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芒果苷对缺氧损伤骨髓间充质干细胞凋亡的保护
作者姓名:李晓峰  罗世兴  赵劲民  程建文  谭 桢
作者单位:1广西医科大学第一附属医院创伤骨科手外科,广西壮族自治区南宁市 530021 2广西医科大学第九附属医院暨北海市人民医院骨科,广西壮族自治区北海市 536000
基金项目:广西卫生厅中医药科技专项(GZKZ 10-011)*;广西研究生教育创新项目(2010105981002D26)*;高等学校博士学科点专项科研基金资助项目(20104503110002)*;广西科技厅人口健康与食品安全关键技术研究开发项目(桂科攻 1140003A-31)*;广西卫生厅自筹经费科研课题(Z2012059)*;广西教育厅立项项目(桂教201010LX050)*
摘    要:背景:缺氧性死亡限制了细胞移植和组织再生中细胞的应用。 目的:观察芒果苷对氯化钴作用下骨髓间充质干细胞缺氧损伤性凋亡的保护作用。 方法:体外培养大鼠骨髓间充质干细胞,应用氯化钴建立细胞缺氧模型,以芒果苷对缺氧损伤下的骨髓间充质干细胞进行保护,通过MTT实验观察芒果苷对大鼠骨髓间充质干细胞缺氧损伤的保护作用;采用流式细胞仪检测芒果苷对大鼠骨髓间充质干细胞缺氧保护的细胞凋亡及线粒体膜电位检测结果。 结果与结论:氯化钴能显著抑制大鼠骨髓间充质干细胞的生长,并且呈明显的剂量依赖关系。氯化钴200 μmol/L处理细胞12 h,诱导细胞凋亡率为(42.49±3.96)%;处理细胞24 h,诱导细胞凋亡率为(46.37±4.49)%,随着芒果苷浓度的增加,大鼠骨髓间充质干细胞缺氧损伤的凋亡率逐步减少(P < 0.01),芒果苷对大鼠骨髓间充质干细胞缺氧损伤具有保护作用,且呈浓度依赖性。结果提示,氯化钴缺氧模型能成功诱导大鼠骨髓间充质干细胞凋亡,具有剂量准确可控、无特殊设备要求、易操作等优点;芒果苷能有效抑制缺氧损伤时骨髓间充质干细胞的凋亡,对细胞具有保护作用。中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程全文链接:

关 键 词:干细胞  骨髓干细胞  骨髓间充质干细胞  缺氧  凋亡  芒果苷  氯化钴  省级基金  干细胞图片文章  

Mangiferin protects bone marrow-derived mesenchymal stem cells against hypoxia-induced apoptosis
Authors:Li Xiao-feng  Luo Shi-xing  Zhao Jin-min  Cheng Jian-wen  Tan Zhen
Institution:1Department of Traumatic Orthopaedics and Hand Surgery, First Affiliated Hospital of Guangxi Medical University, Nanning  530021, Guangxi Zhuang Autonomous Region, China
2Department of Orthopedics, Ninth Hospital (Beihai People’s Hospital), Guangxi Medical University, Nanning  536000, Guangxi Zhuang Autonomous Region, China
Abstract:BACKGROUND:Hypoxic death limits application of cells in transplantation and tissue regeneration. OBJECTIVE:To investigate the protective effects of mangiferin on bone marrow-derived mesenchymal stem cells against hypoxia injury-induced apoptosis resulted from cobalt chloride. METHODS:Rat bone marrow-derived mesenchymal stem cells were in vitro cultured and hypoxia cell model was established by cobalt chloride. Model cells were treated with mangiferin. Protective effects of mangiferin were detected using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; cell apoptosis and mitochondrial membrane potential were detected using flow cytometry.   RESULTS AND CONCLUSION:Cobalt chloride significantly inhibited growth of bone marrow-derived mesenchymal stem cells in a dose-dependent manner. The apoptosis rate of cells was (42.49±3.96)% after treated with 200 μmol/L cobalt chloride for 12 hours, (46.37±4.49)% after treated for 24 hours. With increasing concentration of mangiferin, apoptosis of bone marrow-derived mesenchymal stem cells in hypoxic model was gradually reduced (P < 0.01), indicating that mangiferin has a protective effect in a concentration-dependent manner on rat bone marrow-derived mesenchymal stem cells in hypoxic injury. Cobalt chloride can induce hypoxic model successfully in bone marrow-derived mesenchymal stem cells. There are some advantages of accurate dose control, no special equipment requirements, and easy operation. Mangiferin can effectively inhibit bone marrow-derived mesenchymal stem cells apoptosis under hypoxic injury.
Keywords:stem cells  mesenchymal stem cells  hypoxia  apoptosis  membrane potentials  mitochondria  
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