N-WASP-Arp2/3 signaling controls multiple steps of dendrite maturation in Purkinje cells in vivo

Development. 2022 Dec 1;149(23):dev201214. doi: 10.1242/dev.201214. Epub 2022 Dec 5.

Abstract

During neural development, the actin filament network must be precisely regulated to form elaborate neurite structures. N-WASP tightly controls actin polymerization dynamics by activating an actin nucleator Arp2/3. However, the importance of N-WASP-Arp2/3 signaling in the assembly of neurite architecture in vivo has not been clarified. Here, we demonstrate that N-WASP-Arp2/3 signaling plays a crucial role in the maturation of cerebellar Purkinje cell (PC) dendrites in vivo in mice. N-WASP was expressed and activated in developing PCs. Inhibition of Arp2/3 and N-WASP from the beginning of dendrite formation severely disrupted the establishment of a single stem dendrite, which is a characteristic basic structure of PC dendrites. Inhibition of Arp2/3 after stem dendrite formation resulted in hypoplasia of the PC dendritic tree. Cdc42, an upstream activator of N-WASP, is required for N-WASP-Arp2/3 signaling-mediated PC dendrite maturation. In addition, overactivation of N-WASP is also detrimental to dendrite formation in PCs. These findings reveal that proper activation of N-WASP-Arp2/3 signaling is crucial for multiple steps of PC dendrite maturation in vivo.

Keywords: Actin; Arp2/3; Dendrite; Maturation; Mouse; N-WASP; Purkinje cell.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin Cytoskeleton / metabolism
  • Actin-Related Protein 2-3 Complex* / genetics
  • Actin-Related Protein 2-3 Complex* / metabolism
  • Animals
  • Dendrites / metabolism
  • Mice
  • Neurogenesis / genetics
  • Purkinje Cells* / metabolism
  • Wiskott-Aldrich Syndrome Protein, Neuronal* / genetics
  • Wiskott-Aldrich Syndrome Protein, Neuronal* / metabolism

Substances

  • Wiskott-Aldrich Syndrome Protein, Neuronal
  • Actin-Related Protein 2-3 Complex