Inverse correlation between metallothioneins and hypoxia-inducible factor 1 alpha in colonocytes and experimental colitis

Biochem Biophys Res Commun. 2011 Dec 16;416(3-4):307-12. doi: 10.1016/j.bbrc.2011.11.031. Epub 2011 Nov 15.

Abstract

A positive-feedback mechanism between hypoxia-inducible factor 1 alpha (HIF-1α) and metallothioneins (MTs) has been identified in different diseases. Both proteins have been independently proposed in the pathogenesis of inflammatory bowel disease (IBD); however, their relation has never been studied in the gut. In this study, we investigated the interaction between HIF-1α and MTs in colonic epithelial cells and during experimental colitis. Dimethyloxalylglycine (DMOG) was used to subject colonocytes to hydroxylase inhibition and HIF-1α stabilization in three experimental models (in vitro, in vivo and ex vivo). Small interfering RNA targeting HIF-1α (siRNA-HIF) and MT (siRNA-MT) together with zinc-mediated MT induction were used to study the interaction between HIF-1α and MT in HT29 cells. Acute colitis was induced in C57BL/6 mice using dextran sulphate sodium. MT expression and HIF-1α protein levels were measured using quantitative real-time PCR and ELISA, respectively. Vascular endothelial growth factor (VEGF) expression was quantified as an indirect measure of HIF-1 transcriptional activity. DMOG down-regulated MT expression in HT29 cells, in freshly isolated human colonocytes and in colonocytes isolated from mice treated with DMOG (p<0.05). SiRNA-HIF-treated cells displayed significant higher basal MT levels (p<0.05) and an attenuated MT down-regulation after DMOG treatment. In turn, HIF-1α stabilization was significantly lower in zinc-treated control cells, displaying high MT levels, compared to siRNA-MT cells treated with DMOG (p<0.05). In the course of experimental colitis, MT and VEGF mRNA expression were inversely related. MTs were induced in the acute phase and down-regulated during recovery. Opposing results were observed for VEGF expression levels (p<0.05). The present study underscores the inverse relation between HIF-1α and MT expression in colonocytes and during experimental colitis. The manipulation of MTs may represent a novel therapeutic strategy for patients suffering from IBD.

MeSH terms

  • Amino Acids, Dicarboxylic / pharmacology
  • Animals
  • Colitis / chemically induced
  • Colon / drug effects
  • Colon / metabolism*
  • Down-Regulation
  • HT29 Cells
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / genetics
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism*
  • Inflammatory Bowel Diseases / chemically induced
  • Inflammatory Bowel Diseases / metabolism*
  • Metallothionein / genetics
  • Metallothionein / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Models, Animal
  • RNA, Small Interfering / genetics
  • Vascular Endothelial Growth Factor A / genetics
  • Vascular Endothelial Growth Factor A / metabolism
  • Zinc / pharmacology

Substances

  • Amino Acids, Dicarboxylic
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • RNA, Small Interfering
  • Vascular Endothelial Growth Factor A
  • Metallothionein
  • Zinc
  • oxalylglycine