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重组pcDNA3.1-hBMP-2转染兔脂肪干细胞体外诱导的成骨分化
引用本文:安荣泽,王兆杰,刘凡凡,齐新文,袁小洪,陈军平,赵俊延,胡小军,杨晋,赵豪. 重组pcDNA3.1-hBMP-2转染兔脂肪干细胞体外诱导的成骨分化[J]. 中国组织工程研究与临床康复, 2011, 15(41): 7601-7606. DOI: 10.3969/j.issn.1673-8225.2011.41.001
作者姓名:安荣泽  王兆杰  刘凡凡  齐新文  袁小洪  陈军平  赵俊延  胡小军  杨晋  赵豪
作者单位:遵义医学院第五附属(珠海)医院,广东省珠海市,519100
基金项目:贵州省省长基金课题"组织工程软骨"资助,珠海市医学重点建设专科基金
摘    要:背景:骨形态发生蛋白2具有很强的诱导干细胞成骨活性。目的:构建人骨形态发生蛋白2基因真核表达载体,探讨其转染脂肪干细胞后的成骨效果。方法:通过噬菌斑原位杂交筛选人混合细胞cDNA文库获得人骨形态发生蛋白2基因,与真核表达载体pcDNA3.1-连接,构建重组质粒pcDNA3.1-hBMP-2。利用脂质体LipofectamineTM2000分别介导人骨形态发生蛋白2基因、EGFP基因转染第4代脂肪干细胞,并经G418进行筛选。结果与结论:酶切鉴定及DNA测序结果证实重组质粒pcDNA3.1-hBMP-2构建成功。经计算脂质体介导的脂肪干细胞瞬时转染率为(18.0±0.42)%,并经过G418筛选后获得了稳定转染的细胞。细胞生长曲线表明转染后对脂肪干细胞生长、增殖无明显影响。ELISA检测发现人骨形态发生蛋白2组的人骨形态发生蛋白2因子表达量均高于EGFP组及未转染组,且能够稳定表达。经人骨形态发生蛋白2基因转染的脂肪干细胞的Ⅰ型胶原含量、碱性磷酸酶活性以及钙结节数目均比EGFP组及未转染组有明显升高。

关 键 词:骨形态发生蛋白2  脂肪源性干细胞  脂质体  转染  骨组织工程

Osteogenic differentiation of rabbit adipose derived stem cells transfected with recombinant pcDNA3.1-hBMP-2 in vitro
An Rong-ze,Wang Zhao-jie,Liu Fan-fan,Qi Xin-wen,Yuan Xiao-hong,Chen Jun-ping,Zhao Jun-yan,Hu Xiao-jun,Yang Jin,Zhao Hao. Osteogenic differentiation of rabbit adipose derived stem cells transfected with recombinant pcDNA3.1-hBMP-2 in vitro[J]. Journal of Clinical Rehabilitative Tissue Engineering Research, 2011, 15(41): 7601-7606. DOI: 10.3969/j.issn.1673-8225.2011.41.001
Authors:An Rong-ze  Wang Zhao-jie  Liu Fan-fan  Qi Xin-wen  Yuan Xiao-hong  Chen Jun-ping  Zhao Jun-yan  Hu Xiao-jun  Yang Jin  Zhao Hao
Affiliation:An Rong-ze,Wang Zhao-jie,Liu Fan-fan,Qi Xin-wen,Yuan Xiao-hong,Chen Jun-ping,Zhao Jun-yan,Hu Xiao-jun,Yang Jin,Zhao Hao Orthopedic Department of the Fifth Affiliated Hospital of Zunyi Medical College,Zhuhai 519100,Guangdong Province,China
Abstract:BACKGROUND:Bone morphogenetic protein 2(BMP-2) shows strong potential to induce osteogenesis of stem cells.OBJECTIVE:To construct an eukaryotic expression vector of human BMP-2(hBMP-2) gene and then to investigate its effect in osteogenic differentiation of human adipose-derived stem cells(ADSCs).METHODS:hBMP-2 gene was obtained by screening human mixed cell cDNA library by plaque in situ hybridization and connected with the eukaryotic expression vector pcDNA3.1.The recombinant plasmid pcDNA3.1-hBMP-2 was i...
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