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Abstract
The thyroid hormone (TH)-controlled recruitment process of brown adipose tissue (BAT) is not fully understood. Here, we show that long-term treatment of T3, the active form of TH, increases the recruitment of thermogenic capacity in interscapular BAT of male mice through hyperplasia by promoting the TH receptor α-mediated adipocyte progenitor cell proliferation. Our single-cell analysis reveals the heterogeneous nature and hierarchical trajectory within adipocyte progenitor cells of interscapular BAT. Further analyses suggest that T3 facilitates cell state transition from a more stem-like state towards a more committed adipogenic state and promotes cell cycle progression towards a mitotic state in adipocyte progenitor cells, through mechanisms involving the action of Myc on glycolysis. Our findings elucidate the mechanisms underlying the TH action in adipocyte progenitors residing in BAT and provide a framework for better understanding of the TH effects on hyperplastic growth and adaptive thermogenesis in BAT depot at a single-cell level.
Thyroid hormone (TH) action regulates brown adipose tissue thermogenic capacity through incompletely understood mechanisms. Here the authors report that T3, the active form of TH, increases thermogenic capacity via thyroid hormone receptor α-mediated hyperplasia of brown adipose tissue adipocyte progenitor cells.
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1 University of Chinese Academy of Sciences, Chinese Academy of Sciences, and Shanghai Jiao Tong University Affiliated Sixth People’s Hospital, CAS Key Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institute of Nutrition and Health, Shanghai, China (GRID:grid.412528.8) (ISNI:0000 0004 1798 5117)
2 Fudan University, Department of Endocrinology and Metabolism, Zhongshan Hospital, Shanghai, China (GRID:grid.8547.e) (ISNI:0000 0001 0125 2443); Fudan University, Fudan Institute for Metabolic Diseases, Shanghai, China (GRID:grid.8547.e) (ISNI:0000 0001 0125 2443)
3 Chinese Academy of Sciences, Omics Core, Bio-Med Big Data Center, Shanghai Institute of Nutrition and Health, Shanghai, China (GRID:grid.9227.e) (ISNI:0000000119573309)
4 Institute of Experimental Medicine, Laboratory of Molecular Cell Metabolism, Budapest, Hungary (GRID:grid.419012.f) (ISNI:0000 0004 0635 7895)
5 Institute of Experimental Medicine, Laboratory of Integrative Neuroendocrinology, Budapest, Hungary (GRID:grid.419012.f) (ISNI:0000 0004 0635 7895)
6 Shanghai Jiaotong University, Department of Endocrinology and Metabolism, Shanghai General Hospital, School of medicine, Shanghai, China (GRID:grid.16821.3c) (ISNI:0000 0004 0368 8293)
7 Shanghai Jiao Tong University Affiliated Sixth People’s Hospital, Shanghai Diabetes Institute, Shanghai Key Laboratory of Diabetes Mellitus, Shanghai Clinical Centre for Diabetes, Shanghai, China (GRID:grid.412528.8) (ISNI:0000 0004 1798 5117)
8 Chinese Academy of Sciences, The Center for Microbes, Development and Health, Institute Pasteur of Shanghai, Shanghai, China (GRID:grid.9227.e) (ISNI:0000000119573309)
9 University of Chinese Academy of Sciences, Chinese Academy of Sciences, and Shanghai Jiao Tong University Affiliated Sixth People’s Hospital, CAS Key Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institute of Nutrition and Health, Shanghai, China (GRID:grid.412528.8) (ISNI:0000 0004 1798 5117); Innovation Center for Intervention of Chronic Disease and Promotion of Health, Shanghai, China (GRID:grid.412528.8); Ministry of Health, Key Laboratory of Food Safety Risk Assessment, Beijing, China (GRID:grid.453135.5) (ISNI:0000 0004 1769 3691)