Androgens modify Wnt agonists/antagonists expression balance in dermal papilla cells preventing hair follicle stem cell differentiation in androgenetic alopecia

Mol Cell Endocrinol. 2017 Jan 5:439:26-34. doi: 10.1016/j.mce.2016.10.018. Epub 2016 Oct 18.

Abstract

In androgenetic alopecia, androgens impair dermal papilla-induced hair follicle stem cell (HFSC) differentiation inhibiting Wnt signaling. Wnt agonists/antagonists balance was analyzed after dihydrotestosterone (DHT) stimulation in androgen-sensitive dermal papilla cells (DPC) cultured as spheroids or monolayer. In both culture conditions, DHT stimulation downregulated Wnt5a and Wnt10b mRNA while the Wnt antagonist Dkk-1 was upregulated. Notably, tissue architecture of DPC-spheroids lowers Dkk-1 and enhances Wnt agonists' basal expression; probably contributing to DPC inductivity. The role of Wnt agonists/antagonists as mediators of androgen inhibition of DPC-induced HFSC differentiation was evaluated. Inductive DPC-conditioned medium supplemented with DKK-1 impaired HFSC differentiation mimicking androgens' action. This effect was associated with inactivation of Wnt/β-catenin pathway in differentiating HFSC by both DPC-conditioned media. Moreover, addition of WNT10b to DPC-medium conditioned with DHT, overcame androgen inhibition of HFSC differentiation. Our results identify DKK1 and WNT10b as paracrine factors which modulate the HFSC differentiation inhibition involved in androgen-driven balding.

Keywords: Androgenetic alopecia; Dermal papilla; Epidermal stem cells; Epithelial-mesenchymal interactions; Wnt ligands.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alopecia / genetics
  • Alopecia / pathology*
  • Androgens / pharmacology*
  • Cell Differentiation / drug effects*
  • Cell Line
  • Culture Media, Conditioned / pharmacology
  • Cytoplasm / drug effects
  • Cytoplasm / metabolism
  • Hair Follicle / pathology*
  • Humans
  • Ligands
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Stem Cells / drug effects
  • Stem Cells / metabolism
  • Stem Cells / pathology*
  • Wnt Proteins / agonists*
  • Wnt Proteins / antagonists & inhibitors*
  • Wnt Signaling Pathway / drug effects
  • beta Catenin / metabolism

Substances

  • Androgens
  • Culture Media, Conditioned
  • Ligands
  • RNA, Messenger
  • Wnt Proteins
  • beta Catenin