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内膜G蛋白偶联受体信号传导:15年过去了,探索仍在继续。

Endomembrane GPCR signaling: 15 years on, the quest continues.

作者信息

Calebiro Davide, Miljus Tamara, O'Brien Shannon

机构信息

Department of Metabolism and Systems Science, College of Medicine and Health, University of Birmingham, Birmingham, UK; Centre of Membrane Proteins and Receptors (COMPARE), Universities of Birmingham and Nottingham, Birmingham, UK.

Department of Metabolism and Systems Science, College of Medicine and Health, University of Birmingham, Birmingham, UK; Centre of Membrane Proteins and Receptors (COMPARE), Universities of Birmingham and Nottingham, Birmingham, UK.

出版信息

Trends Biochem Sci. 2025 Jan;50(1):46-60. doi: 10.1016/j.tibs.2024.10.006. Epub 2024 Nov 11.

DOI:10.1016/j.tibs.2024.10.006
PMID:39532582
Abstract

G-protein-coupled receptors (GPCRs) are the largest family of cell receptors. They mediate the effects of a multitude of endogenous and exogenous cues, are deeply involved in human physiology and disease, and are major pharmacological targets. Whereas GPCRs were long thought to signal exclusively at the plasma membrane, research over the past 15 years has revealed that they also signal via classical G-protein-mediated pathways on membranes of intracellular organelles such as endosomes and the Golgi complex. This review provides an overview of recent advances and emerging concepts related to endomembrane GPCR signaling, as well as ongoing research aimed at a better understanding of its mechanisms, physiological relevance, and potential therapeutic applications.

摘要

G蛋白偶联受体(GPCRs)是细胞受体中最大的家族。它们介导多种内源性和外源性信号的作用,深度参与人体生理和疾病过程,并且是主要的药理学靶点。长期以来,人们一直认为GPCRs仅在质膜上进行信号传导,但过去15年的研究表明,它们也通过经典的G蛋白介导途径在细胞内细胞器(如内体和高尔基体复合体)的膜上进行信号传导。本综述概述了与内膜GPCR信号传导相关的最新进展和新兴概念,以及旨在更好地理解其机制、生理相关性和潜在治疗应用的正在进行的研究。

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