The Wave complex controls epidermal morphogenesis and proliferation by suppressing Wnt-Sox9 signaling

J Cell Biol. 2019 Apr 1;218(4):1390-1406. doi: 10.1083/jcb.201807216. Epub 2019 Mar 13.

Abstract

Development of the skin epidermis requires tight spatiotemporal control over the activity of several signaling pathways; however, the mechanisms that orchestrate these events remain poorly understood. Here, we identify a key role for the Wave complex proteins ABI1 and Wave2 in regulating signals that control epidermal shape and growth. In utero RNAi-mediated silencing of Abi1 or Wasf2 induced cellular hyperproliferation and defects in architecture of the interfollicular epidermis (IFE) and delayed hair follicle growth. Unexpectedly, SOX9, a hair follicle growth regulator, was aberrantly expressed throughout the IFE of the mutant embryos, and its forced overexpression mimicked the Wave complex loss-of-function phenotype. Moreover, Wnt signaling, which regulates SOX9+ cell specification, was up-regulated in Wave complex loss-of-function IFE. Importantly, we show that the Wave complex regulates filamentous actin content and that a decrease in actin levels is sufficient to elevate Wnt/β-catenin signaling. Our results identify a novel role for Wave complex- and actin-regulated signaling via Wnt and SOX9 in skin development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism*
  • Animals
  • Cell Proliferation*
  • Cells, Cultured
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / metabolism*
  • Epidermis / abnormalities
  • Epidermis / metabolism*
  • Gene Expression Regulation, Developmental
  • Gene Silencing
  • Hair Follicle / abnormalities
  • Hair Follicle / metabolism
  • Keratinocytes / metabolism*
  • Mice
  • Morphogenesis
  • Phosphorylation
  • SOX9 Transcription Factor / genetics
  • SOX9 Transcription Factor / metabolism*
  • Wiskott-Aldrich Syndrome Protein Family / genetics
  • Wiskott-Aldrich Syndrome Protein Family / metabolism*
  • Wnt Signaling Pathway*
  • beta Catenin / metabolism

Substances

  • Abi1 protein, mouse
  • Adaptor Proteins, Signal Transducing
  • CTNNB1 protein, mouse
  • Cytoskeletal Proteins
  • SOX9 Transcription Factor
  • Sox9 protein, mouse
  • Wasf2 protein, mouse
  • Wiskott-Aldrich Syndrome Protein Family
  • beta Catenin