The vitamin D receptor is required for activation of cwnt and hedgehog signaling in keratinocytes

Thomas S. Lisse, Vaibhav Saini, Hengguang Zhao, Hilary F. Luderer, Francesca Gori, Marie B. Demay

Research output: Contribution to journalArticlepeer-review

35 Scopus citations

Abstract

Alopecia (hair loss) in vitamin D receptor (VDR)-null mice is due to absence of ligand-independent actions of the VDR that are required for initiation of postmorphogenic hair cycles. Investigations were undertaken to determine whether the VDR is required for the induction of signaling pathways that play an important role in this process. The induction of cWnt and hedgehog target genes that characterizes early anagen was found to be dramatically attenuated in VDR-/- mice, relative to wild-type (WT) mice. To determine whether this reflects impaired responsiveness to cWnt ligands, in vitro studies were performed in primary keratinocytes. These studies demonstrated impaired induction of cWnt target genes in response to Wnt3a in VD-/- keratinocytes, relative to wild-type keratinocytes. Chromatin immunoprecipitation analyses revealed that the VDR was recruited to the regulatory regions of cWnt and hedgehog target genes in WT keratinocytes but not in VDR-/- or Lef1-/- keratinocytes. Lef1 was enriched on these same regulatory regions in WT keratinocytes but not in VDR-/- keratinocytes. In vivo studies were performed to determine whether activation of the hedgehog pathway could bypass the defect in cWnt signaling observed in the absence of the unliganded VDR. In WT, but not VDR-/-, mice, hedgehog agonist treatment resulted in an induction of cWnt and hedgehog target genes and the generation of mature anagen hair follicles. Thus, these studies demonstrate that the unliganded VDR interacts with regulatory regions in the cWnt and hedgehog target genes and is required for the induction of these pathways during the postnatal hair cycle.

Original languageEnglish (US)
Pages (from-to)1698-1706
Number of pages9
JournalMolecular Endocrinology
Volume28
Issue number10
DOIs
StatePublished - Oct 1 2014
Externally publishedYes

ASJC Scopus subject areas

  • Molecular Biology
  • Endocrinology

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