M2 macrophages independently promote beige adipogenesis via blocking adipocyte Ets1

Adipose tissue macrophages can promote beige adipose thermogenesis by altering local sympathetic activity. Here, we perform sympathectomy in mice and further eradicate subcutaneous adipose macrophages and discover that these macrophages have a direct beige-promoting function that is independent of s...

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Veröffentlicht in:Nature communications 2024-02, Vol.15 (1), p.1646-1646, Article 1646
Hauptverfasser: Wu, Suyang, Qiu, Chen, Ni, Jiahao, Guo, Wenli, Song, Jiyuan, Yang, Xingyin, Sun, Yulin, Chen, Yanjun, Zhu, Yunxia, Chang, Xiaoai, Sun, Peng, Wang, Chunxia, Li, Kai, Han, Xiao
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Sprache:eng
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Zusammenfassung:Adipose tissue macrophages can promote beige adipose thermogenesis by altering local sympathetic activity. Here, we perform sympathectomy in mice and further eradicate subcutaneous adipose macrophages and discover that these macrophages have a direct beige-promoting function that is independent of sympathetic system. We further identify adipocyte Ets1 as a vital mediator in this process. The anti-inflammatory M2 macrophages suppress Ets1 expression in adipocytes, transcriptionally activate mitochondrial biogenesis, as well as suppress mitochondrial clearance, thereby increasing the mitochondrial numbers and promoting the beiging process. Male adipocyte Ets1 knock-in mice are completely cold intolerant, whereas male mice lacking Ets1 in adipocytes show enhanced energy expenditure and are resistant to metabolic disorders caused by high-fat-diet. Our findings elucidate a direct communication between M2 macrophages and adipocytes, and uncover a function for Ets1 in responding to macrophages and negatively governing mitochondrial content and beige adipocyte formation. Adipose beiging is a positive biological change, which is often thought to be primarily sympathetically induced. Here, the authors show that M2 macrophages can independently promote beige adipogenesis, further revealing the adipocyte transcription factor Ets1 as a negative regulator of this process.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-024-45899-4