Treat Anny Caceres, Wheeler David S, Stolz Donna B, Tsang Michael, Friedman Peter A, Romero Guillermo
Laboratory for GPCR Biology, Department of Pharmacology & Chemical Biology, University of Pittsburgh, Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States of America.
Medical Scientist Training Program, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States of America.
PLoS One. 2016 Apr 7;11(4):e0153144. doi: 10.1371/journal.pone.0153144. eCollection 2016.
Directional flow of the cerebrospinal fluid requires coordinated movement of the motile cilia of the ependymal epithelium that lines the cerebral ventricles. Here we report that mice lacking the Na+/H+ Exchanger Regulatory Factor 1 (NHERF1/Slc9a3r1, also known as EBP50) develop profound communicating hydrocephalus associated with fewer and disorganized ependymal cilia. Knockdown of NHERF1/slc9a3r1 in zebrafish embryos also causes severe hydrocephalus of the hindbrain and impaired ciliogenesis in the otic vesicle. Ultrastructural analysis did not reveal defects in the shape or organization of individual cilia. Similar phenotypes have been described in animals with deficiencies in Wnt signaling and the Planar Cell Polarity (PCP) pathway. We show that NHERF1 binds the PCP core genes Frizzled (Fzd) and Vangl. We further show that NHERF1 assembles a ternary complex with Fzd4 and Vangl2 and promotes translocation of Vangl2 to the plasma membrane, in particular to the apical surface of ependymal cells. Taken together, these results strongly support an important role for NHERF1 in the regulation of PCP signaling and the development of functional motile cilia.
脑脊液的定向流动需要衬于脑室的室管膜上皮运动纤毛的协调运动。我们在此报告,缺乏钠氢交换调节因子1(NHERF1/Slc9a3r1,也称为EBP50)的小鼠会出现严重的交通性脑积水,伴有室管膜纤毛数量减少和排列紊乱。在斑马鱼胚胎中敲低NHERF1/slc9a3r1也会导致后脑严重脑积水以及耳泡中的纤毛发生受损。超微结构分析未发现单个纤毛的形状或组织存在缺陷。在Wnt信号通路和平面细胞极性(PCP)通路存在缺陷的动物中也描述过类似的表型。我们发现NHERF1与PCP核心基因卷曲蛋白(Fzd)和Vangl结合。我们进一步表明,NHERF1与Fzd4和Vangl2组装形成三元复合物,并促进Vangl2转运至质膜,特别是室管膜细胞的顶端表面。综上所述,这些结果有力地支持了NHERF1在调节PCP信号通路和功能性运动纤毛发育中的重要作用。