Huang Yung-An, Hsu Chih-Hsuan, Chiu Ho-Chieh, Hsi Pei-Yu, Ho Chris T, Lo Wei-Lun, Hwang Eric
Department of Biological Science and Technology, National Chiao Tung University, Hsinchu, Taiwan 30068.
Institute of Molecular Medicine and Bioengineering, National Chiao Tung University, Hsinchu, Taiwan 30068.
J Cell Sci. 2020 May 14;133(9):jcs241992. doi: 10.1242/jcs.241992.
Microtubules (MTs) are the most abundant cytoskeleton in neurons, and control multiple facets of their development. While the MT-organizing center (MTOC) in mitotic cells is typically located at the centrosome, the MTOC in neurons switches to non-centrosomal sites. A handful of cellular components have been shown to promote non-centrosomal MT (ncMT) formation in neurons, yet the regulation mechanism remains unknown. Here, we demonstrate that the small GTPase Ran is a key regulator of ncMTs in neurons. Using an optogenetic tool that enables light-induced local production of RanGTP, we demonstrate that RanGTP promotes ncMT plus-end growth along the neurite. Additionally, we discovered that actin waves drive the anterograde transport of RanGTP. Pharmacological disruption of actin waves abolishes the enrichment of RanGTP and reduces growing ncMT plus-ends at the neurite tip. These observations identify a novel regulation mechanism for ncMTs and pinpoint an indirect connection between the actin and MT cytoskeletons in neurons.
微管(MTs)是神经元中最丰富的细胞骨架,控制着神经元发育的多个方面。虽然有丝分裂细胞中的微管组织中心(MTOC)通常位于中心体,但神经元中的MTOC会转移到非中心体部位。已有少数细胞成分被证明可促进神经元中非中心体微管(ncMT)的形成,但其调控机制仍不清楚。在这里,我们证明小GTP酶Ran是神经元中ncMT的关键调节因子。使用一种光遗传学工具,能够光诱导局部产生RanGTP,我们证明RanGTP促进ncMT沿神经突的正端生长。此外,我们发现肌动蛋白波驱动RanGTP的顺向运输。肌动蛋白波的药理学破坏消除了RanGTP的富集,并减少了神经突尖端生长的ncMT正端。这些观察结果确定了一种新的ncMT调控机制,并指出了神经元中肌动蛋白和微管细胞骨架之间的间接联系。