Circadian clock molecule REV-ERBα regulates lung fibrotic progression through collagen stabilization

Nat Commun. 2023 Mar 9;14(1):1295. doi: 10.1038/s41467-023-36896-0.

Abstract

Molecular clock REV-ERBα is central to regulating lung injuries, and decreased REV-ERBα abundance mediates sensitivity to pro-fibrotic insults and exacerbates fibrotic progression. In this study, we determine the role of REV-ERBα in fibrogenesis induced by bleomycin and Influenza A virus (IAV). Bleomycin exposure decreases the abundance of REV-ERBα, and mice dosed with bleomycin at night display exacerbated lung fibrogenesis. Rev-erbα agonist (SR9009) treatment prevents bleomycin induced collagen overexpression in mice. Rev-erbα global heterozygous (Rev-erbα Het) mice infected with IAV showed augmented levels of collagens and lysyl oxidases compared with WT-infected mice. Furthermore, Rev-erbα agonist (GSK4112) prevents collagen and lysyl oxidase overexpression induced by TGFβ in human lung fibroblasts, whereas the Rev-erbα antagonist exacerbates it. Overall, these results indicate that loss of REV-ERBα exacerbates the fibrotic responses by promoting collagen and lysyl oxidase expression, whereas Rev-erbα agonist prevents it. This study provides the potential of Rev-erbα agonists in the treatment of pulmonary fibrosis.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Circadian Clocks* / genetics
  • Circadian Rhythm / physiology
  • Collagen
  • Humans
  • Lung / metabolism
  • Mice
  • Nuclear Receptor Subfamily 1, Group D, Member 1 / genetics
  • Nuclear Receptor Subfamily 1, Group D, Member 1 / metabolism
  • Protein-Lysine 6-Oxidase
  • Pulmonary Fibrosis* / chemically induced
  • Pulmonary Fibrosis* / genetics

Substances

  • Collagen
  • Nuclear Receptor Subfamily 1, Group D, Member 1
  • Protein-Lysine 6-Oxidase