RhoA Controls Axon Extension Independent of Specification in the Developing Brain

Curr Biol. 2019 Nov 18;29(22):3874-3886.e9. doi: 10.1016/j.cub.2019.09.040. Epub 2019 Oct 31.

Abstract

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.

Keywords: RhoA; actin arcs; axon growth; axon specification; cytoskeleton dynamics; growth cone; microtubule protrusion; myosin II; neuronal polarity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin Cytoskeleton / metabolism
  • Actins / metabolism
  • Animals
  • Axons / metabolism*
  • Axons / physiology
  • Brain / embryology
  • Brain / metabolism
  • Cell Polarity / physiology
  • Female
  • Gain of Function Mutation / genetics
  • Growth Cones / metabolism
  • Loss of Function Mutation / genetics
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Microtubules / metabolism
  • Myosin Type II / metabolism
  • Neurogenesis / physiology
  • Neurons / metabolism
  • rhoA GTP-Binding Protein / genetics*
  • rhoA GTP-Binding Protein / metabolism*
  • rhoA GTP-Binding Protein / physiology

Substances

  • Actins
  • Myosin Type II
  • RhoA protein, mouse
  • rhoA GTP-Binding Protein