Jiang Tao, Zhang Guowei, Liang Yaozhong, Cai Zhenbin, Liang Zhi, Lin Hongsheng, Tan Minghui
Department of Orthopaedics, the First Affiliated Hospital of Jinan University, Guangzhou 510630, China.
Department of Orthopaedics, the First Affiliated Hospital of Jinan University, Guangzhou 510630, China.
Neuroscience. 2020 May 10;434:83-92. doi: 10.1016/j.neuroscience.2020.02.008. Epub 2020 Feb 14.
Plexin family proteins mediate semaphorin signalling during dendritic arbour development. However, the role of PlexinA3 in the growth of dendrites of cultured cerebellar granule neurons (CGNs) is not known. We found that PlexinA3 colocalizes with CRMP2 (collapsin response mediator protein 2) in dendritic shafts. Immunoprecipitation and glutathione transferase pulldown assays showed that the intracellular Ras-binding domain of PlexinA3 directly interacts with CRMP2. PlexinA3 was necessary and sufficient for the growth of CGN dendrites, as genetic knockdown of PlexinA3 reduced but its overexpression increased dendritic lengths and dendritic tip numbers. These increases were enhanced with CRMP2 overexpression and abolished with CRMP2 knockdown, indicating that CRMP2 is the downstream effector. Furthermore, PlexinA3/CRMP2 signalling contributed to Sema3A-controlled dendritic growth. Together, these data identify a novel PlexinA3/CRMP2 pathway in semaphorin-regulated growth of cultured CGN dendrites.
在树突状分支发育过程中,丛状蛋白家族蛋白介导信号素信号传导。然而,丛状蛋白A3在培养的小脑颗粒神经元(CGN)树突生长中的作用尚不清楚。我们发现丛状蛋白A3与CRMP2(塌陷反应介导蛋白2)在树突轴中共定位。免疫沉淀和谷胱甘肽转移酶下拉实验表明,丛状蛋白A3的细胞内Ras结合结构域直接与CRMP2相互作用。丛状蛋白A3对于CGN树突的生长是必需且充分的,因为丛状蛋白A3的基因敲低会减少树突长度和树突尖端数量,而其过表达则会增加这些指标。CRMP2过表达会增强这些增加,而CRMP2敲低则会消除这些增加,表明CRMP2是下游效应器。此外,丛状蛋白A3/CRMP2信号传导有助于信号素3A控制的树突生长。总之,这些数据确定了在信号素调节的培养CGN树突生长中的一种新的丛状蛋白A3/CRMP2途径。