碱性成纤维细胞生长因子真核表达载体的构建及表达  被引量:5

CONSTRUCTION AND EXPRESSION OF BASIC FIBROBLAST GROWTH FACTOR MAMMALIAN EXPRESSION VECTOR

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作  者:张启旭[1] 周刚[1] 陆佳韵[2] 刘芝华[2] 

机构地区:[1]中国医学科学院中国协和医科大学整形外科医院,北京100041 [2]中国医学科学院中国协和医科大学肿瘤研究所分子肿瘤学国家重点实验室

出  处:《中国修复重建外科杂志》2004年第5期435-439,共5页Chinese Journal of Reparative and Reconstructive Surgery

基  金:中国医学科学院重点研究基金资助项目 (971 0 1 9)~~

摘  要:目的 构建人碱性成纤维细胞生长因子 ( basic fibroblast growth factor,b FGF)真核表达质粒 ,研究其在体内外的表达。 方法 通过基因克隆技术 ,构建并大量制备 pc DNA3.1/ myc- His( - ) C- b FGF真核表达体系 ,RT-PCR和细胞免疫组织化学方法检测体外瞬时表达情况 ;直流电脉冲介导重组质粒 pc DNA3.1/ myc- His( - ) C- b FGF和p CD2 -血管内皮细胞生长因子1 2 1 ( vascular endothelial growth factor,VEGF1 2 1 )在兔颈部肌肉瓣内转移并表达 ,测定其促血管生成的生物学效应。 结果 构建的 pc DNA3.1/ myc- His( - ) C- b FGF真核表达体系成功转染体外培养 He L a细胞 ,目的基因在 m RNA水平和蛋白水平均有表达。 pc DNA3.1/ myc- His( - ) C- b FGF和 p CD2 - VEGF1 2 1 重组质粒分别转染在体肌瓣 ,获得外源基因高水平表达。转基因肌肉发生血管增生、血流增强的生物学效应。 结论 构建了人 b FGF真核表达质粒 ,并可在体内外顺利表达 。Objective To construct a mammalian expression vector of basic fibroblast growth factor (bFGF) and to investigate the expression of bFGF in vitro and in vivo. Methods A mammalian expression vector pcDNA3.1/myc His( )C bFGF was constructed with gene cloning technique. The mammalian expression system was prepared and purified. The expression of bFGF cDNA in cultured transfected cells was examined by RT PCR and cell immunohistochemistry. The recombinant plasmids, pcDNA3.1/myc His( )C bFGF and pCD2 VEGF 121 , were transferred into rabbit cervical muscle by direct injection of plasmid following electric pulses in vivo. The transferred gene expression and the biological effect were measured by use of histochemistry and immunohistochemistry analysis. Results The eukaryon expression system pcDNA3.1/myc His( )C bFGF could express the target protein bFGF in vitro. The recombinant plasmids, pcDNA3.1/myc His( )C bFGF and pCD2 VEGF 121 were transferred into muscles flap in vivo successfully. The active proteins bFGF and VEGF 121 were expressed at high levels. Blood vessels increased significantly in the muscles, and blood circulation was improved by local angiogenesis. Conclusion The eukaryon expression vector of bFGF is constructed and can be expressed successfully in vitro and in vivo. That is a primary preparation for the research on tissue transplantation and tissue engineering with bFGF gene therapy.

关 键 词:FGF 真核表达体系 PCDNA3 CD2 体内 人碱性成纤维细胞生长因子 VEGF 目的基因 MRNA水平 重组质粒 

分 类 号:R346[医药卫生—基础医学]

 

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