Regulation of B cell signal transduction by SH2-containing protein-tyrosine phosphatases

被引:57
作者
Siminovitch, KA
Neel, BG
机构
[1] Univ Toronto, Dept Med, Toronto, ON M5G 1X5, Canada
[2] Univ Toronto, Dept Immunol, Toronto, ON M5G 1X5, Canada
[3] Univ Toronto, Dept Mol & Med Genet, Toronto, ON M5G 1X5, Canada
[4] Mt Sinai Hosp, SLRI, Toronto, ON M5G 1X5, Canada
[5] Beth Israel Deaconess Med Ctr, Dept Med, Div Hematol Oncol, Canc Biol Program,HIM 1047, Boston, MA 02215 USA
关键词
auto-immunity; B lymphocytes; co-receptors; protein-tyrosine phosphatases; signal transduction;
D O I
10.1006/smim.1998.0125
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tyrosyl phosphorylation plays a key rob in B lymphocyte signaling: The mechanisms by which protein tyrosine kinases (PTKs) regulate signaling pathways in B cells have been investigated extensively. More recently, attention has turned to the protein-tyrosine phosphatases (PTPs), particularly those containing SH2 domains. SHP-1 has been shown to be a critical regulator of antigen receptor signaling, acting, at least in part, via inhibitory co-receptors containing SHP-1 binding sites. These studies have been aided considerably by the analysis of mice carrying naturally-arising mutations in the SHP-1 gene as well as mice bearing targeted mutations in other components of B cell signaling pathways. The function of SHP-2 in B cells is less clear although studies in other cell systems suggests that it may play a signal-enhancing role.
引用
收藏
页码:329 / 347
页数:19
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