한빛사논문
Hahn Nahmgoong1,5, Yong Geun Jeon1,5, Eun Seo Park2,5, 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 Kim2,4,*, Jae Bum Kim1,6,*
1National Creative Research Initiatives Center for Adipocyte Structure and Function, Institute of Molecular Biology and Genetics, School of Biological Sciences, Seoul National University, Seoul 08826, Republic of Korea
2Department of New Biology, DGIST, Daegu 42988, Republic of Korea
3Internal Medicine, Seoul National University College of Medicine & Seoul National University Bundang Hospital, Seoul 03080, Republic of Korea
4Present address: Department of Life Sciences, Pohang University of Science and Technology, Pohang 37673, Republic of Korea
5These authors contributed equally
6Lead contact
*Corresponding author
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.
Keywords : single-cell RNA-seq, adipose stem cells, fat depots, adipose tissue remodeling, obesity, adipogenesis, inflammation, fibrosis, beige adipocytes, lymph nodes
논문정보
관련 링크
연구자 키워드
관련분야 연구자보기
관련분야 논문보기