Sposini Silvia, Hanyaloglu Aylin C
Institute of Reproductive and Developmental Biology, Dept. Surgery and Cancer, Imperial College London, UK.
Institute of Reproductive and Developmental Biology, Dept. Surgery and Cancer, Imperial College London, UK.
Biochem Pharmacol. 2017 Nov 1;143:1-9. doi: 10.1016/j.bcp.2017.04.028. Epub 2017 Apr 27.
Within any cellular signaling system membrane trafficking is a critical mechanism for cells to translate complex networks into specific downstream responses, including the signal pathways activated by the superfamily of G protein-coupled receptors (GPCRs). Classically, membrane trafficking is viewed as a mechanism to regulate ligand sensitivity of a target tissue by controlling the level of surface receptors. Recent studies, however, have not only highlighted that GPCR trafficking is a tightly regulated process critical for spatio-temporal control of signaling, but that heterotrimeric G protein signaling can also be reactivated or continue to signal from distinct endocytic compartments, and even endosomal microdomains. The significance of spatio-temporal control will be discussed, not only with respect to how these novel molecular pathways impact our basic understanding of cellular regulation, but also our view of how aberrant signaling can result in disease. Furthermore, these mechanisms offer the potential application for novel therapeutic strategies to identify GPCR compounds with high specificity in their actions.
在任何细胞信号系统中,膜运输都是细胞将复杂网络转化为特定下游反应的关键机制,包括由G蛋白偶联受体(GPCR)超家族激活的信号通路。传统上,膜运输被视为一种通过控制表面受体水平来调节靶组织配体敏感性的机制。然而,最近的研究不仅强调了GPCR运输是一个严格调控的过程,对信号的时空控制至关重要,而且异源三聚体G蛋白信号也可以从不同的内吞区室甚至内体微区重新激活或继续发出信号。本文将讨论时空控制的重要性,不仅涉及这些新的分子途径如何影响我们对细胞调节的基本理解,还涉及我们对异常信号如何导致疾病的看法。此外,这些机制为识别作用具有高特异性的GPCR化合物的新型治疗策略提供了潜在应用。