AI Article Synopsis

  • Brown adipose tissue increases glucose uptake during cold exposure in mice and humans, linked to heightened expression of glucose transporter 1 and glycolytic enzymes.
  • Activation of β-adrenergic receptors in cultured brown adipocytes also raises HIF-1α levels, which are essential for supporting these metabolic processes.
  • Depleting HIF-1α in brown adipocytes decreases glycolytic activity, glucose consumption, and oxygen usage, highlighting its crucial role in glucose metabolism in these cells.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481455PMC
http://dx.doi.org/10.1038/s41598-017-04246-yDOI Listing

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