UNC Neuroscience Center and the Department of Cell Biology and Physiology, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA; Division of Neurogenetics, National Institute of Genetics, Mishima 411-8540, Japan; Department of Genetics, SOKENDAI (The Graduate University for Advanced Studies), Mishima 411-8540, Japan.
UNC Neuroscience Center and the Department of Cell Biology and Physiology, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA.
Neuron. 2019 Sep 4;103(5):836-852.e5. doi: 10.1016/j.neuron.2019.05.049. Epub 2019 Jul 2.
Polarized, non-overlapping, regularly spaced, tiled organization of radial glial cells (RGCs) serves as a framework to generate and organize cortical neuronal columns, layers, and circuitry. Here, we show that mediator of cell motility 1 (Memo1) is a critical determinant of radial glial tiling during neocortical development. Memo1 deletion or knockdown leads to hyperbranching of RGC basal processes and disrupted RGC tiling, resulting in aberrant radial unit assembly and neuronal layering. Memo1 regulates microtubule (MT) stability necessary for RGC tiling. Memo1 deficiency leads to disrupted MT minus-end CAMSAP2 distribution, initiation of aberrant MT branching, and altered polarized trafficking of key basal domain proteins such as GPR56, and thus aberrant RGC tiling. These findings identify Memo1 as a mediator of RGC scaffold tiling, necessary to generate and organize neurons into functional ensembles in the developing cerebral cortex.
极化、不重叠、规则间隔、平铺排列的放射状胶质细胞(RGC)组织作为生成和组织皮层神经元柱、层和回路的框架。在这里,我们表明,细胞运动介质 1(Memo1)是新皮层发育过程中放射状胶质细胞平铺的关键决定因素。Memo1 的缺失或敲低导致 RGC 基底过程的过度分支和 RGC 平铺的破坏,导致异常的放射状单位组装和神经元分层。Memo1 调节微管(MT)稳定性,这对于 RGC 平铺是必需的。Memo1 缺乏导致 MT 负端 CAMSAP2 分布中断,异常 MT 分支的开始,以及关键基底域蛋白(如 GPR56)的极化运输改变,从而导致 RGC 平铺异常。这些发现表明 Memo1 是 RGC 支架平铺的介质,对于在发育中的大脑皮层中将神经元生成并组织成功能单元是必需的。