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Dynamic phospholipid signaling by G protein-coupled receptors

机译:G蛋白偶联受体的动态磷脂信号传导

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摘要

G protein-coupled receptors (GPCRs) control a variety of fundamental cellular processes by regulating phospholipid signaling pathways. Essential for signaling by a large number of receptors is the hydrolysis of the membrane phosphoinositide PIP2 by phospholipase C (PLC) into the second messengers IP3 and DAG. Many receptors also stimulate phospholipase D (PLD), leading to the generation of the versatile lipid, phosphatidic acid. Particular PLC and PLD isoforms take differential positions in receptor signaling and are additionally regulated by small GTPases of the Ras, Rho and ARF families. It is now recognized that the PLC substrate, PIP2, has signaling capacity by itself and can, by direct interaction, affect the activity and subcellular localization of PLD and several other proteins. As expected, the synthesis of PIP, by phosphoinositide 5-kinases is tightly regulated as well. In this review, we present an overview of how these signaling pathways are governed by GPCRs, explain the molecular basis for the spatially and temporally organized, highly dynamic quality of phospholipid signaling, and point to the functional connection of the pathways. (c) 2006 Elsevier B.V. All rights reserved.
机译:G蛋白偶联受体(GPCR)通过调节磷脂信号通路来控制多种基本细胞过程。大量受体发出信号所必需的是磷脂酶C(PLC)将膜磷酸肌醇PIP2水解为第二信使IP3和DAG。许多受体还刺激磷脂酶D(PLD),导致生成通用脂质,磷脂酸。特定的PLC和PLD亚型在受体信号传导中处于不同位置,并且还受Ras,Rho和ARF家族的小GTPases调节。现在已经认识到,PLC底物PIP2本身具有信号传递能力,并且可以通过直接相互作用来影响PLD和其他几种蛋白质的活性和亚细胞定位。如所期望的,磷酸肌醇5-激酶对PIP的合成也受到严格调节。在这篇综述中,我们概述了这些信号通路如何由GPCR调控,解释了磷脂信号在空间和时间上的组织,高动态质量的分子基础,并指出了这些通路的功能连接。 (c)2006 Elsevier B.V.保留所有权利。

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