染料木黄酮对成骨细胞增殖、分化和凋亡影响的实验研究  被引量:1

Effect of genistein on the proliferation, differentiation and apoptosis of the osteoblasts

在线阅读下载全文

作  者:李斌斌[1] 于世凤[1] 庞淑珍[1] 

机构地区:[1]北京大学口腔医学院口腔病理科,100081

出  处:《中华口腔医学杂志》2005年第3期237-240,共4页Chinese Journal of Stomatology

基  金:国家自然科学基金资助项目(30271412);北京大学211工程口腔医学学科群基金资助项目(KQ0221116)

摘  要:目的研究染料木黄酮对成骨细胞增殖、分化和凋亡的影响,以阐明其对骨形成的作用机制。方法酶消化和组织块相结合培养获得原代成骨细胞,并以成骨肉瘤细胞株UMR106细胞作对照,加入不同浓度的染料木黄酮后,流式细胞仪和噻唑蓝比色法(MTT)检测成骨细胞细胞周期比例的改变以及凋亡情况;生化法检测细胞内碱性磷酸酶含量的改变。结果流式细胞分析和MTT观测结果表明:染料木黄酮促进了原代成骨细胞由G0(G1)期向S期、G2期和M期的移行过渡,从而促进了原代成骨细胞的增殖。染料木黄酮对成骨肉瘤细胞株UMR106细胞周期无影响,但可诱导UMR106细胞凋亡。碱性磷酸酶检测结果表明:染料木黄酮可促进原代成骨细胞的分化。结论染料木黄酮可在一定程度上促进成骨细胞的增殖和分化,诱导成骨肉瘤细胞凋亡。Objective To study the effect of genistein on the proliferation, differentiation and apoptosis of the osteoblasts in vitro. Methods The primary osteoblasts (OBs) were obtained from the rat calvaria and the cell line of osteosarcoma -UMR-106 served as control. The cells in the experiment group were grown in 10% (volume fraction) fetal calf serum ( FCS ) + αMEM + various concentrations of genistein. The control groups were grown in 10% FCS +αMEM. The growth of OBs was assessed by flow cytometry and MTT method. The differentiation of OBs was examined by the alkaline phosphatase(ALP) activity. Results Flow cytometry analysis and MTT showed that genistein could prompt primary OB from stage G_0(G_1) to stage S, G_2 or M. By contrast, genistein had no effect on the cell cycle of UMR-106, but could induce its apoptosis. Additionally, the results of ALP activity showed that genistein stimulated the differentiation of primary OB. Conclusions Genistein can stimulate the proliferation and differentiation of the primary osteoblasts in some degree, and induce the apoptosis of osteosarcoma cells.

关 键 词:染料木黄酮 成骨细胞增殖 分化 实验研究 原代成骨细胞 成骨肉瘤细胞株 细胞周期比例 噻唑蓝比色法 流式细胞分析 流式细胞仪 碱性磷酸酶 瘤细胞凋亡 作用机制 不同浓度 检测结果 骨形成 组织块 酶消化 酶含量 细胞内 生化法 

分 类 号:R780.2[医药卫生—口腔医学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象