Transmembrane polar residues of TCR beta chain are required for signal transduction
Author(s) -
Sheryl L. Fuller-Espie
Publication year - 1998
Publication title -
international immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.86
H-Index - 134
eISSN - 1460-2377
pISSN - 0953-8178
DOI - 10.1093/intimm/10.7.923
Subject(s) - t cell receptor , transmembrane protein , transmembrane domain , signal transduction , alpha chain , serine , microbiology and biotechnology , cd3 , biology , immunoprecipitation , beta (programming language) , chemistry , mutation , mutant , antigen , cd8 , biochemistry , receptor , t cell , phosphorylation , genetics , immune system , gene , computer science , programming language
Mutagenic analyses have identified structural motifs important for TCR-mediated signaling in the antigen-binding chains, CD3 and zeta subunits of the TCR complex. In this study, we altered selected residues in the transmembrane and extracellular constant regions of the TCR beta chain and expressed the mutants in a T hybridoma line bearing endogenous receptor. We measured cytokine production and apoptosis in response to antigen or antibody. We found that mutation of one or both of the transmembrane tyrosine residues in the TCR beta chain caused a marked reduction in responsiveness. Mutation of the transmembrane serine to alanine also reduced responses, although less markedly. Immunoprecipitation analyses showed that the TCR beta mutations did not alter association with zeta. These experiments identify a signaling role for the transmembrane domain of the TCR beta chain.
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