Takeo Yutaka, Kurabayashi Nobuhiro, Nguyen Minh Dang, Sanada Kamon
Department of Biophysics and Biochemistry, Graduate School of Science, The University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan.
Molecular Genetics Research Laboratory, Graduate School of Science, The University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan.
Sci Rep. 2016 May 4;6:25180. doi: 10.1038/srep25180.
The ability of radial glial progenitors (RGPs) to generate cortical neurons is determined by local extracellular factors and signaling pathways intrinsic to RGPs. Here we find that GPR157, an orphan G protein-coupled receptor, localizes to RGPs' primary cilia exposed to the cerebrospinal fluid (CSF). GPR157 couples with Gq-class of the heterotrimeric G-proteins and signals through IP3-mediated Ca(2+) cascade. Activation of GPR157-Gq signaling enhances neuronal differentiation of RGPs whereas interfering with GPR157-Gq-IP3 cascade in RGPs suppresses neurogenesis. We also detect the presence of putative ligand(s) for GPR157 in the CSF, and demonstrate the increased ability of the CSF to activate GPR157 at neurogenic phase. Thus, GPR157-Gq signaling at the primary cilia of RGPs is activated by the CSF and contributes to neurogenesis.
放射状胶质前体细胞(RGPs)生成皮质神经元的能力由局部细胞外因子和RGPs内在的信号通路决定。我们发现,孤儿G蛋白偶联受体GPR157定位于暴露于脑脊液(CSF)的RGPs的初级纤毛上。GPR157与异源三聚体G蛋白的Gq类偶联,并通过IP3介导的Ca(2+)级联信号传导。GPR157-Gq信号的激活增强了RGPs的神经元分化,而干扰RGPs中的GPR157-Gq-IP3级联则抑制神经发生。我们还在脑脊液中检测到GPR157的假定配体的存在,并证明脑脊液在神经发生阶段激活GPR157的能力增强。因此,CSF激活了RGPs初级纤毛上的GPR157-Gq信号,并促进了神经发生。