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G蛋白偶联受体的相互作用:多条受体信号通路的精细调节

G protein-coupled-receptor cross-talk: the fine-tuning of multiple receptor-signalling pathways.

作者信息

Selbie L A, Hill S J

机构信息

Institute of Cell Signalling, University of Nottingham, Queen's Medical Centre, Medical School, UK.

出版信息

Trends Pharmacol Sci. 1998 Mar;19(3):87-93. doi: 10.1016/s0165-6147(97)01166-8.

Abstract

Signalling via the large family of G protein-coupled receptors (GPCRs) can lead to many cellular responses, ranging from regulation of intracellular levels of cAMP to stimulation of gene transcription. Members of this receptor family have been grouped into different categories dependent on the particular G protein subtypes that they predominantly interact with. Thus, receptors that couple to GS proteins will stimulate adenylate cyclase in many cells, while Gq/11-coupled receptors can mobilize intracellular Ca2+ via activation of phospholipase C. There is accumulating evidence, however, that activation of one particular signalling pathway by a GPCR can amplify intracellular signalling within a parallel but separate pathway. In this article Lisa Selbie and Stephen Hill review some of the evidence for these synergistic interactions and suggest that they may have an important role in finetuning signals from multiple receptor signalling pathways.

摘要

通过G蛋白偶联受体(GPCR)大家族进行的信号传导可引发多种细胞反应,范围从细胞内cAMP水平的调节到基因转录的刺激。该受体家族的成员已根据它们主要相互作用的特定G蛋白亚型被分为不同类别。因此,与Gs蛋白偶联的受体将在许多细胞中刺激腺苷酸环化酶,而与Gq/11偶联的受体可通过激活磷脂酶C来动员细胞内的Ca2+。然而,越来越多的证据表明,GPCR对一种特定信号通路的激活可在平行但独立的通路内放大细胞内信号传导。在本文中,丽莎·塞尔比和斯蒂芬·希尔回顾了这些协同相互作用的一些证据,并表明它们可能在微调来自多个受体信号通路的信号方面发挥重要作用。

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