Axonal Growth and Regeneration Group, German Center for Neurodegenerative Diseases (DZNE), Venusberg-Campus 1, Building 99, 53127 Bonn, Germany.
Biotech Research & Innovation Centre, University of Copenhagen, Ole Maaløes Vej 5, 2200 Copenhagen, Denmark.
Curr Biol. 2019 Nov 18;29(22):3874-3886.e9. doi: 10.1016/j.cub.2019.09.040. Epub 2019 Oct 31.
The specification of an axon and its subsequent outgrowth are key steps during neuronal polarization, a prerequisite to wire the brain. The Rho-guanosine triphosphatase (GTPase) RhoA is believed to be a central player in these processes. However, its physiological role has remained undefined. Here, genetic loss- and gain-of-function experiments combined with time-lapse microscopy, cell culture, and in vivo analysis show that RhoA is not involved in axon specification but confines the initiation of neuronal polarization and axon outgrowth during development. Biochemical analysis and super-resolution microscopy together with molecular and pharmacological manipulations reveal that RhoA restrains axon growth by activating myosin-II-mediated actin arc formation in the growth cone to prevent microtubules from protruding toward the leading edge. Through this mechanism, RhoA regulates the duration of axon growth and pause phases, thus controlling the tightly timed extension of developing axons. Thereby, this work unravels physiologically relevant players coordinating actin-microtubule interactions during axon growth.
轴突的特化及其随后的延伸是神经元极化过程中的关键步骤,这是大脑布线的前提。Rho 鸟苷三磷酸酶(GTPase)RhoA 被认为是这些过程中的核心参与者。然而,其生理作用仍未得到明确界定。在这里,遗传功能丧失和获得实验结合延时显微镜、细胞培养和体内分析表明,RhoA 不参与轴突特化,但限制了神经元极化和轴突延伸的起始发育。生化分析和超分辨率显微镜以及分子和药理学操作表明,RhoA 通过激活生长锥中的肌球蛋白 II 介导的肌动蛋白弧形成来抑制轴突生长,以防止微管向前缘突出。通过这种机制,RhoA 调节轴突生长和暂停阶段的持续时间,从而控制发育中轴突的紧密定时延伸。因此,这项工作揭示了在轴突生长过程中协调肌动蛋白-微管相互作用的生理相关因子。