Sequential Interactions of the TCR with Two Distinct Cytoplasmic Tyrosine Kinases

被引:675
作者
Iwashima, Makio
Irving, Bryan A.
van Oers, Nicolai S. C.
Chan, Andrew C.
Weiss, Arthur [1 ]
机构
[1] Univ Calif San Francisco, Dept Med, Howard Hughes Med Inst, San Francisco, CA 94143 USA
关键词
CELL ANTIGEN RECEPTOR; T-CELL; SIGNAL-TRANSDUCTION; ZETA-CHAIN; SH2; DOMAINS; ACTIVATION; CD4; PHOSPHORYLATION; P56LCK; COMPLEX;
D O I
10.1126/science.7509083
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The T cell antigen receptor (TCR) inihates signals by interacting with cytoplasmic protein tyrosine kinases (PTKs) through a 17-residue sequence motif [called the antigen recognition activation motif (ARAM)] that is contained in the TCR zeta and CD3 chains. TCR stimulation induces the tyrosine phosphoryiation of several cellular substrates, including the ARAMs. Lck kinase activity is required for phosphorylation of two conserved tyrosine residues in an ARAM. This phosphorylation leads to the recruitment of a second cytoplasmic PTK, ZAP-70, through both of the ZAP-70 Src homology 2 domains and its phosphorylation. Thus, TCR signal transduction is initiated by the sequential interaction of two PTK.s with TCR ARAMs.
引用
收藏
页码:4279 / 4282
页数:4
相关论文
共 47 条