Biological Effects of CYP11A1-Derived Vitamin D and Lumisterol Metabolites in the Skin

J Invest Dermatol. 2024 Oct;144(10):2145-2161. doi: 10.1016/j.jid.2024.04.022. Epub 2024 Jul 12.

Abstract

Novel pathways of vitamin D3, lumisterol 3 (L3), and tachysterol 3 (T3) activation have been discovered, initiated by CYP11A1 and/or CYP27A1 in the case of L3 and T3. The resulting hydroxymetabolites enhance protection of skin against DNA damage and oxidative stress; stimulate keratinocyte differentiation; exert anti-inflammatory, antifibrogenic, and anticancer activities; and inhibit cell proliferation in a structure-dependent manner. They act on nuclear receptors, including vitamin D receptor, aryl hydrocarbon receptor, LXRα/β, RAR-related orphan receptor α/γ, and peroxisome proliferator-activated receptor-γ, with selectivity defined by their core structure and distribution of hydroxyl groups. They can activate NRF2 and p53 and inhibit NF-κB, IL-17, Shh, and Wnt/β-catenin signaling. Thus, they protect skin integrity and physiology.

Keywords: Lumisterol; Nuclear receptors; Skin; Tachysterol; Vitamin D receptors.

Publication types

  • Review

MeSH terms

  • Animals
  • Cell Proliferation / drug effects
  • Cholecalciferol / metabolism
  • Cholecalciferol / pharmacology
  • Cholestanetriol 26-Monooxygenase / genetics
  • Cholestanetriol 26-Monooxygenase / metabolism
  • Humans
  • Keratinocytes / drug effects
  • Keratinocytes / metabolism
  • Oxidative Stress / drug effects
  • Signal Transduction / drug effects
  • Skin* / drug effects
  • Skin* / metabolism
  • Vitamin D / analogs & derivatives
  • Vitamin D / metabolism
  • Vitamin D / pharmacology

Substances

  • Cholestanetriol 26-Monooxygenase
  • Vitamin D
  • Cholecalciferol
  • CYP27A1 protein, human