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Distinct properties of adipose stem cell subpopulations determine fat depot-specific characteristics

Title
Distinct properties of adipose stem cell subpopulations determine fat depot-specific characteristics
Author(s)
Nahmgoong, HahnJeon, Yong GeunPark, Eun SeoHa Choi, YoonHan, Sang MunPark, JeuJi, YulSohn, Jee HyungHan, Ji SeulKim, Ye YoungHwang, InjaeLee, Yun KyungHuh, Jin YoungChoe, Sung SikOh, Tae JungChoi, Sung HeeKim, Jong KyoungKim, Jae Bum
Issued Date
2022-03
Citation
Cell Metabolism, v.34, no.3, pp.458 - 472
Type
Article
Author Keywords
single-cell RNA-seqadipose stem cellsfat depotsadipose tissue remodelingobesityadipogenesisinflammationfibrosisbeige adipocyteslymph nodes
Keywords
ADIPOCYTE PRECURSOR CELLSINSULIN-RESISTANCEBEIGE ADIPOCYTESTISSUEADIPOGENESISBROWNLINEAGEOBESITYIDENTIFICATIONPROGENITORS
ISSN
1550-4131
Abstract
In mammals, white adipose tissues are largely divided into visceral epididymal adipose tissue (EAT) and subcutaneous inguinal adipose tissue (IAT) with distinct metabolic properties. Although emerging evidence suggests that subpopulations of adipose stem cells (ASCs) would be important to explain fat depot differences, ASCs of two fat depots have not been comparatively investigated. Here, we characterized heterogeneous ASCs and examined the effects of intrinsic and tissue micro-environmental factors on distinct ASC features. We demonstrated that ASC subpopulations in EAT and IAT exhibited different molecular features with three adipogenic stages. ASC transplantation experiments revealed that intrinsic ASC features primarily determined their adipogenic potential. Upon obesogenic stimuli, EAT-specific SDC1+ ASCs promoted fibrotic remodeling, whereas IAT-specific CXCL14+ ASCs suppressed macrophage infiltration. Moreover, IAT-specific BST2high ASCs exhibited a high potential to become beige adipocytes. Collectively, our data broaden the understanding of ASCs with new insights into the origin of white fat depot differences. © 2021 Elsevier Inc.
URI
http://hdl.handle.net/20.500.11750/17203
DOI
10.1016/j.cmet.2021.11.014
Publisher
Cell Press
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Department of New Biology Laboratory of Single-Cell Genomics 1. Journal Articles

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