T lymphocyte;
T cell receptor down-regulation;
protein tyrosine kinase inhibitor;
D O I:
10.1002/eji.1830270726
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
T cell receptor (TCR) down-regulation is a consequence of specific receptor engagement and plays an important role in modulating the T cell response. We have investigated the role of protein kinase C (PKC) and protein tyrosine kinases (PTK) in the induction of TCR down-regulation. We report that the mutation of S126 in the CD3-gamma chain that is known to inhibit phorbol-12-myristate 13-acetate-induced TCR down-regulation does not affect down-regulation induced by a specific agonist. In addition, agonist-induced TCR down-regulation is not affected by blockade or depletion of PKC, neither by blockade or lack of PTK, while the same treatments efficiently interfere with T cell activation. These results demonstrate that TCR down-regulation is induced by early events which follow specific engagement by an agonist and can be dissociated from those required for full T cell activation.
机构:
UNIV CALIF SAN FRANCISCO, DEPT MICROBIOL & IMMUNOL, HOWARD HUGHES MED INST, SAN FRANCISCO, CA 94143 USAUNIV CALIF SAN FRANCISCO, DEPT MICROBIOL & IMMUNOL, HOWARD HUGHES MED INST, SAN FRANCISCO, CA 94143 USA
WEISS, A
LITTMAN, DR
论文数: 0引用数: 0
h-index: 0
机构:
UNIV CALIF SAN FRANCISCO, DEPT MICROBIOL & IMMUNOL, HOWARD HUGHES MED INST, SAN FRANCISCO, CA 94143 USAUNIV CALIF SAN FRANCISCO, DEPT MICROBIOL & IMMUNOL, HOWARD HUGHES MED INST, SAN FRANCISCO, CA 94143 USA
机构:
UNIV CALIF SAN FRANCISCO, DEPT MICROBIOL & IMMUNOL, HOWARD HUGHES MED INST, SAN FRANCISCO, CA 94143 USAUNIV CALIF SAN FRANCISCO, DEPT MICROBIOL & IMMUNOL, HOWARD HUGHES MED INST, SAN FRANCISCO, CA 94143 USA
WEISS, A
LITTMAN, DR
论文数: 0引用数: 0
h-index: 0
机构:
UNIV CALIF SAN FRANCISCO, DEPT MICROBIOL & IMMUNOL, HOWARD HUGHES MED INST, SAN FRANCISCO, CA 94143 USAUNIV CALIF SAN FRANCISCO, DEPT MICROBIOL & IMMUNOL, HOWARD HUGHES MED INST, SAN FRANCISCO, CA 94143 USA