Okkenhaug Klaus, Ali Khaled, Vanhaesebroeck Bart
Laboratory of Lymphocyte Signalling and Development, Babraham Institute, Cambridge, UK, CB2 4AT.
Trends Immunol. 2007 Feb;28(2):80-7. doi: 10.1016/j.it.2006.12.007. Epub 2007 Jan 5.
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 Cgamma (PLCgamma)-mediated hydrolysis of PtdIns(4,5)P(2), resulting in the activation of Ras, protein kinase C and Ca(2+) 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 PtdIns(4,5)P(2) to yield phosphatidylinositol(3,4,5)-trisphosphate, activating signalling pathways that overlap with PLCgamma 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 p110delta 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 p110delta in regulating antigen-dependent responses in these cell types.
抗原受体的激活触发了两条源自磷脂酰肌醇(4,5)-二磷酸[PtdIns(4,5)P₂]的重要信号通路。第一条是磷脂酶Cγ(PLCγ)介导的PtdIns(4,5)P₂水解,导致Ras、蛋白激酶C激活以及Ca²⁺内流。这最终导致基因表达和效应细胞反应发生深刻变化,包括分泌颗粒胞吐作用和细胞因子产生。相比之下,磷酸肌醇3-激酶(PI3K)将PtdIns(4,5)P₂磷酸化生成磷脂酰肌醇(3,4,5)-三磷酸,激活与PLCγ重叠或PI3K特异性的信号通路。PI3K特异性的信号通路包括Akt介导的Foxo转录因子失活以及葡萄糖摄取和代谢的非转录调控。PI3K的p110δ亚型是B细胞、T细胞和肥大细胞识别抗原后PI3K活性的主要来源。在此,我们综述了p110δ在调节这些细胞类型中抗原依赖性反应的作用。