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snRNA-seq reveals a subpopulation of adipocytes that regulates thermogenesis
- Source :
- Cell Metab
- Publication Year :
- 2020
- Publisher :
- Springer Science and Business Media LLC, 2020.
-
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.
- Subjects :
- Adult
Male
0301 basic medicine
genetic processes
Paracrine Communication
Regulator
Adipose tissue
Cell Separation
Acetates
Biology
Aldehyde Dehydrogenase 1 Family
Article
Mice
Young Adult
03 medical and health sciences
chemistry.chemical_compound
Paracrine signalling
0302 clinical medicine
Adipose Tissue, Brown
Single-cell analysis
Adipocyte
Adipocytes
Animals
Humans
RNA-Seq
Aged
Cell Nucleus
Multidisciplinary
Retinal Dehydrogenase
Cytochrome P-450 CYP2E1
Thermogenesis
Middle Aged
Cell biology
030104 developmental biology
chemistry
Female
Single-Cell Analysis
Energy Metabolism
030217 neurology & neurosurgery
Function (biology)
Subjects
Details
- ISSN :
- 14764687 and 00280836
- Volume :
- 587
- Database :
- OpenAIRE
- Journal :
- Nature
- Accession number :
- edsair.doi.dedup.....04d0e829fb1d588b5e9be24e980e95e0