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分子生物学与生物技术综述:G蛋白偶联受体介导的跨膜信号转导

Reviews in molecular biology and biotechnology: transmembrane signaling by G protein-coupled receptors.

作者信息

Luttrell Louis M

机构信息

Division of Endocrinology, Diabetes and Medical Genetics, Department of Medicine, Medical University of South Carolina, 96 Jonathan Lucas Street, 816 CSB, P.O. Box 250624, Charleston, SC 29425, USA.

出版信息

Mol Biotechnol. 2008 Jul;39(3):239-64. doi: 10.1007/s12033-008-9031-1. Epub 2008 Feb 1.

Abstract

As the most diverse type of cell surface receptor, the importance heptahelical G protein-coupled receptors (GPCRs) to clinical medicine cannot be overestimated. Visual, olfactory and gustatory sensation, intermediary metabolism, cell growth and differentiation are all influenced by GPCR signals. The basic receptor-G protein-effector mechanism of GPCR signaling is tuned by a complex interplay of positive and negative regulatory events that amplify the effect of a hormone binding the receptor or that dampen cellular responsiveness. The association of heptahelical receptors with a variety of intracellular partners other than G proteins has led to the discovery of potential mechanisms of GPCR signaling that extend beyond the classical paradigms. While the physiologic relevance of many of these novel mechanisms of GPCR signaling remains to be established, their existence suggests that the mechanisms of GPCR signaling are even more diverse than previously imagined.

摘要

作为细胞表面受体中种类最多样的类型,七螺旋G蛋白偶联受体(GPCRs)对临床医学的重要性无论怎样高估都不为过。视觉、嗅觉和味觉感受、中间代谢、细胞生长和分化均受GPCR信号的影响。GPCR信号传导的基本受体-G蛋白-效应器机制通过正向和负向调节事件的复杂相互作用进行调节,这些调节事件可放大激素与受体结合的效应或减弱细胞反应性。七螺旋受体与G蛋白以外的多种细胞内伴侣的关联,已促成了GPCR信号传导潜在机制的发现,这些机制超出了经典模式。虽然GPCR信号传导的许多这些新机制的生理相关性仍有待确定,但其存在表明GPCR信号传导机制比以前想象的更加多样。

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