腺苷酸环化酶
G蛋白
Gsα亚单位
cAMP依赖途径
信号转导
G蛋白偶联受体
细胞生物学
受体
第二信使系统
GTP结合蛋白调节剂
GTPase激活蛋白
异三聚体G蛋白
生物
化学
生物化学
作者
Raissa Perrault,Peter Zahradka
出处
期刊:Current Vascular Pharmacology
[Bentham Science]
日期:2014-04-01
卷期号:12 (2): 258-270
标识
DOI:10.2174/1570161112666140226122512
摘要
G protein signaling is an extremely complex event that is involved in almost every cellular process. As such, G protein-coupled receptors are the most commonly found type of transmembrane receptors used by cells to initiate intracellular signaling events. However, the widely accepted model of cyclical GDP-GTP exchange in response to ligand binding to 7TMRs, followed by dissociation of the G protein subunits and activation of intracellular signaling cascades, has repeatedly been challenged in recent years. Some of the exceptions that have been brought forth include signaling by a non-dissociated, rearranged heterotrimer and the existence of “reverse-mode”, active G proteins that interact with active receptors. Here, we focus on Gαi/o, one of the common Gα classes, and outline a major exception to the classical model, that of G protein coupling to RTKs. We then describe a novel concept in Gαi/o signaling, namely that the pathways induced by agonist binding circumvent the typical signaling pathways responsive to decreases in the second messenger cAMP, via adenylyl cyclase inhibition. Keywords: Adenylyl-cyclase independent, Gαi, G protein-coupled receptors, receptor tyrosine kinase.
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