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G 蛋白偶联受体和 G 蛋白介导的内膜信号转导。

Endomembrane-Based Signaling by GPCRs and G-Proteins.

机构信息

Cardiovascular Research Institute, University of California San Francisco (UCSF), 555 Mission Bay Blvd., San Francisco, CA 94158, USA.

Istituto per L'endocrinologia e L'oncologia Sperimentale "Gaetano Salvatore" (IEOS)-Sede Secondaria, Via Pietro Castellino 111, 80131 Napoli, Italy.

出版信息

Cells. 2022 Feb 3;11(3):528. doi: 10.3390/cells11030528.

Abstract

G-protein-coupled receptors (GPCRs) and G-proteins have a range of roles in many physiological and pathological processes and are among the most studied signaling proteins. A plethora of extracellular stimuli can activate the GPCR and can elicit distinct intracellular responses through the activation of specific transduction pathways. For many years, biologists thought that GPCR signaling occurred entirely on the plasma membrane. However, in recent decades, many lines of evidence have proved that the GPCRs and G-proteins may reside on endomembranes and can start or propagate signaling pathways through the organelles that form the secretory route. How these alternative intracellular signaling pathways of the GPCR and G-proteins influence the physiological and pathological function of the endomembranes is still under investigation. Here, we review the general role and classification of GPCRs and G-proteins with a focus on their signaling pathways in the membrane transport apparatus.

摘要

G 蛋白偶联受体 (GPCRs) 和 G 蛋白在许多生理和病理过程中发挥着多种作用,是研究最多的信号蛋白之一。大量的细胞外刺激可以激活 GPCR,并通过激活特定的转导途径引起不同的细胞内反应。多年来,生物学家认为 GPCR 信号转导完全发生在质膜上。然而,近几十年来,许多证据证明 GPCRs 和 G 蛋白可能位于内质网上,并且可以通过形成分泌途径的细胞器开始或传播信号通路。这些 GPCR 和 G 蛋白的替代细胞内信号通路如何影响内质网的生理和病理功能仍在研究中。在这里,我们回顾了 GPCRs 和 G 蛋白的一般作用和分类,并重点介绍了它们在膜转运装置中的信号通路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6604/8834376/3dfdb4f39689/cells-11-00528-g001.jpg

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