Department of Ophthalmology, University of California, San Francisco, San Francisco, CA.
Department of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA.
J Cell Biol. 2018 May 7;217(5):1847-1868. doi: 10.1083/jcb.201709041. Epub 2018 Feb 26.
A diffusion barrier at the transition zone enables the compartmentalization of signaling molecules by cilia. The BBSome and the small guanosine triphosphatase Arl6, which triggers BBSome coat polymerization, are required for the exit of activated signaling receptors from cilia, but how diffusion barriers are crossed when membrane proteins exit cilia remains to be determined. In this study, we found that activation of the ciliary G protein-coupled receptors (GPCRs) Smoothened and SSTR3 drove the Arl6-dependent assembly of large, highly processive, and cargo-laden retrograde BBSome trains. Single-molecule imaging revealed that the assembly of BBSome trains enables the lateral transport of ciliary GPCRs across the transition zone. However, the removal of activated GPCRs from cilia was inefficient because a second periciliary diffusion barrier was infrequently crossed. We conclude that exit from cilia is a two-step process in which BBSome/Arl6 trains first move activated GPCRs through the transition zone before a periciliary barrier can be crossed.
在过渡区的扩散屏障使纤毛分隔信号分子。BBSome 和小鸟苷三磷酸酶 Arl6,触发 BBSome 外壳聚合,是从纤毛中退出激活的信号受体所必需的,但当膜蛋白退出纤毛时如何穿过扩散屏障仍有待确定。在这项研究中,我们发现纤毛 G 蛋白偶联受体(GPCR)Smoothened 和 SSTR3 的激活驱动了 Arl6 依赖性的大型、高连续性和富含货物的逆行 BBSome 列车的组装。单分子成像显示,BBSome 列车的组装使纤毛 GPCR 的侧向转运能够穿过过渡区。然而,从纤毛中去除激活的 GPCR 效率不高,因为第二个纤毛周围的扩散屏障很少被穿过。我们的结论是,纤毛退出是一个两步过程,其中 BBSome/Arl6 列车首先将激活的 GPCR 穿过过渡区,然后才能穿过纤毛周围的屏障。