Msx2 Supports Epidermal Competency during Wound-Induced Hair Follicle Neogenesis

J Invest Dermatol. 2018 Sep;138(9):2041-2050. doi: 10.1016/j.jid.2018.02.043. Epub 2018 Mar 23.

Abstract

Cutaneous wounds in adult mammals typically heal by scarring. However, large full-thickness wounds undergo wound-induced hair follicle neogenesis (WIHN), a form of regeneration. Here, we show that WIHN requires transient expression of epidermal Msx2 in two phases: the wound margin early and the wound center late. Msx2 expression is present in the migrating epithelium during early wound healing and then presents in the epithelium and mesenchyme later in the wound center. WIHN is abrogated in germline and epithelial-specific Msx2 mutant mice. Unlike the full-length Msx2 promoter, a minimal Msx2 promoter fails activation in the wound center, suggesting complex regulation of Msx2 expression. The Msx2 promoter binding sites include Tcf/Lef, Jun/Creb, Pax3, and three SMAD sites. However, basal epithelial-induced BMP suppression by noggin overexpression did not affect WIHN. We propose that Msx2 signaling is required for the epidermis to acquire spatiotemporal competence during WIHN. Topologically, hair regeneration dominates in the wound center, coinciding with late Msx2 expression. Together, these results suggest that intrinsic Msx2 expression supports epithelial competency during hair follicle neogenesis. This work provides insight into endogenous mechanisms modulating competency of adult epidermal progenitors for mammalian ectodermal appendage neogenesis, and offers the target Msx2 for future regeneration-promoting therapies.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Disease Models, Animal
  • Gene Expression Regulation*
  • Hair Follicle / metabolism
  • Hair Follicle / pathology*
  • Homeodomain Proteins / biosynthesis
  • Homeodomain Proteins / genetics*
  • Mice, Inbred C57BL
  • Mice, SCID
  • RNA / genetics
  • Regeneration / physiology*
  • Signal Transduction
  • Skin / injuries*
  • Skin / metabolism
  • Skin / pathology
  • Wound Healing / genetics*
  • Wounds and Injuries / complications*
  • Wounds and Injuries / genetics
  • Wounds and Injuries / metabolism

Substances

  • Homeodomain Proteins
  • MSX2 protein
  • RNA