Disturbed expression of vitamin D and retinoic acid-related orphan receptors α and γ and of megalin in inflammatory skin diseases

Exp Dermatol. 2022 May;31(5):781-788. doi: 10.1111/exd.14521. Epub 2022 Jan 13.

Abstract

The pathogenesis of inflammatory skin diseases is associated with the abnormal activity of keratinocytes and immune cells infiltrate. Vitamin D3 deficiency can correlate with the increased incidence, severity and duration of inflammatory skin disorders. The exact mechanism on how vitamin D3 influences inflammatory skin diseases still requires clarification. However, it can be associated with the disturbances in transmembrane glycoprotein-LRP2/megalin, which is implicated in vitamin D3 transport to the cell, and defects in vitamin D-signalling through the nuclear receptors. Therefore, by using immunohistochemistry, we analysed the expression of LRP2/megalin, VDR, RORα and RORγ in allergic contact dermatitis, lichen simplex chronicus, sarcoidosis and psoriasis in comparison with the normal skin. We observed decreased expression of LRP2/megalin in all inflammatory lesions in comparison with the normal skin. Significant differences were also noticed in VDR, RORα and RORγ levels between inflammatory lesions and normal skin. Our research indicates disturbed expression of LRP2/megalin, VDR, RORα and RORγ in inflammatory skin lesions in comparison with normal skin. Therefore, we suggest that changes in the activity of these proteins may play role in pathogenesis of inflammatory skin disorders. Furthermore, we suggest that LRP2/megalin, VDR, RORα and RORy may serve as targets in therapy of these diseases.

Keywords: allergic contact dermatitis; lichen simplex chronicus; megalin; nuclear receptors; psoriasis; sarcoidosis; vitamin D.

MeSH terms

  • Dermatitis*
  • Humans
  • Low Density Lipoprotein Receptor-Related Protein-2
  • Nuclear Receptor Subfamily 1, Group F, Member 1
  • Nuclear Receptor Subfamily 1, Group F, Member 3
  • Receptors, Calcitriol / metabolism
  • Retinoic Acid Receptor alpha
  • Tretinoin
  • Vitamin D* / metabolism
  • Vitamins

Substances

  • LRP2 protein, human
  • Low Density Lipoprotein Receptor-Related Protein-2
  • Nuclear Receptor Subfamily 1, Group F, Member 1
  • Nuclear Receptor Subfamily 1, Group F, Member 3
  • RORA protein, human
  • Receptors, Calcitriol
  • Retinoic Acid Receptor alpha
  • VDR protein, human
  • Vitamins
  • Vitamin D
  • Tretinoin