Rudolf Virchow Center, DFG-Research Center for Experimental Biomedicine, University of Würzburg, Würzburg, Germany.
J Mol Endocrinol. 2010 Jul;45(1):1-8. doi: 10.1677/JME-10-0014. Epub 2010 Apr 8.
G protein-coupled receptors (GPCRs) are the largest family of plasma membrane receptors. They mediate the effects of several endogenous cues and serve as important pharmacological targets. Although many biochemical events involved in GPCR signaling have been characterized in great detail, little is known about their spatiotemporal dynamics in living cells. The recent advent of optical methods based on fluorescent resonance energy transfer allows, for the first time, to directly monitor GPCR signaling in living cells. Utilizing these methods, it has been recently possible to show that the receptors for two protein/peptide hormones, the TSH and the parathyroid hormone, continue signaling to cAMP after their internalization into endosomes. This type of intracellular signaling is persistent and apparently triggers specific cellular outcomes. Here, we review these recent data and explain the optical methods used for such studies. Based on these findings, we propose a revision of the current model of the GPCR-cAMP signaling pathway to accommodate receptor signaling at endosomes.
G 蛋白偶联受体(GPCRs)是最大的一类细胞膜受体。它们介导多种内源性信号的作用,并作为重要的药理学靶点。尽管 GPCR 信号转导涉及的许多生化事件已经被详细描述,但对于它们在活细胞中的时空动态知之甚少。最近出现的基于荧光共振能量转移的光学方法首次允许直接在活细胞中监测 GPCR 信号转导。利用这些方法,最近已经可以证明,两种蛋白质/肽激素(促甲状腺素和甲状旁腺激素)的受体在被内吞到内体后继续向 cAMP 传递信号。这种细胞内信号传递是持续的,显然会引发特定的细胞结果。在这里,我们回顾这些最新的数据,并解释用于这些研究的光学方法。基于这些发现,我们提出了对 GPCR-cAMP 信号通路的当前模型进行修订,以适应内体中的受体信号传递。