Regulation of T cell receptor signaling by tyrosine phosphatase SYP association with CTLA-4

被引:442
|
作者
Marengere, LEM
Waterhouse, P
Duncan, GS
Mittrucker, HW
Feng, GS
Mak, TW
机构
[1] UNIV TORONTO, AMGEN INST, ONTARIO CANC INST, DEPT IMMUNOL, TORONTO, ON M5G 2C1, CANADA
[2] UNIV TORONTO, AMGEN INST, ONTARIO CANC INST, DEPT MED BIOPHYS, TORONTO, ON M5G 2C1, CANADA
[3] INDIANA UNIV, SCH MED, DEPT BIOCHEM & MOLEC BIOL, INDIANAPOLIS, IN 46202 USA
[4] INDIANA UNIV, SCH MED, WALTHER ONCOL CTR, INDIANAPOLIS, IN 46202 USA
关键词
D O I
10.1126/science.272.5265.1170
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The absence of CTLA-4 results in uncontrolled T cell proliferation. The T cell receptor-specific kinases FYN, LCK, and ZAP-70 as well as the RAS pathway were found to be activated in T cells of Ctla-4(-/-) mutant mice. In addition, CTLA-4 specifically associated with the tyrosine phosphatase SYP, an interaction mediated by the SRC homology 2 (SH2) domains SYP and phosphotyrosine sequence Tyr-Val-Lys-Met within the CTLA-4 cytoplasmic tail. The CTLA-4-associated SYP had phosphatase activity toward the RAS regulator p52(SHC). Thus, the RAS pathway and T cell activation through the T cell receptor are regulated by CTLA-4-associated SYP.
引用
收藏
页码:1170 / 1173
页数:4
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