| Literature DB >> 33116305 |
Wenfei Sun1, Hua Dong2, Miroslav Balaz2, Michal Slyper3, Eugene Drokhlyansky3, Georgia Colleluori4, Antonio Giordano4, Zuzana Kovanicova5, Patrik Stefanicka6, Lucia Balazova2, Lianggong Ding2, Anna Sofie Husted7, Gottfried Rudofsky8, Jozef Ukropec5, Saverio Cinti4, Thue W Schwartz7, Aviv Regev9,10,11, Christian Wolfrum12.
Abstract
Adipose tissue is usually classified on the basis of its function as white, brown or beige (brite)1. It is an important regulator of systemic metabolism, as shown by the fact that dysfunctional adipose tissue in obesity leads to a variety of secondary metabolic complications2,3. In addition, adipose tissue functions as a signalling hub that regulates systemic metabolism through paracrine and endocrine signals4. Here we use single-nucleus RNA-sequencing (snRNA-seq) analysis in mice and humans to characterize adipocyte heterogeneity. We identify a rare subpopulation of adipocytes in mice that increases in abundance at higher temperatures, and we show that this subpopulation regulates the activity of neighbouring adipocytes through acetate-mediated modulation of their thermogenic capacity. Human adipose tissue contains higher numbers of cells of this subpopulation, which could explain the lower thermogenic activity of human compared to mouse adipose tissue and suggests that targeting this pathway could be used to restore thermogenic activity.Entities:
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Year: 2020 PMID: 33116305 DOI: 10.1038/s41586-020-2856-x
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962