首页 | 本学科首页   官方微博 | 高级检索  
     

茶多酚EGCG对人骨髓基质干细胞成骨分化基因表达的影响
引用本文:谢丽华,陈可,李生强,邱龙龙,葛继荣. 茶多酚EGCG对人骨髓基质干细胞成骨分化基因表达的影响[J]. 中医药导报, 2012, 18(6): 3-5,8
作者姓名:谢丽华  陈可  李生强  邱龙龙  葛继荣
作者单位:福建省中医药研究院,福建,福州,350003
基金项目:国家自然科学基金,福建省科技厅公益类科研院所自主选题
摘    要:目的:观察茶多酚EGCG对人骨髓基质干细胞成骨分化基因ALK、COL1A1、RUNX2、BMP-2表达的影响.方法:培养人骨髓基质干细胞,用浓度为10-5M、10-6M茶多酚EGCG以及空白对照组分别作用人骨髓基质干细胞21 d后,采用荧光定量PCR的方法检测成骨相关基因ALK、COL1A1、RUNX2、BMP-2的表达变化.结果:BMP-2基因的表达水平为:10-5M茶多酚组>10-6M茶多酚组>DMSO对照组;ALK、RUNX2、COL1A1基因在茶多酚EGCG组与空白对照组之间表达无明显变化.结论:茶多酚EGCG可以提高人骨髓基质干细胞BMP-2基因的表达水平,有可能是茶多酚促进人骨髓基质干细胞成骨分化的重要基因.

关 键 词:茶多酚  人骨髓间充质干细胞  成骨分化  表没食子儿茶素-3-没食子酸  核心结合因子-2

Effects of tea polyphenols EGCG on the mRNA expression in the osteogenic differentiation of human bone marrow stromal cells
Xie Lihua , Chen Ke , Li Shengqiang , Qiu Longlong , Ge Jirong. Effects of tea polyphenols EGCG on the mRNA expression in the osteogenic differentiation of human bone marrow stromal cells[J]. GUIDING JOURNAL OF TCM, 2012, 18(6): 3-5,8
Authors:Xie Lihua    Chen Ke    Li Shengqiang    Qiu Longlong    Ge Jirong
Affiliation:(Corresponding author)(Fujian Institute of Traditional Chinese Medicine,Fuzhou Fujian 350003)
Abstract:Objective: To study the effects of tea polyphenols EGCG on osteogenic differentiation of human bone marrow stromal cells by testing the mRNA expression level.Methods: HBMSCs were cultured in vitro.HBMSCs were treated with 10-5mol/L、10-6mol/L tea polyphenols and blank group for 21 days.The relative expression of osteogenic gene ALK、COL1A1、RUNX2、BMP-2 were detected by real-time PCR with SYBR Green I.Results: The BMP-2 mRNA expression level:10-5M tea polyphenols group>10-6M tea polyphenols group>blank group.There was no significant difference in the expression of osteogenic gene ALK、COL1A1、RUNX2.Conclusion:Tea polyphenols EGCG could increase the BMP-2 mRNA expression.It could be the important gene that tea polyphenols enhances osteogenesis in the hBMSCs.
Keywords:Tea polyphenols  Human bone marrow stromal cells  Osteogenic Differentiation  EGCG  BMP-2
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号