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首页> 外文期刊>Environmental toxicology and pharmacology >Role of miR-199b-5p in regulating angiogenesis in mouse myocardial microvascular endothelial cells through HSF1/VEGF pathway
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Role of miR-199b-5p in regulating angiogenesis in mouse myocardial microvascular endothelial cells through HSF1/VEGF pathway

机译:miR-199b-5p在通过HSF1 / VEGF途径调节小鼠心肌微血管内皮细胞血管生成中的作用

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摘要

Our study explored effects of miR-199b-5p on angiogenesis in mouse myocardial microvascular endothelial cells (MMVECs) and the involved working mechanisms. We applied explant culture to incubate C57/BL6 mouse MMVECs. Lipofection was used to transfect miR-199b-5p mimic, miR-199b-5p inhibitor and miR-199b-5p scramble respectively. MMVECs were divided into miR-199b-5p up-regulation, miR-199b-5p down-regulation and control groups based on above sequence. Expressions of miR-199b-5p, heat shock factor protein 1 (HSF1) mRNA were assessed by real-time quantitative polymerase chain reaction (RT-QPCR). Expressions of HSF1 and vascular endothelial growth factor (VEGF) were assessed by Western Blotting. Cell proliferation was assessed by CCK8. Tubule formation assay was conducted to assess formation of blood vessels. Results showed that miR-199b-5p up/down-regulation groups exhibited no obvious differences in the expressions of HSF1 mRNA compared to control group. However, miR-199b-5p up-regulation group recorded lower expressions of HSF1 and VEGF in the level of protein, and reduced cell proliferation and tubule formation. Whereas, miR-199b-5p down-regulation group presented the contrary results. The experiment indicated that miR-199b-5p can regulate proliferation and angiogenesis in mouse MMVECs through the pathway of HSF1/VEGF.
机译:我们的研究探索了miR-199b-5p对小鼠心​​肌微血管内皮细胞(MMVECs)血管生成的影响及其涉及的工作机制。我们将外植体培养物用于培养C57 / BL6小鼠MMVEC。脂质体转染分别转染miR-199b-5p模拟物,miR-199b-5p抑制剂和miR-199b-5p争夺。根据上述序列,将MMVECs分为miR-199b-5p上调,miR-199b-5p下调和对照组。通过实时定量聚合酶链反应(RT-QPCR)评估miR-199b-5p,热休克因子蛋白1(HSF1)mRNA的表达。通过蛋白质印迹法评估HSF1和血管内皮生长因子(VEGF)的表达。通过CCK8评估细胞增殖。进行小管形成测定以评估血管的形成。结果显示,与对照组相比,miR-199b-5p上调/下调组的HSF1 mRNA表达无明显差异。但是,miR-199b-5p上调组记录了HSF1和VEGF在蛋白质水平上的较低表达,并减少了细胞增殖和小管形成。而miR-199b-5p下调组则得出相反的结果。实验表明,miR-199b-5p可以通过HSF1 / VEGF途径调节小鼠MMVECs的增殖和血管生成。

著录项

  • 来源
    《Environmental toxicology and pharmacology 》 |2016年第10期| 142-148| 共7页
  • 作者单位

    Department of Cardiovascular Medicine, Shanghai East Hospital, Tongji University School of Medicine, Shanghai 200120, China;

    Department of Cardiovascular Medicine, Shanghai East Hospital, Tongji University School of Medicine, Shanghai 200120, China;

    Department of Cardiovascular Medicine, Shanghai East Hospital, Tongji University School of Medicine, Shanghai 200120, China;

    Department of Cardiovascular Medicine, Shanghai East Hospital, Tongji University School of Medicine, Shanghai 200120, China;

    Department of Cardiovascular Medicine, Shanghai East Hospital, Tongji University School of Medicine, Shanghai 200120, China;

    Department of Cardiovascular Medicine, Shanghai East Hospital, Tongji University School of Medicine, Shanghai 200120, China;

    Department of Cardiovascular Medicine, Shanghai East Hospital, Tongji University School of Medicine, Shanghai 200120, China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    miR-199b-5p; Myocardial microvascular endothelial cells; HSF1; VEGF; Angiogenesis;

    机译:miR-199b-5p;心肌微血管内皮细胞;HSF1;VEGF;血管生成;

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