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2017
- doi: 10.1038/s41467-017-00182-7
- issn: 2041-1723
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info:eu-repo/semantics/altIdentifier/doi/10.1038/s41467-017-00182-7
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info:eu-repo/semantics/altIdentifier/pmid/28733645
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info:eu-repo/semantics/altIdentifier/eissn/2041-1723
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info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_910F88CBC37F6
info:eu-repo/semantics/openAccess , CC BY 4.0 , https://creativecommons.org/licenses/by/4.0/
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Fat tissue Body fat tissues Adipose tissue Fatty tissueCiter ce document
A. Ferrari et al., « HDAC3 is a molecular brake of the metabolic switch supporting white adipose tissue browning. », Serveur académique Lausannois, ID : 10.1038/s41467-017-00182-7
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White adipose tissue (WAT) can undergo a phenotypic switch, known as browning, in response to environmental stimuli such as cold. Post-translational modifications of histones have been shown to regulate cellular energy metabolism, but their role in white adipose tissue physiology remains incompletely understood. Here we show that histone deacetylase 3 (HDAC3) regulates WAT metabolism and function. Selective ablation of Hdac3 in fat switches the metabolic signature of WAT by activating a futile cycle of de novo fatty acid synthesis and β-oxidation that potentiates WAT oxidative capacity and ultimately supports browning. Specific ablation of Hdac3 in adipose tissue increases acetylation of enhancers in Pparg and Ucp1 genes, and of putative regulatory regions of the Ppara gene. Our results unveil HDAC3 as a regulator of WAT physiology, which acts as a molecular brake that inhibits fatty acid metabolism and WAT browning.Histone deacetylases, such as HDAC3, have been shown to alter cellular metabolism in various tissues. Here the authors show that HDAC3 regulates WAT metabolism by activating a futile cycle of fatty acid synthesis and oxidation, which supports WAT browning.