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In this study, we demonstrate that VDR is essential for the morphogenetic processes that drive hair cycle growth and cell division in the hair follicle (HF). We identify Vdr as a crucial regulator of catagen by demonstrating that the cKO phenotype of Vdr is the result of decreased apoptosis in the epithelial strands that are dying in the hair follicle during the catagen phase. This delay in the entrance of the HF into anagen can lead to alopecia. It also transforms the HF into a dermal cyst comprised of epidermal cells.
We used functional annotation enrichment analyses to look for potential VDR targets in order to understand the role of VDR during catagen. Comparing control CO fibroblasts with the VDR unliganded fibroblasts, we discovered that 268 genes are upregulated and 1,25D-dependent activation is downregulated. The majority of these genes are upregulated by WT fibroblasts.
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