Endomembrane GPCR signaling: 15 years on, the quest continues

被引:1
|
作者
Calebiro, Davide [1 ,2 ]
Miljus, Tamara [1 ,2 ]
O'Brien, Shannon [1 ,2 ]
机构
[1] Univ Birmingham, Coll Med & Hlth, Dept Metab & Syst Sci, Birmingham, England
[2] Univ Birmingham & Nottingham, Ctr Membrane Prot & Receptors COMPARE, Birmingham, England
基金
英国惠康基金;
关键词
PROTEIN-COUPLED RECEPTORS; ADENYLATE-CYCLASE; CLATHRIN ADAPTER; CAMP; TRAFFICKING; ENDOCYTOSIS; ARRESTIN; PKA; MITOCHONDRIA; ACTIVATION;
D O I
10.1016/j.tibs.2024.10.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:46 / 60
页数:15
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