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单个脂肪组织中白色脂肪细胞的发育和功能异质性。

Developmental and functional heterogeneity of white adipocytes within a single fat depot.

机构信息

Section on Integrative Physiology and Metabolism, Joslin Diabetes Center, Harvard Medical School, Boston, MA, USA

Department of Biomedical Sciences, Heritage College of Osteopathic Medicine, Ohio University, Athens, OH, USA.

出版信息

EMBO J. 2019 Feb 1;38(3). doi: 10.15252/embj.201899291. Epub 2018 Dec 10.

Abstract

Recent studies suggest that, even within a single adipose depot, there may be distinct subpopulations of adipocytes. To investigate this cellular heterogeneity, we have developed multiple conditionally immortalized clonal preadipocyte lines from white adipose tissue of mice. Analysis of these clones reveals at least three white adipocyte subpopulations. These subpopulations have differences in metabolism and differentially respond to inflammatory cytokines, insulin, and growth hormones. These also have distinct gene expression profiles and can be tracked by differential expression of three marker genes: Wilms' tumor 1, transgelin, and myxovirus 1. Lineage tracing analysis with dual-fluorescent reporter mice indicates that these adipocyte subpopulations have differences in gene expression and metabolism that mirror those observed in the clonal cell lines. Furthermore, preadipocytes and adipocytes from these subpopulations differ in their abundance in different fat depots. Thus, white adipose tissue, even in a single depot, is comprised of distinct subpopulations of white adipocytes with different physiological phenotypes. These differences in adipocyte composition may contribute to the differences in metabolic behavior and physiology of different fat depots.

摘要

最近的研究表明,即使在单个脂肪组织中,也可能存在不同的脂肪细胞亚群。为了研究这种细胞异质性,我们从小鼠的白色脂肪组织中开发了多种条件永生化的克隆前体脂肪细胞系。对这些克隆的分析揭示了至少三种白色脂肪细胞亚群。这些亚群在代谢方面存在差异,并对炎性细胞因子、胰岛素和生长激素有不同的反应。它们还具有不同的基因表达谱,并可以通过三种标记基因的差异表达来追踪:Wilms 瘤 1 基因、转胶蛋白和正粘病毒 1 基因。用双荧光报告小鼠进行的谱系追踪分析表明,这些脂肪细胞亚群在基因表达和代谢方面的差异反映了在克隆细胞系中观察到的差异。此外,来自这些亚群的前体脂肪细胞和脂肪细胞在不同脂肪组织中的丰度存在差异。因此,白色脂肪组织,即使在单个脂肪组织中,也由具有不同生理表型的不同白色脂肪细胞亚群组成。脂肪细胞组成的这些差异可能导致不同脂肪组织代谢行为和生理学的差异。

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