Duodenal cytochrome b (Cybrd 1) and HIF-2α expression during acute hypoxic exposure in mice

Eur J Nutr. 2011 Dec;50(8):699-704. doi: 10.1007/s00394-011-0175-6. Epub 2011 Feb 27.

Abstract

Background: Recent evidence suggests that the duodenum can regulate iron absorption independently of hepcidin via the transcription factor Hif-2α acting directly on the transcription of the proteins involved in the iron transport. The current study investigates the temporal relationship between Dcytb and Hif-2α during early hypoxic stimulus in the enterocyte in vivo.

Methods: Duodenal Dcytb and Hif-2α protein expression was analysed by Western blot technique while gene regulation was determined by quantitative PCR.

Results: Both Dcytb and Hif-2α protein expression were increased during the first hours of hypoxic duration. A change in hepcidin expression however, was significant only at 72 h hypoxia. Increased iron absorption reported in early hypoxia could be accounted for in part by the enhancement of Dcytb expression by Hif-2α in the duodenum.

Conclusion: Modulation of Hif-2α predominates over hepcidin in the regulation of intestinal iron absorption during short hypoxic duration. The intestine exerts regulatory mechanisms in the dietary absorption of iron into systemic circulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimicrobial Cationic Peptides / metabolism
  • Basic Helix-Loop-Helix Transcription Factors / genetics*
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Blotting, Western
  • Cytochrome b Group / genetics*
  • Cytochrome b Group / metabolism
  • Duodenum / metabolism
  • Enterocytes / metabolism
  • Gene Expression Regulation*
  • Hepcidins
  • Hypoxia / metabolism*
  • Intestinal Absorption / genetics
  • Iron, Dietary / pharmacokinetics
  • Male
  • Mice
  • Oxidoreductases / genetics*
  • Oxidoreductases / metabolism

Substances

  • Antimicrobial Cationic Peptides
  • Basic Helix-Loop-Helix Transcription Factors
  • Cytochrome b Group
  • Hamp protein, mouse
  • Hepcidins
  • Iron, Dietary
  • endothelial PAS domain-containing protein 1
  • Oxidoreductases
  • Cybrd1 protein, mouse