期刊论文详细信息
eLife
Adipocyte NR1D1 dictates adipose tissue expansion during obesity
David A Bechtold1  Rebecca C Northeast1  Antony D Adamson1  Nichola J Barron1  Peter S Cunningham1  Andrew SI Loudon1  Ann Louise Hunter1  Charlotte E Pelekanou1  Magdalena Grudzien1  Polly Downton1  Jean-Noel Billaud2  Mudassar Iqbal3  Leanne Hodson4  Thomas Cornfield4  David W Ray4  Richard D Unwin5 
[1] Centre for Biological Timing, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom;Digital Insights, Qiagen, Redwood City, United States;Division of Informatics, Imaging and Data Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom;Oxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, and NIHR Oxford Biomedical Research Centre, John Radcliffe Hospital, Oxford, United Kingdom;Stoller Biomarker Discovery Centre, Division of Cancer Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom;
关键词: circadian clock;    energy metabolism;    obesity;    adipose;    Rev-erb-alpha;    Rev-erbα;    Mouse;   
DOI  :  10.7554/eLife.63324
来源: eLife Sciences Publications, Ltd
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【 摘 要 】

The circadian clock component NR1D1 (REVERBα) is considered a dominant regulator of lipid metabolism, with global Nr1d1 deletion driving dysregulation of white adipose tissue (WAT) lipogenesis and obesity. However, a similar phenotype is not observed under adipocyte-selective deletion (Nr1d1Flox2-6:AdipoqCre), and transcriptional profiling demonstrates that, under basal conditions, direct targets of NR1D1 regulation are limited, and include the circadian clock and collagen dynamics. Under high-fat diet (HFD) feeding, Nr1d1Flox2-6:AdipoqCre mice do manifest profound obesity, yet without the accompanying WAT inflammation and fibrosis exhibited by controls. Integration of the WAT NR1D1 cistrome with differential gene expression reveals broad control of metabolic processes by NR1D1 which is unmasked in the obese state. Adipocyte NR1D1 does not drive an anticipatory daily rhythm in WAT lipogenesis, but rather modulates WAT activity in response to alterations in metabolic state. Importantly, NR1D1 action in adipocytes is critical to the development of obesity-related WAT pathology and insulin resistance.

【 授权许可】

CC BY   

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