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

机译:G蛋白偶联受体串扰:多种受体信号传导途径的微调。

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摘要

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.
机译:通过大家族的G蛋白偶联受体(GPCR)发出的信号可以导致许多细胞反应,从调节细胞内cAMP水平到刺激基因转录。根据主要与之相互作用的特定G蛋白亚型,该受体家族的成员已分为不同类别。因此,与GS蛋白偶联的受体会刺激许多细胞中的腺苷酸环化酶,而与Gq / 11偶联的受体可以通过激活磷脂酶C来动员细胞内Ca2 +。可以在平行但独立的途径内放大细胞内信号传导。在本文中,Lisa Selbie和Stephen Hill回顾了这些协同相互作用的一些证据,并提出它们可能在微调来自多个受体信号通路的信号中起重要作用。

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