首页> 外文期刊>International journal of molecular medicine >Expression of microRNA-27a in a rat model of osteonecrosis of the femoral head and its association with TGF-/Smad7 signalling in osteoblasts
【24h】

Expression of microRNA-27a in a rat model of osteonecrosis of the femoral head and its association with TGF-/Smad7 signalling in osteoblasts

机译:MicroRNA-27a在股骨头骨折的大鼠模型中的表达及其与成骨细胞中TGF- / Smad7信号的关系

获取原文
获取原文并翻译 | 示例
           

摘要

The present study assessed whether microRNA (miR)-27a is an influential factor in steroid-induced osteonecrosis of the femoral head (ONFH) and investigated the underlying mechanism of action. The results indicated that serum miR-27a was decreased in a rat model of ONFH compared with that in control rats. It was also observed that increased miR-27a expression promoted osteogenic differentiation and cell proliferation, inhibited caspase-3/9 and B-cell lymphoma-2-associated X protein expression and induced alkaline phosphatase (ALP) activity and bone morphogenetic protein (BMP)-2, runt-related transcription factor (Runx)2 and osteonectin mRNA expression in osteoblastic MC3T3-E1 cells. miR-27a mimics also induced transforming growth factor (TGF)- and Smad7 protein expression in MC3T3-E1 cells. Furthermore, transfection with TGF- expression plasmid was able to enhance the effects of miR-27a mimics on osteoblastic differentiation, cell proliferation, ALP activity, BMP-2, Runx2 and osteonectin mRNA expression, and Smad7 protein expression in the MC3T3-E1 cells. Transfection with a TGF- or Smad7 expression plasmid also enhanced the effects of miR-27a mimics on osteoblastic differentiation, cell proliferation, ALP activity and osteonectin mRNA expression in the MC3T3-E1 cells. Taken together, the results of the present study suggested that the induction of TGF-/Smad7 signaling in osteoblasts may be a potential mechanism by which miR-27a regulates steroid-induced ONFH.
机译:本研究评估了microRNA(miR)-27a是否是类固醇诱导的股骨头骨折(ON​​FH)的影响因素,并研究了潜在的作用机制。结果表明,与对照大鼠相比,在ONFH的大鼠大鼠模型中降低了血清miR-27a。还观察到,增加的miR-27a表达促进了骨质发生分化和细胞增殖,抑制了Caspase-3/9和B细胞淋巴瘤-2-相关X蛋白表达和诱导碱性磷酸酶(ALP)活性和骨形态发生蛋白(BMP) -2,runt相关的转录因子(Runx)2和骨溶素mRNA在骨细胞MC3T3-E1细胞中的表达。 MiR-27A模拟物还诱导MC3T3-E1细胞中的转化生长因子(TGF)和Smad7蛋白表达。此外,用TGF-表达质粒转染,能够增强miR-27a模拟对骨细胞分化,细胞增殖,ALP活性,BMP-2,runx2和骨构C切除素mRNA表达的影响,以及MC3T3-E1细胞中的SMAD7蛋白表达。用TGF或SMAD7表达质粒转染还增强了MIR-27A模拟对MC3T3-E1细胞中骨细胞分化,细胞增殖,ALP活性和骨质细胞MRNA表达的影响。在一起,本研究的结果表明,成骨细胞中TGF-/ Smad7信号传导的诱导可能是miR-27a调节类固醇诱导的ONFH的潜在机制。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号