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Novel flow cytometric approach for the detection of adipocyte subpopulations during adipogenesis

机译:新型流式细胞仪检测脂肪形成过程中脂肪细胞亚群的方法

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The ability of mesenchymal stromal cells (MSCs) to differentiate into adipocytes provides a cellular model of human origin to study adipogenesis in vitro. One of the major challenges in studying adipogenesis is the lack of tools to identify and monitor the differentiation of various subpopulations within the heterogeneous pool of MSCs. Cluster of differentiation (CD)36 plays an important role in the formation of intracellular lipid droplets, a key characteristic of adipocyte differentiation/maturation. The objective of this study was to develop a reproducible quantitative method to study adipocyte differentiation by comparing two lipophilic dyes [Nile Red (NR) and Bodipy 493/503] in combination with CD36 surface marker staining. We identified a subpopulation of adipose-derived stromal cells that express CD36 at intermediate/high levels and show that combining CD36 cell surface staining with neutral lipid-specific staining allows us to monitor differentiation of adipose-derived stromal cells that express CD36intermediate/high during adipocyte differentiation in vitro. The gradual increase of CD36intermediate/high/NRpositive cells during the 21 day adipogenesis induction period correlated with upregulation of adipogenesis-associated gene expression.
机译:间充质基质细胞(MSCs)分化为脂肪细胞的能力提供了人类起源的细胞模型来研究体外脂肪形成。研究脂肪形成的主要挑战之一是缺乏识别和监测MSCs异质库内各种亚群分化的工具。分化簇(CD)36在细胞内脂质小滴的形成中起重要作用,这是脂肪细胞分化/成熟的关键特征。这项研究的目的是通过比较两种亲脂性染料[尼罗红(NR)和Bodipy 493/503]与CD36表面标记物染色相结合的方法,开发一种可重复的定量方法来研究脂肪细胞的分化。我们鉴定了脂肪基质细胞的亚群,这些脂肪细胞表达中/高水平的CD36,并且表明将CD36细胞表面染色与中性脂质特异性染色相结合使我们能够监测脂肪细胞在脂肪细胞中表达CD36中/高的分化体外分化。在21天成脂诱导期,CD36中间/高/ NR阳性细胞的逐渐增加与成脂相关基因的表达上调相关。

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