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

期刊

SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
卷 15, 期 2, 页码 183-197

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcdb.2003.12.024

关键词

1-phosphatidylinositol 3-kinase; PI3K; B lymphocyte; second messenger; signal transduction

资金

  1. NIAID NIH HHS [AI-50831] Funding Source: Medline

向作者/读者索取更多资源

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.

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