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Genetic and functional characterization of clonally derived adult human brown adipocytes
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute. University of California, USA.
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2015 (English)In: Nature Medicine, ISSN 1078-8956, E-ISSN 1546-170X, Vol. 21, no 4, 389-+ p.Article in journal (Refereed) Published
Abstract [en]

Brown adipose tissue (BAT) acts in mammals as a natural defense system against hypothermia, and its activation to a state of increased energy expenditure is believed to protect against the development of obesity. Even though the existence of BAT in adult humans has been widely appreciated(1-8), its cellular origin and molecular identity remain elusive largely because of high cellular heterogeneity within various adipose tissue depots. To understand the nature of adult human brown adipocytes at single cell resolution, we isolated clonally derived adipocytes from stromal vascular fractions of adult human BAT from two individuals and globally analyzed their molecular signatures. We used RNA sequencing followed by unbiased genome-wide expression analyses and found that a population of uncoupling protein 1 (UCP1)-positive human adipocytes possessed molecular signatures resembling those of a recruitable form of thermogenic adipocytes (that is, beige adipocytes). In addition, we identified molecular markers that were highly enriched in UCP1-positive human adipocytes, a set that included potassium channel K3 (KCNK3) and mitochondrial tumor suppressor 1 (MTUS1). Further, we functionally characterized these two markers using a loss-of-function approach and found that KCNK3 and MTUS1 were required for beige adipocyte differentiation and thermogenic function. The results of this study present new opportunities for human BAT research, such as facilitating cell-based disease modeling and unbiased screens for thermogenic regulators.

Place, publisher, year, edition, pages
2015. Vol. 21, no 4, 389-+ p.
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Biological Sciences Basic Medicine
URN: urn:nbn:se:su:diva-116982DOI: 10.1038/nm.3819ISI: 000352493600021PubMedID: 25774848OAI: diva2:812101


Available from: 2015-05-15 Created: 2015-05-05 Last updated: 2015-05-15Bibliographically approved

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Luijten, Ineke H. N.Nedergaard, Jan
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