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Arrestins as rheostats of GPCR signalling

机译:逮捕作为GPCR信令的变温镜

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G protein-coupled receptors (GPCRs) have a central role in a myriad of physiological functions and their dysregulation underlies some of the most prevalent human diseases. They control cell behaviour and cell fate by recruiting and activating intracellular molecules such as heterotrimeric G proteins and arrestins, both of which take active roles in GPCR signalling. G proteins have been viewed as the main signal transducers, whereas arrestins were originally associated with signalling desensitization. Nevertheless, some studies have demonstrated G protein-independent roles of arrestins in GPCR signal transduction. In this Comment, we highlight recent key findings obtained with genome-edited cells to suggest that arrestins - rather than being active transducers in their own right - are key modulators of G protein-initiated signal transmission, thereby shaping and fine-tuning dynamic GPCR responses in space and time.
机译:G蛋白偶联受体(GPCR)在无数的生理功能中具有核心作用,并且它们的失呼算术基于一些最普遍的人类疾病。 它们通过募集和激活细胞内分子等诸如异映上的G蛋白和捕获素来控制细胞行为和细胞命运,这两者都在GPCR信号传导中采取活性作用。 G蛋白已被视为主要信号换能器,而捕获素最初与信号传导脱敏相关。 然而,一些研究表明,GPCR信号转导中的R蛋白无关作用。 在此评论中,我们突出了最近通过基因组编辑的细胞获得的主要发现,表明逮捕素 - 而不是在自己的右侧是活跃的传感器 - 是G蛋白引发的信号传输的关键调节剂,从而形成和微调动态GPCR响应 在空间和时间。

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