PI3K signaling controls cell fate at many points in B lymphocyte development and activation

被引:56
作者
Donahue, AC [1 ]
Fruman, DA [1 ]
机构
[1] Univ Calif Irvine, Dept Mol Biol & Biochem, Irvine, CA 92697 USA
关键词
1-phosphatidylinositol; 3-kinase; PI3K; B lymphocyte; second messenger; signal transduction;
D O I
10.1016/j.semcdb.2003.12.024
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Many receptors on diverse cell types activate phosphoinositide 3-kinase (PI3K). The lipid products of PI3K, termed 3-phosphoinositides, regulate numerous cellular processes by recruiting specific proteins to membrane signaling complexes. In the B lymphocyte lineage, PI3K activation is a critical control point at various stages of development, proliferation and differentiation. PI3K signaling is promoted by stimulatory receptors such as surface immunoglobulin, CD40, Toll-like receptors and cytokine receptors, and opposed by the inhibitory receptor FcgammaRIIB1. Genetic dissection of the PI3K pathway in mice has indicated that certain B cell functions are regulated by a limited set of PI3K isoforms and downstream effectors. Here we review our current understanding of how signals are relayed to and from PI3K in B cells. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:183 / 197
页数:15
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