Non-hypoxic induction of HIF-3alpha by 2-deoxy-D-glucose and insulin

Biochem Biophys Res Commun. 2007 Jan 12;352(2):437-43. doi: 10.1016/j.bbrc.2006.11.027. Epub 2006 Nov 16.

Abstract

Hypoxia-inducible factors (HIFs) are key mediators of cellular adaptation to hypoxia, but also respond to non-hypoxic stimuli. To clarify involvement in metabolic disturbances, HIFs were characterised in rats subjected to insulin-induced hypoglycaemia or cellular glucoprivation provoked by 2-deoxy-D-glucose (2-DG). Using real-time qPCR, organ-specific expression of HIF-1alpha, -2alpha, -3alpha, -1beta, and of the target gene GLUT-1 was determined. Distribution of HIF-3alpha proteins was examined by immunohistochemistry. Both, insulin and 2-DG resulted in a widespread increase in HIF-3alpha mRNA. HIF-2alpha mRNA increased in lung and heart after 2-DG only, whereas other HIFs remained unaffected. A pronounced increase of protein levels in cerebral cortex was observed for HIF-3alpha. Functional significance of HIF induction was reflected in enhancement of GLUT-1 mRNA. Transcriptional up-regulation of HIF-3alpha represents a typical response to in vivo hypoglycaemia and glucoprivation. These data suggest an involvement of the HIF system in metabolic derangements as for instance caused by diabetes.

MeSH terms

  • Animals
  • Apoptosis Regulatory Proteins
  • Cells, Cultured
  • Deoxyglucose / administration & dosage*
  • Dose-Response Relationship, Drug
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / physiology
  • Hippocampus / drug effects
  • Hippocampus / metabolism*
  • Hypoxia / metabolism
  • Insulin / administration & dosage*
  • Male
  • Mice
  • Organ Specificity
  • Rats
  • Rats, Wistar
  • Repressor Proteins
  • Tissue Distribution
  • Transcription Factors / metabolism*

Substances

  • Apoptosis Regulatory Proteins
  • Hif3a protein, mouse
  • Insulin
  • Repressor Proteins
  • Transcription Factors
  • Deoxyglucose