Heme oxygenase-1 attenuates epithelial-to-mesenchymal transition of human peritoneal mesothelial cells

Clin Exp Nephrol. 2013 Apr;17(2):284-93. doi: 10.1007/s10157-012-0699-y. Epub 2012 Nov 14.

Abstract

Background: Epithelial-to-mesenchymal transition (EMT) of peritoneal mesothelial cells has been regarded as an early mechanism of peritoneal fibrosis. A substantial and rapidly growing literature indicates that HO-1 provides the provenance for pathways that can interrupt virtually all major mechanisms of tissue injury. The effects of HO-1 expression on EMT, which plays a critical role in the development of peritoneal membrane (PM) fibrosis, are unknown and its roles in peritoneal fibrosis has not been studied, yet.

Methods: A piece of human omentum obtained from consenting patients undergoing elective abdominal surgery was used for study. We treated the human peritoneal mesothelial cells (HPMCs) with high glucose solution and HO-1 inducer (hemin, 10 μmol/L). To further investigate the pure effect of HO-1 on EMT of mesothelium, gene transfer of recombinant Adenovirus-harboring human HO-1 (Adv-HO-1 gene) to HPMCs was done.

Results: Exposure of HPMCs to HG solution resulted in an increase of the expression of mesenchymal markers such as α-smooth muscle actin (α-SMA) and was associated with a decrease in the expression of epithelial markers, E-cadherin. HO-1 protein expression was decreased in the same situation. Treatment of HPMCs with HO-1 inducer, hemin showed a dosage-dependent amelioration of HG induced changes in markers of EMT with increase of expression of HO-1. Human HO-1 gene transfection resulted in a significant increase in HO-1 expression and ameliorated HG-induced changes in expression of E-cadherin and α-SMA.

Conclusion: Taken together, our results suggest that HO-1 has a critical role in the modulation of peritoneal fibrosis, and, more important, the suppression of EMT. This study is the first to show the beneficial effect of HO-1 on reversing EMT in MC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Cadherins / metabolism
  • Dependovirus / genetics
  • Enzyme Induction / drug effects
  • Epithelial Cells / physiology*
  • Epithelial-Mesenchymal Transition / physiology*
  • Fibrosis
  • Gene Transfer Techniques
  • Genetic Vectors / genetics
  • Glucose / pharmacology
  • Heme Oxygenase-1 / biosynthesis
  • Heme Oxygenase-1 / genetics
  • Heme Oxygenase-1 / physiology*
  • Hemin / pharmacology
  • Humans
  • Immunohistochemistry
  • Peritoneum / cytology
  • Peritoneum / drug effects
  • Peritoneum / pathology
  • Plasmids / genetics
  • Polymerase Chain Reaction
  • Transforming Growth Factor beta1 / metabolism

Substances

  • ACTA2 protein, human
  • Actins
  • Cadherins
  • Transforming Growth Factor beta1
  • Hemin
  • Heme Oxygenase-1
  • Glucose