Epithelium-mesenchyme interactions control the activity of peroxisome proliferator-activated receptor beta/delta during hair follicle development

Mol Cell Biol. 2005 Mar;25(5):1696-712. doi: 10.1128/MCB.25.5.1696-1712.2005.

Abstract

Hair follicle morphogenesis depends on a delicate balance between cell proliferation and apoptosis, which involves epithelium-mesenchyme interactions. We show that peroxisome proliferator-activated receptor beta/delta (PPARbeta/delta) and Akt1 are highly expressed in follicular keratinocytes throughout hair follicle development. Interestingly, PPARbeta/delta- and Akt1-deficient mice exhibit similar retardation of postnatal hair follicle morphogenesis, particularly at the hair peg stage, revealing a new important function for both factors in the growth of early hair follicles. We demonstrate that a time-regulated activation of the PPARbeta/delta protein in follicular keratinocytes involves the up-regulation of the cyclooxygenase 2 enzyme by a mesenchymal paracrine factor, the hepatocyte growth factor. Subsequent PPARbeta/delta-mediated temporal activation of the antiapoptotic Akt1 pathway in vivo protects keratinocytes from hair pegs against apoptosis, which is required for normal hair follicle development. Together, these results demonstrate that epithelium-mesenchyme interactions in the skin regulate the activity of PPARbeta/delta during hair follicle development via the control of ligand production and provide important new insights into the molecular biology of hair growth.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Cyclooxygenase 2
  • Epithelium / chemistry
  • Epithelium / growth & development
  • Epithelium / physiology
  • Hair Follicle / chemistry
  • Hair Follicle / cytology
  • Hair Follicle / growth & development*
  • Hepatocyte Growth Factor / genetics
  • Hepatocyte Growth Factor / physiology
  • Intercellular Signaling Peptides and Proteins / physiology
  • Keratinocytes / chemistry
  • Keratinocytes / cytology
  • Keratinocytes / physiology
  • Mesoderm / physiology*
  • Mice
  • Mice, Knockout
  • Models, Biological
  • Morphogenesis / genetics
  • Morphogenesis / physiology
  • PPAR delta / genetics
  • PPAR delta / metabolism*
  • PPAR delta / physiology
  • PPAR-beta / genetics
  • PPAR-beta / metabolism*
  • PPAR-beta / physiology
  • Paracrine Communication / physiology*
  • Phosphorylation
  • Prostaglandin-Endoperoxide Synthases / physiology
  • Protein Serine-Threonine Kinases / analysis
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism
  • Proto-Oncogene Proteins / analysis
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-akt

Substances

  • Intercellular Signaling Peptides and Proteins
  • PPAR delta
  • PPAR-beta
  • Proto-Oncogene Proteins
  • Hepatocyte Growth Factor
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-akt