Protein tyrosine phosphorylation in T cell signaling

被引:74
作者
Mustelin, T
Abraham, RT
Rudd, CE
Alonso, A
Merlo, JJ
机构
[1] Burnham Inst, Ctr Canc Res, Program Signal Transduct, La Jolla, CA 92037 USA
[2] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Canc Immunol & AIDS, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2002年 / 7卷
关键词
Review; T cell activation; Lck; Fyn; c-Yes; Syk; ZAP-70; Itk; Txk; CD45; HePTP; PEP; PTP-MEG2; PTPH1; PTP-MEG1; PTP36; PTEN; LMPTP; PLCgamma1; SLP-76; LAT; FYB; SLAP-130; Vav-1; PI3K; c-Cbl; TSAd; SAP; SH2D1A; TRIM;
D O I
10.2741/musteli1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This review discusses in considerable detail the tyrosine phosphorylation events that couple the T cell antigen receptor to downstream signaling pathways. First, the protein kinases that catalyze these tyrosine phosphorylation are introduced, then the phosphatases that mediate removal of phosphate from tyrosine residues. Next, we discuss the molecular clock work by which these enzymes initiated T cell activation. Finally, we briefly review the key substrates for tyrosine phosphorylation and their role in coupling the kinases and phosphatases to gene transcription and other aspects of the T lymphocyte response to antigen.
引用
收藏
页码:D918 / D969
页数:52
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