溶血磷脂酸和鞘氨醇-磷酸G蛋白偶联受体的信号传导机制和分子特征。

S An, E J Goetzl, H Lee
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引用次数: 0

摘要

溶血磷脂酸(LPA)和鞘磷脂1-磷酸(S1P)是有效的磷脂介质,具有多种生物活性。它们的外观和功能特性表明它们可能在发育、伤口愈合和组织再生中起作用。LPA和S1P具有刺激生长等复杂的生物活性,部分原因是激活了多种G蛋白介导的细胞内信号通路。几种异三聚体G蛋白,以及Ras-和rho -依赖通路在LPA和S1P的细胞反应中起核心作用。最近,一些由内皮分化基因家族(edg)编码的G蛋白偶联受体已被证明可以结合LPA或S1P,并转导cAMP、Ca2+、MAP激酶、Rho和基因转录的反应。本文综述了我们目前对LPA和S1P细胞反应的关键信号通路的理解以及Edg受体的分子生物学分析的最新进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Signaling mechanisms and molecular characteristics of G protein-coupled receptors for lysophosphatidic acid and sphingosine 1-phosphate.

Lysophosphatidic acid (LPA) and sphingosine 1-phosphate (S1P) are potent phospholipid mediators with diverse biological activities. Their appearance and functional properties suggest possible roles in development, wound healing, and tissue regeneration. The growth-stimulating and other complex biological activities of LPA and S1P are attributable in part to the activation of multiple G protein-mediated intracellular signaling pathways. Several heterotrimeric G proteins, as well as Ras- and Rho-dependent pathways play central roles in the cellular responses to LPA and S1P. Recently, several G protein-coupled receptors encoded by a family of endothelial differentiation genes (edg) have been shown to bind LPA or S1P and transduce responses of cAMP, Ca2+, MAP kinases, Rho, and gene transcription. This review summarizes our current understanding of signaling pathways critical for cellular responses to LPA and S1P and of recent progress in the molecular biological analyses of the Edg receptors.

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