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Repressor transcription factor 7-like 1 promotes adipogenic competency in precursor cells

机译:阻遏物转录因子7-like 1促进前体细胞的成脂能力

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摘要

The identification of factors that define adipocyte precursor potential has important implications for obesity. Preadipocytes are fibroblastoid cells committed to becoming round lipid-laden adipo-cytes. In vitro, this differentiation process is facilitated by conflu-ency, followed by adipogenic stimuli. During adipogenesis, a large number of cytostructural genes are repressed before adipocyte gene induction. Here we report that the transcriptional repressor transcription factor 7-like 1 (TCF7L1) binds and directly regulates the expression of cell structure genes. Depletion of TCF7L1 inhibits differentiation, because TCF7L1 indirectly induces the adipogenic transcription factor peroxisome proliferator-activated receptor γ in a manner that can be replaced by inhibition of myosin II activity. TCF7L1 is induced by cell contact in adipogenic cell lines, and ectopic expression of TCF7L1 alleviates the conf luency requirement for adi-pocytic differentiation of precursor cells. In contrast, TCF7L1 is not induced during confluency of non-adipogenic fibroblasts, and, remarkably, forced expression of TCF7L1 is sufficient to commit non-adipogenic fibroblasts to an adipogenic fate. These results establish TCF7L1 as a transcriptional hub coordinating cell-cell contact with the transcriptional repression required for adipogenic competency.
机译:鉴定定义脂肪细胞前体潜能的因素对肥胖具有重要意义。前脂肪细胞是成纤维细胞样细胞,致力于变成圆形的载脂脂肪细胞。在体外,通过融合和随后的成脂刺激可促进这种分化过程。在脂肪形成过程中,在诱导脂肪细胞基因之前,大量的细胞结构基因被抑制。在这里我们报告说,转录抑制因子转录因子7样1(TCF7L1)结合并直接调节细胞结构基因的表达。 TCF7L1的耗尽会抑制分化,因为TCF7L1以可以被抑制肌球蛋白II活性替代的方式间接诱导脂肪形成转录因子过氧化物酶体增殖物激活的受体γ。 TCF7L1由成脂细胞系中的细胞接触诱导,TCF7L1的异位表达减轻了前体细胞脂肪分化的融合要求。相反,在非成脂性成纤维细胞汇合期间不会诱导TCF7L1,并且显着地,TCF7L1的强制表达足以使非成脂性成纤维细胞进入成脂命运。这些结果建立了TCF7L1作为协调细胞间接触与成脂能力所需的转录抑制作用的转录中心。

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    Division of Endocrinology, Diabetes, and Metabolism, Departments of Medicine and Genetics and Institute for Diabetes, Obesity, and Metabolism, Perelman School of Medicine at the University of Pennsylvania;

    Division of Endocrinology, Diabetes, and Metabolism, Departments of Medicine and Genetics and Institute for Diabetes, Obesity, and Metabolism, Perelman School of Medicine at the University of Pennsylvania;

    Division of Endocrinology, Diabetes, and Metabolism, Departments of Medicine and Genetics and Institute for Diabetes, Obesity, and Metabolism, Perelman School of Medicine at the University of Pennsylvania;

    Division of Endocrinology, Diabetes, and Metabolism, Departments of Medicine and Genetics and Institute for Diabetes, Obesity, and Metabolism, Perelman School of Medicine at the University of Pennsylvania;

    Department of Bioengineering, University of Pennsylvania, Philadelphia, PA 19104;

    Department of Bioengineering, University of Pennsylvania, Philadelphia, PA 19104;

    Division of Endocrinology, Diabetes, and Metabolism, Departments of Medicine and Genetics and Institute for Diabetes, Obesity, and Metabolism, Perelman School of Medicine at the University of Pennsylvania;

    Division of Endocrinology, Diabetes, and Metabolism, Departments of Medicine and Genetics and Institute for Diabetes, Obesity, and Metabolism, Perelman School of Medicine at the University of Pennsylvania;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 00:41:01

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