Vitamin D/VDR signaling induces miR-27a/b expression in oral lichen planus

Sci Rep. 2020 Jan 15;10(1):301. doi: 10.1038/s41598-019-57288-9.

Abstract

MicroRNA-27a/b are small non-coding RNAs which are reported to regulate inflammatory response and cell proliferation. Although some studies have demonstrated that miR-27b is down-regulated in the oral specimens of patients suffering with oral lichen planus (OLP), the molecular mechanism of miR-27b decrease remains a large mystery, and the expression of miR-27a in OLP is not well explored. Here, we demonstrated both miR-27a and miR-27b, compared with healthy controls, were reduced in the oral biopsies, serum and saliva samples derived from OLP patients. The reductions of miR-27a/b were also confirmed in the lipopolysaccharide (LPS)- or activated CD4+ T cell-treated human oral keratinocytes (HOKs). Furthermore, we found vitamin D receptor (VDR) binding sites in the promoters of miR-27a/b genes and verified this finding. We also tested miR-27a/b levels in the oral epithelium from paricalcitol-treated, vitamin D deficient or VDR knockout mice. In the rescue experiments, we confirmed vitamin D and VDR inhibited LPS- or activated CD4+ T cell-induced miR-27a/b reductions in HOKs. In sum, our results show that vitamin D/VDR signaling induces miR-27a/b in oral lichen planus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding Sites
  • Case-Control Studies
  • Disease Models, Animal
  • Down-Regulation / drug effects
  • Epithelial Cells / cytology
  • Epithelial Cells / metabolism
  • Ergocalciferols / pharmacology
  • Humans
  • Keratinocytes / cytology
  • Keratinocytes / drug effects
  • Keratinocytes / metabolism
  • Lichen Planus, Oral / metabolism
  • Lichen Planus, Oral / pathology
  • Lipopolysaccharides / pharmacology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • MicroRNAs / blood
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Promoter Regions, Genetic
  • Receptors, Calcitriol / deficiency
  • Receptors, Calcitriol / genetics
  • Receptors, Calcitriol / metabolism*
  • Signal Transduction* / drug effects
  • Vitamin D / metabolism*

Substances

  • Ergocalciferols
  • Lipopolysaccharides
  • MIRN27 microRNA, human
  • MicroRNAs
  • Receptors, Calcitriol
  • Vitamin D
  • paricalcitol