| Literature DB >> 35021043 |
Hahn Nahmgoong1, Yong Geun Jeon1, Eun Seo Park2, Yoon Ha Choi2, Sang Mun Han1, Jeu Park1, Yul Ji1, Jee Hyung Sohn1, Ji Seul Han1, Ye Young Kim1, Injae Hwang1, Yun Kyung Lee3, Jin Young Huh1, Sung Sik Choe1, Tae Jung Oh3, Sung Hee Choi3, Jong Kyoung Kim4, Jae Bum Kim5.
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.Entities:
Keywords: adipogenesis; adipose stem cells; adipose tissue remodeling; beige adipocytes; fat depots; fibrosis; inflammation; lymph nodes; obesity; single-cell RNA-seq
Mesh:
Year: 2022 PMID: 35021043 DOI: 10.1016/j.cmet.2021.11.014
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287