| Literature DB >> 8638161 |
L E Marengère1, P Waterhouse, G S Duncan, H W Mittrücker, G S Feng, T W Mak.
Abstract
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 of SYP and the phosphotyrosine sequence Tyr-Val-Lys-Met within the CTLA-4 cytoplasmic tail. The CTLA-4-associated SYP had phosphatase activity toward the RAS regulator p52SHC. Thus, the RAS pathway and T cell activation through the T cell receptor are regulated by CTLA-4-associated SYP.Entities:
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Year: 1996 PMID: 8638161 DOI: 10.1126/science.272.5265.1170
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728