Evidence map›Paper›PMID 8433999›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1993

Correlation between Src family member regulation by the protein-tyrosine-phosphatase CD45 and transmembrane signaling through the T-cell receptor.

E D Cahir McFarland, T R Hurley, J T Pingel, B M Sefton, A Shaw, M L Thomas

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
10.1field-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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 198 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Propulsive cell entry diverts pathogens from immune degradation by remodeling the phagocytic synapse.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  7. How the Discovery of the CD4/CD8-p56Frontiers in cell and developmental biology · 2021
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. T-cell receptor signaling is mediated by transient Lck activity, which is inhibited by inorganic mercury.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2009
    Article
  16. Article
  17. Th1 and Th2 cells form morphologically distinct immunological synapses.Journal of immunology (Baltimore, Md. : 1950) · 2008
    Article
  18. Article
  19. Article
  20. Review
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

6 authors at 1 institution in 1 country.

E D Cahir McFarlandDepartment of Pathology, Washington University School of Medicine, St. Louis, MO 63110.
T R Hurley
J T Pingel
B M Sefton
A Shaw
M L Thomas
Washington University in St. Louis · US

Funding

TRAINING PROGRAM IN IMMUNOLOGY AND IMMUNOGENETICST32AI007163 · NIAID · WASHINGTON UNIVERSITY · PI Kenneth M Murphy, Kodi S Ravichandran · 1985 to 2026
$14.8M
THYMOMA TYROSINE PROTEIN KINASER01CA042350 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI SEFTON, BARTHOLOMEW M · 1986 to 2004
$1.9M
LEUKOCYTE SURFACE GLYCOPROTEINS--FUNCTION AND REGULATIONR01AI026363 · NIAID · WASHINGTON UNIVERSITY · PI WOODFORD-THOMAS, TERRY A · 1988 to 1998
–
NCI NIH HHS CA 42350NIAID NIH HHS AI 07163NIAID NIH HHS AI 26363
6 · The paper itself

Abstract

Stimulation of tyrosine phosphorylation is an early and important event in antigen-induced T-cell activation. T-cell clones deficient in expression of CD45, a transmembrane protein-tyrosine-phosphatase (protein-tyrosine-phosphate phosphohydrolase, EC 3.1.3.48), are impaired in their ability to respond to either antigen or T-cell receptor cross-linking. Analysis of the CD45-deficient CD8+ T-cell clone L3M-93 demonstrates that the Src family members p56lck and p59fyn show increased immunoreactivity with anti-phosphotyrosine antibody and exhibit decreased kinase activity. The site of increased tyrosine phosphorylation in Src family members was identified by comparison of cyanogen bromide peptide maps. Phosphorylation of the C-terminal phosphopeptide, containing the negative regulatory site of tyrosine phosphorylation, from the CD45-deficient cells was increased 8-fold for p56lck and 2-fold for p59fyn. These data suggest that CD45 dephosphorylates the negative regulatory site of multiple Src family members in the cytotoxic T-lymphocyte clone L3 and show a correlation between the ability to respond efficiently to antigen and the dephosphorylation of Src family members by CD45.

Indexed as

Genes, srcSignal TransductionAnimalsCell MembraneClone CellsCyanogen BromideImmunoblottingLeukocyte Common AntigensLymphocyte ActivationLymphocyte Specific Protein Tyrosine Kinase p56(lck)Peptide FragmentsPeptide MappingPhosphorylationProtein-Tyrosine KinasesProtein Tyrosine PhosphatasesProto-Oncogene ProteinsCyanogen BromideLeukocyte Common AntigensLymphocyte Specific Protein Tyrosine Kinase p56(lck)Peptide FragmentsProtein-Tyrosine KinasesProtein Tyrosine PhosphatasesProto-Oncogene ProteinsProto-Oncogene Proteins c-fynReceptors, Antigen, T-Cell

Identifiers

PMID8433999
PMCPMC45881
OpenAlexW2163995402

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.