Antigen receptor signalling:: a distinctive role for the p110δ isoform of Pl3K

被引:101
作者
Okkenhaug, Klaus [1 ]
Ali, Khaled
Vanhaesebroeck, Bart
机构
[1] Babraham Inst, Lab Lymphocyte Signalling & Dev, Cambridge CB2 4AT, England
[2] Ludwig Inst Canc Res, London W1W 7BS, England
[3] UCL, Dept Biochem & Mol Biol, London WC1E 6BT, England
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1016/j.it.2006.12.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The activation of antigen receptors; triggers two important signalling pathways originating from phosphatidylinositol(4,5)-bisphosphate [PtdIns(4,5)P-2]. The first is phospholipase C gamma (PLC gamma) -mediated hydrolysis of PtdIns(4,5)P, resulting in the activation of Ras, protein kinase C and Ca2+, flux. This culminates in profound alterations in gene expression and effector-cell responses, including secretory granule exocytosis and cytokine production. By contrast, phosphoinositide 3-kinases (PI3Ks) phosphorylate Ptdlns(4,5)P-2 to yield phosphatidylinositol (3,4,5)-trisphosphate, activating signalling pathways that overlap with PLCy or are PI3K-specific. Pathways that are PI3K-specific include Akt-mediated inactivation of Foxo transcription factors and transcription-independent regulation of glucose uptake and metabolism. The p110 delta isoform of PI3K is the main source of PI3K activity following antigen recognition by B cells, T cells and mast cells. Here, we review the roles of p110 delta in regulating antigen-dependent responses in these cell types.
引用
收藏
页码:80 / 87
页数:8
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