher order, multiple tyrosine-phosphorylated substrate-containing protein complexes. The TCR/CD3 recruitment was found to depend on the activity of Src family kinases. We thus provide the first demonstration of recuitment of TCR/CD3 to DIMs upon receptor stimulation and propose it as a mechanism whereby TCR engagement is coupled to downstream signaling cascades.

Indexed as

AnimalsCell CompartmentationCetomacrogolDetergentsEnzyme InhibitorsGlycosylphosphatidylinositolsG(M1) GangliosideIntracellular MembranesLymphocyte Specific Protein Tyrosine Kinase p56(lck)MicePhosphoproteinsPhosphorylationProtein-Tyrosine KinasesReceptor-CD3 Complex, Antigen, T-CellReceptors, Antigen, T-CellSignal TransductionCetomacrogolDetergentsEnzyme InhibitorsGlycosylphosphatidylinositolsG(M1) GangliosideLymphocyte Specific Protein Tyrosine Kinase p56(lck)PhosphoproteinsProtein-Tyrosine KinasesReceptor-CD3 Complex, Antigen, T-CellReceptors, Antigen, T-Cellsrc-Family KinasesTyrosineZap70 protein, mouseZAP-70 Protein-Tyrosine Kinase

Identifiers

PMID9736612
PMCPMC1170860
OpenAlexW2068504553

What OpenQuestion holds

Textmetadata
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.