补肾活血方调控 microRNA-210促进 BMSCs 成骨分化的研究
The kidney-tonifying and blood circulation-promoting recipes promote the osteogenic differentiation of bone mesenehymal stem cells by regulating microRNA-210
投稿时间:2013-05-14  
DOI:
中文关键词:  骨髓间充质干细胞  miR-210  补肾活血
英文关键词:Bone mesenehymal stem cells  miR-210  Kidney-tonifying and blood circulation-promoting recipes
基金项目:
作者单位E-mail
张倍源 陕西省友谊医院,西安,710068 zchuanren@sohu.com 
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中文摘要:
      目的:研究补肾活血方促进骨髓间充质干细胞(Bone Mesenehymal Stem Cells ,BMSCs)成骨分化的分子机制。方法贴壁培养法分离纯化大鼠BMSCs,将培养成功的BMSCs分为空白组、成骨诱导组和中药组,培养7d、14d行矿化结节茜素红染色(Alizarin Red S,ARS),倒置显微镜观察矿化骨结节形成情况,采用real-time PCR检测miR-210的表达变化。结果与空白组比较,成骨诱导组和中药组BMSCs钙化结节数量明显增多,差异有非常显著的统计学意义( P<0.01)。在成骨诱导剂、补肾活血方水提液的作用下,与空白组比较,miR-210表达明显降低,且中药组较成骨诱导组更明显降低miR-210表达。结论补肾活血方通过降低miR-210表达促进BMSCs成骨分化。
英文摘要:
      Objective To investigate the mechanism of osteogenic differentiation of bone mesenehymal stem cells ( BMSCs) promoted by the kidney-tonifying and blood circulation-promoting recipes.Methods BMSCs of SD rats were isolated with adherent separation method and primarily cultured in vitro.Then BMSCs were divided into blank group, osteo-induced group, and Chinese medicine group.At the 7 th day and the 14 th day, the mineralized nodules were stained using Alizarin red statining ( ARS) . The formation of mineralized nodules was observed using a converted microscope.The expression of miR-210 was detected using real-time PCR.Results Compared with that in blank group, the number of mineralized nodules in osteo-induced group and Chinese medicine group increased significantly ( P <0.01 ) .After the intervention of osteogenic inducer and extraction of the kidney-tonifying and blood circulation-promoting recipes, the expression of miR-210 in both groups decreased significantly compared with that in blank group.And the expression in Chinese medicine group was much lower than that in osteo-induced group. Conclusion The kidney-tonifying and blood circulation-promoting recipes can promote the osteogenic differentiation of BMSCs by down-regulating the expression of miRNA-210.
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