Hypoxia-inducible factor-1α is required for transforming growth factor-β1-induced type I collagen, periostin and α-smooth muscle actin expression in human periodontal ligament cells

Arch Oral Biol. 2014 Jun;59(6):595-600. doi: 10.1016/j.archoralbio.2014.03.003. Epub 2014 Mar 19.

Abstract

Background: We reported previously that hypoxia inducible factor (HIF)-1α was not degraded under normoxic condition with transforming growth factor (TGF)-β1 stimulation in human periodontal ligament (PDL) cells; however, the role of HIF-1α has been unclear. Recently, HIF-1α, working together with TGF-β1, has been reported to promote extracellular matrix accumulation under normoxic condition in renal epithelial cell. The aim of this study is to investigate the effects of HIF-1α on the expression of TGF-β1-mediated genes including type I collagen, periostin and α-smooth muscle actin (SMA) in human PDL cells.

Methods: The effects of TGF-β1 on HIF-1α mRNA and protein expression were analyzed by real-time RT-PCR and western blot, respectively. Next, The expression of type I collagen, periostin and α-SMA mRNA were analyzed with or without HIF-1α under normoxic condition with TGF-β1 stimulation using a real-time RT-PCR.

Results: TGF-β1 induced the expression of HIF-1α both in mRNA and protein levels. TGF-β1-induced mRNA expression of type I collagen, periostin and α-SMA were inhibited even with TGF-β1 stimulation when HIF-1α was knocked down.

Conclusion: HIF-1α is required for TGF-β1-induced type I collagen, periostin and α-SMA expression in human PDL cells.

Keywords: HIF-1α; Periodontal ligament cells; TGF-β1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Bicuspid
  • Blotting, Western
  • Cell Adhesion Molecules / metabolism
  • Cell Culture Techniques
  • Collagen Type I / metabolism*
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism*
  • Muscle, Smooth / metabolism
  • Periodontal Ligament / cytology*
  • Periodontal Ligament / metabolism*
  • RNA, Messenger / metabolism
  • Real-Time Polymerase Chain Reaction
  • Transforming Growth Factor beta / pharmacology*

Substances

  • Actins
  • Cell Adhesion Molecules
  • Collagen Type I
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • POSTN protein, human
  • RNA, Messenger
  • Transforming Growth Factor beta