SHP-1 and SHP-2 in T cells: two phosphatases functioning at many levels

被引:280
作者
Lorenz, Ulrike [1 ,2 ]
机构
[1] Univ Virginia, Dept Microbiol, Charlottesville, VA 22908 USA
[2] Univ Virginia, Beirne Carter Ctr Immunol Res, Charlottesville, VA USA
基金
美国国家卫生研究院;
关键词
SHP-1; SHP-2; T cells; motheaten mice; T-cell signaling; T-cell development; PROTEIN-TYROSINE-PHOSPHATASE; IG-LIKE RECEPTOR-1; SRC HOMOLOGY-2 DOMAINS; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; TCR SIGNALING THRESHOLDS; HUMAN PERIPHERAL-BLOOD; MOTH-EATEN MICE; ANTIGEN-RECEPTOR; SH2; DOMAINS; LIPID RAFTS;
D O I
10.1111/j.1600-065X.2008.00760.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tyrosine phosphorylation and dephosphorylation of proteins play a critical role for many T-cell functions. The opposing actions of protein tyrosine kinases (PTKs) and protein tyrosine phosphatases (PTPs) determine the level of tyrosine phosphorylation at any time. It is well accepted that PTKs are essential during T-cell signaling; however, the role and importance of PTPs are much less known and appreciated. Both transmembrane and cytoplasmic tyrosine phosphatases have been identified in T cells and shown to regulate T-cell responses. This review focuses on the roles of the two cytoplasmic PTPs, the Src-homology 2 domain (SH2)-containing SHP-1 and SHP-2, in T-cell signaling, development, differentiation, and function.
引用
收藏
页码:342 / 359
页数:18
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