[抗炎黄酮类黄素对成骨前细胞MC3T3-E1细胞成骨的影响]。

X. Bing, H. Tao, H. Xin
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引用次数: 0

摘要

目的探讨黄酮类菊花素对成骨前细胞MC3T3-E1成骨的影响。方法在评价金菊素毒性作用后,用DMEM制备成骨前细胞MC3T3-E1细胞悬液,分别用0、25 μmol/L的金菊素培养。采用实时荧光定量PCR检测Runx2、ColA1、OCN等成骨细胞的表达情况。采用SPSS17.0软件包进行统计分析。结果25 μmol/L黄菊花素对成骨前细胞MC3T3-E1无毒性作用。与25 μmol/L chrysin共培养后,Runx2、ColA1和OCN分别在第7天、第14天和第21天表达量最高。结论25 μmol/L黄菊花素可促进成骨前细胞MC3T3-E1成骨基因的表达。
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[Effect of anti-inflammatory flavonoid chrysin on osteogenesis of preosteoblast MC3T3-E1 cells].
PURPOSE To investigation the effect of flavonoid chrysin on osteogenesis of preosteoblast MC3T3-E1 cells. METHODS After evaluation of the toxic effect of chrysin, preosteoblast MC3T3-E1 cell suspension was prepared with DMEM and then the cells were cultured with 0 and 25 μmol/L chrysin. Real-time quantitative PCR was used to detect the expression of osteogenic marlcers including Runx2, ColA1 and OCN. Statistical analysis was performed using SPSS17.0 software package. RESULTS 25 μmol/L chrysin had no toxic effect on preosteoblast MC3T3-E1 cells. After co-culture with 25 μmol/L chrysin,the expression of Runx2, ColA1 and OCN was highest at the 7th,14th and 21th day,respectively. CONCLUSIONS 25 μmol/L chrysin can promote osteogenic gene expression of preosteoblast MC3T3-E1 cell.
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