Pal Kasturi, Hwang Sun-Hee, Somatilaka Bandarigoda, Badgandi Hemant, Jackson Peter K, DeFea Kathryn, Mukhopadhyay Saikat
Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305.
J Cell Biol. 2016 Mar 28;212(7):861-75. doi: 10.1083/jcb.201506132. Epub 2016 Mar 21.
Dynamic changes in membrane protein composition of the primary cilium are central to development and homeostasis, but we know little about mechanisms regulating membrane protein flux. Stimulation of the sonic hedgehog (Shh) pathway in vertebrates results in accumulation and activation of the effector Smoothened within cilia and concomitant disappearance of a negative regulator, the orphan G protein-coupled receptor (GPCR), Gpr161. Here, we describe a two-step process determining removal of Gpr161 from cilia. The first step involves β-arrestin recruitment by the signaling competent receptor, which is facilitated by the GPCR kinase Grk2. An essential factor here is the ciliary trafficking and activation of Smoothened, which by increasing Gpr161-β-arrestin binding promotes Gpr161 removal, both during resting conditions and upon Shh pathway activation. The second step involves clathrin-mediated endocytosis, which functions outside of the ciliary compartment in coordinating Gpr161 removal. Mechanisms determining dynamic compartmentalization of Gpr161 in cilia define a new paradigm for down-regulation of GPCRs during developmental signaling from a specialized subcellular compartment.
初级纤毛膜蛋白组成的动态变化对发育和体内平衡至关重要,但我们对调节膜蛋白通量的机制知之甚少。在脊椎动物中,刺激音猬因子(Shh)信号通路会导致效应蛋白Smoothened在纤毛内积累并激活,同时一种负调节因子——孤儿G蛋白偶联受体(GPCR)Gpr161会随之消失。在此,我们描述了一个决定Gpr161从纤毛中去除的两步过程。第一步涉及信号传导功能正常的受体招募β - 抑制蛋白,这一过程由GPCR激酶Grk2促进。这里的一个关键因素是Smoothened的纤毛运输和激活,它通过增加Gpr161与β - 抑制蛋白的结合来促进Gpr161的去除,无论是在静息状态还是Shh信号通路激活时。第二步涉及网格蛋白介导的内吞作用,它在纤毛区室之外发挥作用,协同Gpr161的去除。决定Gpr161在纤毛中动态区室化的机制为发育信号传导过程中从特定亚细胞区室对GPCR进行下调定义了一种新的模式。