Eiger Dylan Scott, Hicks Chloe, Gardner Julia, Pham Uyen, Rajagopal Sudarshan
Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Harvard Medical School, Boston, Massachusetts, USA.
Bioessays. 2023 Nov;45(11):e2300123. doi: 10.1002/bies.202300123. Epub 2023 Aug 25.
G protein-coupled receptors (GPCRs) are the largest family of transmembrane receptors and primarily signal through two main effector proteins: G proteins and β-arrestins. Many agonists of GPCRs promote "biased" responses, in which different cellular signaling pathways are activated with varying efficacies. The mechanisms underlying biased signaling have not been fully elucidated, with many potential "hidden variables" that regulate this behavior. One contributor is "location bias," which refers to the generation of unique signaling cascades from a given GPCR depending upon the cellular location at which the receptor is signaling. Here, we review evidence that GPCRs are expressed at and traffic to various subcellular locations and discuss how location bias can impact the pharmacologic properties and characterization of GPCR agonists. We also evaluate how differences in subcellular environments can modulate GPCR signaling, highlight the physiological significance of subcellular GPCR signaling, and discuss the therapeutic potential of exploiting GPCR location bias.
G蛋白偶联受体(GPCRs)是最大的跨膜受体家族,主要通过两种主要效应蛋白进行信号传导:G蛋白和β-抑制蛋白。许多GPCR激动剂会促进“偏向性”反应,即不同的细胞信号通路以不同的效率被激活。偏向性信号传导的潜在机制尚未完全阐明,存在许多调节这种行为的潜在“隐藏变量”。其中一个因素是“位置偏向性”,它指的是特定GPCR根据其信号传导的细胞位置产生独特的信号级联反应。在此,我们综述了GPCR在各种亚细胞位置表达和转运的证据,并讨论位置偏向性如何影响GPCR激动剂的药理特性和表征。我们还评估亚细胞环境的差异如何调节GPCR信号传导,强调亚细胞GPCR信号传导的生理意义,并讨论利用GPCR位置偏向性的治疗潜力。