Effects of the PI3K/Akt signaling pathway on the hair inductivity of human dermal papilla cells in hair beads

J Biosci Bioeng. 2022 Jul;134(1):55-61. doi: 10.1016/j.jbiosc.2022.03.010. Epub 2022 Apr 14.

Abstract

Dermal papilla cells (DPCs), which play a central role in the regulation of hair follicle development and hair growth, are among the most promising cell sources for hair regenerative medicine. However, a critical issue in the use of DPCs is the immediate loss of hair inducing functions in typical two-dimensional (2D) culture. We have previously demonstrated that when DPCs are encapsulated in drops of collagen gel (named hair beads, HBs), the density of collagen and cells is concentrated >10-fold during 3 d of culture through the spontaneous constriction of the drops, leading to efficient hair follicle regeneration upon transplantation. However, the mechanisms responsible for the activation of the hair-inducing functions of DPCs have been poorly elucidated. Here, transcriptome comparisons of human DPCs in HB culture and in typical 2D culture revealed that the phosphoinositide 3-kinase and Akt (PI3K/Akt) signaling pathway was significantly upregulated in HB culture. Inhibition of the PI3K/Akt signaling pathway decreased the hair-inducing capability of DPCs in HBs, while the activation of the PI3K/Akt signaling pathway using an activator improved trichogenous gene expression of DPCs in 2D culture. These results suggest that the PI3K/Akt signaling pathway is crucial for the maintenance and restoration of hair inductivity of DPCs. HB culture and/or activators of the PI3K/Akt signaling pathway could be a promising strategy for preparing DPCs for hair regenerative medicine.

Keywords: Dermal papilla cells; Hair beads; Hair regenerative medicine; PI3K/Akt signaling pathway; SC79.

MeSH terms

  • Cell Proliferation
  • Cells, Cultured
  • Collagen
  • Hair
  • Hair Follicle* / cytology
  • Humans
  • Phosphatidylinositol 3-Kinase* / metabolism
  • Proto-Oncogene Proteins c-akt* / metabolism
  • Signal Transduction*

Substances

  • Collagen
  • Phosphatidylinositol 3-Kinase
  • Proto-Oncogene Proteins c-akt