Regulation of glycolysis in brown adipocytes by HIF-1α
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 wer...
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doaj-5cc8df8a3be24f4c90f043fd2f9aa2232020-12-08T00:40:50ZengNature Publishing GroupScientific Reports2045-23222017-06-017111510.1038/s41598-017-04246-yRegulation of glycolysis in brown adipocytes by HIF-1αAstrid L. Basse0Marie S. Isidor1Sally Winther2Nina B. Skjoldborg3Maria Murholm4Elise S. Andersen5Steen B. Pedersen6Christian Wolfrum7Bjørn Quistorff8Jacob B. Hansen9Department of Biology, University of CopenhagenDepartment of Biology, University of CopenhagenDepartment of Biology, University of CopenhagenDepartment of Biology, University of CopenhagenDepartment of Biology, University of CopenhagenDepartment of Biology, University of CopenhagenDepartment of Clinical Medicine, Aarhus UniversityInstitute of Food, Nutrition and Health, ETH ZurichDepartment of Biomedical Sciences, University of CopenhagenDepartment of Biology, University of CopenhagenAbstract 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.https://doi.org/10.1038/s41598-017-04246-y |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Astrid L. Basse Marie S. Isidor Sally Winther Nina B. Skjoldborg Maria Murholm Elise S. Andersen Steen B. Pedersen Christian Wolfrum Bjørn Quistorff Jacob B. Hansen |
spellingShingle |
Astrid L. Basse Marie S. Isidor Sally Winther Nina B. Skjoldborg Maria Murholm Elise S. Andersen Steen B. Pedersen Christian Wolfrum Bjørn Quistorff Jacob B. Hansen Regulation of glycolysis in brown adipocytes by HIF-1α Scientific Reports |
author_facet |
Astrid L. Basse Marie S. Isidor Sally Winther Nina B. Skjoldborg Maria Murholm Elise S. Andersen Steen B. Pedersen Christian Wolfrum Bjørn Quistorff Jacob B. Hansen |
author_sort |
Astrid L. Basse |
title |
Regulation of glycolysis in brown adipocytes by HIF-1α |
title_short |
Regulation of glycolysis in brown adipocytes by HIF-1α |
title_full |
Regulation of glycolysis in brown adipocytes by HIF-1α |
title_fullStr |
Regulation of glycolysis in brown adipocytes by HIF-1α |
title_full_unstemmed |
Regulation of glycolysis in brown adipocytes by HIF-1α |
title_sort |
regulation of glycolysis in brown adipocytes by hif-1α |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2017-06-01 |
description |
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. |
url |
https://doi.org/10.1038/s41598-017-04246-y |
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