文章摘要
杨海1 钱静1 蒋小琴1 舒荣文2 王讯1.miR-188-5p 对肾间质纤维化过程中MMP-13表达的影响*[J].,2014,14(15):2848-2852
miR-188-5p 对肾间质纤维化过程中MMP-13表达的影响*
Effect of miR-188-5p on the Expression of MMP-13 During RenalInterstitial Fibrosis in Mice*
  
DOI:
中文关键词: 肾间质纤维化  基质金属蛋白酶  miR-188-5p
英文关键词: Renal interstitial fibrosis  Matrixmetalloproteinases  miR-188-5p
基金项目:国家自然科学基金项目(31301127)
作者单位
杨海1 钱静1 蒋小琴1 舒荣文2 王讯1 1 解放军一七一医院内三科江西九江3320002 解放军南京军区总院保健科江苏南京210002 
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中文摘要:
      摘要目的:探讨miR-188-5p 对肾间质纤维化过程中基质金属蛋白酶(matrixmetalloproteinases,MMPs)表达的影响。方法:采用 TGF-β1 诱导肾小球系膜细胞(Mesangial cells,MC)纤维化,观察纤维化过程中miR-188-5p 和MMP-13 的表达变化;通过报告基因 实验研究miR-188-5p 对MMP-13 的调控作用;通过脂质体转染的方法将人工合成的miR-188-5p mimics/inhibitor 转入细胞内增 加或减少miR-188-5p 的表达,进一步观察miR-188-5p 对MMP-13 表达的影响。结果:TGF-β1 诱导肾小球系膜细胞纤维化后 miR-188-5p 的表达明显升高,而MMP-13表达下调;报告基因实验表明miR-188-5p 对MMP-13 的表达有明显的调控作用,减少 miR-188-5p 的表达后MMP-13 的表达上调,而增加miR-188-5p 的表达后MMP-13 的表达下调,呈明显负性调控。结论:在肾间质 纤维化过程中,miR-188-5p 可能通过抑制MMP-13 的表达而发挥促纤维化的作用,本研究为肾间质纤维化的治疗提供了新的靶 点。
英文摘要:
      ABSTRACT Objective:To explore the role of miR-188-5p on the expression of matrixmetallo- proteinases 13 (MMPs-13) during renal interstitial fibrosis in mice.Methods: Mice renal mesangial cells (MC) were treated with TGF-β1 at concentration of 2ng/ml for 24h, then the mRNA and protein level of miR-188-5p and MMP-13 were tested. Next, reporter gene experiment was used to verify the effect of miR-188-5p on the regulation of MMP-13. In order to observe the effect on MMP-13, level of miR-188-5p in MC cell were then up/down regulated by mimics/inhibitor through Lipofectamine transfection.Results: TGF-β1 increased the expression of the miR-188-5p, while the mRNA and protein level of MMP-13 were reduced. Reporter gene experiment confirmed the negative regulation of miR-188-5p on MMP-13 expression. Up-regulation of miR-188-5p could inhibit the expression of MMP-13, while down-regulation of miR-188-5p could increade the level of MMP-13. Conclusion:In renal interstitial fibrosis, miR-188-5p may play a fibrogenic role by down-regulating the expression of MMP-13. This study provided a new therapeutic target for renal interstitial fibrosis.
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