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PMID: 8440731 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Multiple components of the T cell antigen receptor complex become tyrosine-phosphorylated upon activation.

The Journal of biological chemistry ·Vol. 268 ·No. 6 ·1993-02-25 ·Pages 4488-93

Qian D, Griswold-Prenner I, Rosner MR, Fitch FW

Abstract

Triggering of the multicomponent T cell antigen receptor (TCR) complex results in several biochemical processes which are critical for the functional activation of T lymphocytes. One common process is the tyrosine phosphorylation of several proteins, including the TCR zeta chain. Here we show that in addition to TCR zeta, other subunits (CD3 gamma, CD3 delta, and CD3 epsilon) of the TCR complex can also be tyrosine-phosphorylated in response to antigen receptor stimulation. This rapid phosphorylation was detected in several mature murine T cell subsets, including CD4+ type 1 and 2 helper cells (TH1 and TH2). Therefore, tyrosine phosphorylation of multiple TCR components in addition to TCR zeta may be an important event during the initiation of the signaling cascade leading to T cell activation.

MeSH Terms
Animals CD3 Complex/metabolism Clone Cells Cricetinae Lymphocyte Activation Mice Phosphorylation Protein-Tyrosine Kinases/metabolism Receptors, Antigen, T-Cell/metabolism T-Lymphocyte Subsets T-Lymphocytes/immunology Tumor Cells, Cultured Tyrosine/metabolism
Chemicals
CD3 Complex Receptors, Antigen, T-Cell Tyrosine Protein-Tyrosine Kinases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Qian D
Department of Pathology, University of Chicago, Illinois 60637.
Griswold-Prenner I
Rosner M R
Fitch F W
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1993-02-25
Pages
4488-93
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NCI NIH HHS · CA35541 · United States
NCI NIH HHS · CA44372 · United States
NIGMS NIH HHS · GM07197 · United States
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