Regulation of glycolysis in brown adipocytes by HIF-1α

Sci Rep. 2017 Jun 22;7(1):4052. doi: 10.1038/s41598-017-04246-y.

Abstract

Brown adipose tissue takes up large amounts of glucose during cold exposure in mice and humans. Here we report an induction of glucose transporter 1 expression and increased expression of several glycolytic enzymes in brown adipose tissue from cold-exposed mice. Accordingly, these genes were also induced after β-adrenergic activation of cultured brown adipocytes, concomitant with accumulation of hypoxia inducible factor-1α (HIF-1α) protein levels. HIF-1α accumulation was dependent on uncoupling protein 1 and generation of mitochondrial reactive oxygen species. Expression of key glycolytic enzymes was reduced after knockdown of HIF-1α in mature brown adipocytes. Glucose consumption, lactate export and glycolytic capacity were reduced in brown adipocytes depleted of Hif-1α. Finally, we observed a decreased β-adrenergically induced oxygen consumption in Hif-1α knockdown adipocytes cultured in medium with glucose as the only exogenously added fuel. These data suggest that HIF-1α-dependent regulation of glycolysis is necessary for maximum glucose metabolism in brown adipocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes, Brown / drug effects
  • Adipocytes, Brown / metabolism*
  • Adrenergic beta-Agonists / pharmacology
  • Animals
  • Cells, Cultured
  • Cold Temperature
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation, Enzymologic / drug effects
  • Glucose / metabolism*
  • Glucose Transport Proteins, Facilitative / genetics
  • Glucose Transport Proteins, Facilitative / metabolism
  • Glycolysis / drug effects
  • Glycolysis / genetics
  • Hypoxia
  • Hypoxia-Inducible Factor 1, alpha Subunit / genetics*
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism
  • Male
  • Mice
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Models, Biological
  • Thermogenesis / drug effects
  • Thermogenesis / genetics

Substances

  • Adrenergic beta-Agonists
  • Glucose Transport Proteins, Facilitative
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Glucose