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首页> 外文期刊>Life sciences >MiR-199a-3p mediates the adipogenic differentiation of bone marrow-derived mesenchymal stem cells by regulating KDM6A/WNT signaling
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MiR-199a-3p mediates the adipogenic differentiation of bone marrow-derived mesenchymal stem cells by regulating KDM6A/WNT signaling

机译:MiR-199A-3P通过调节KDM6A / WNT信号传导来介导骨髓衍生的间充质干细胞的脂肪切征

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摘要

A number of evidences suggest that microRNAs are involved in the adipogenic commitment of mesenchymal stem cells (MSCs). Recent studies have investigated that miR-199a-3p played a pivotal role in adipocyte differentiation. However, the detailed mechanism in this complex biological process remains largely unknown. In current study, we found that the expression of miR-199a-3p was gradually increased during adipogenic differentiation of bone marrow derived mesenchymal stem cells (BMMSCs). Enhanced expression of miR-199a-3p promoted adipogenesis, whereas silence of miR-199a-3p rescued BMMSCs from adipogenic commitment. For further mechanism exploration, KDM6A was confirmed to be the target of miR-199a-3p and the expression of KDM6A was gradually decreased during adipogenic differentiation of BMMSCs. Furthermore, up-regulation of KDM6A markedly abolished the miR-199a-3p overexpression induced adipogenic augmentation, whereas down-regulation of KDM6A suppressed the adipogenic reduction caused by miR-199a-3p silence. In addition, WNT signaling was also verified to be the downstream of miR-199a-3p/KDM6A to regulate adipogenic differentiation of BMMSCs. Taken together, current results indicate that miR-199a-3p regulate adipogenesis of BMMSCs by targeting KDM6A/WNT signaling, which highlights a new insight for a better understanding of molecular mechanism and stem cell based therapy on osteoporotic diseases.
机译:许多证据表明MicroRNA参与了间充质干细胞(MSCs)的脂肪发生承诺。最近的研究已经调查了MiR-199A-3P在脂肪细胞分化中发挥了枢转作用。然而,这种复杂的生物过程中的详细机制仍然很大程度上是未知的。在目前的研究中,我们发现在骨髓衍生的间充质干细胞(BMMSCs)的脂肪分化期间逐渐增加miR-199A-3P的表达。提高miR-199A-3P的表达促进了脂肪生成,而MiR-199A-3P的沉默救出了BMMSCs免受脂肪造成的承诺。为了进一步的机制探索,证实KDM6A是MIR-199A-3P的靶标,并且在BMMSCs的脂肪切征期间KDM6a的表达逐渐降低。此外,KDM6a的上调显着消除了miR-199A-3P过表达诱导的脂肪植物增强,而KDM6A的下调抑制了MIR-199A-3P沉默引起的脂肪生成还原。此外,还验证了WNT信号传导是MiR-199A-3P / KDM6A的下游,以调节BMMSCs的脂肪生成分化。随着KDM6A / WNT信号传导,目前的结果表明,MIR-199A-3P调节了BMMSCS的脂肪生成,这突出了更好地理解分子机制和基于干细胞基于骨质疏松疾病的治疗的新洞察力。

著录项

  • 来源
    《Life sciences》 |2019年第2019期|共8页
  • 作者单位

    Nanjing Univ Sch Med Nanjing Mil Command Jin Ling Hosp Nanjing Gen Hosp Dept Stomatol Nanjing;

    PLA Army Gen Hosp Dept Stomatol Beijing 100000 Peoples R China;

    Nanjing Univ Sch Med Nanjing Mil Command Jin Ling Hosp Nanjing Gen Hosp Dept Stomatol Nanjing;

    Chongqing Med Univ Dept Endodont Affiliated Stomatol Hosp Chongqing 404100 Peoples R China;

    Nanjing Univ Sch Med Nanjing Mil Command Jin Ling Hosp Nanjing Gen Hosp Dept Stomatol Nanjing;

    Nanjing Univ Sch Med Nanjing Mil Command Jin Ling Hosp Nanjing Gen Hosp Dept Stomatol Nanjing;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医药、卫生;
  • 关键词

    miR-199a-3p; KDM6A; WNT signaling; Adipogenic differentiation;

    机译:mir-199a-3p;kdm6a;wnt信号传导;脂肪发生分化;

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