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作 者:赵东海[1] 杨淑艳[1] 钟秀宏[1] 张以忠[1] 赵丽薇[1]
机构地区:[1]吉林医药学院病理学教研室,吉林吉林132013
出 处:《山东医药》2012年第11期22-24,共3页Shandong Medical Journal
基 金:吉林省教育厅"十一五"科学技术研究项目资助(2009309)
摘 要:目的体外获得表达重组大鼠GATA4-pEGFP基因的骨髓间充质干细胞(MSCs),为进一步研究后者在心肌梗死治疗中的作用奠定基础。方法提取胎鼠心肌细胞总RNA,RT-PCR法扩增获得GATA4基因,将目的基因克隆到pEGFP-N3载体并获得重组后GATA4-pEGFP质粒,采用密度梯度离心法联合贴壁法分离骨髓单个核细胞并获得MSCs。将重组质粒GATA4-pEGFP以Lipo2000转染到大鼠MSCs,G418筛选2周,Western blot和荧光检测重组质粒在MSCs中的表达情况。结果成功构建重组大鼠GATA4-pEGFP真核表达载体并转染入MSCs中,Western blot和荧光检测证实GATA4-pEGFP基因在MSCs中呈阳性表达。结论成功建立表达大鼠GATA4-pEGFP基因的MSCs,此为利用组织工程学方法治疗心肌梗死的研究奠定了基础。Objective To screen bone marrow mesenchymal stem cells(MSCs) expressing GATA4-pEGFP in vitro,so as to provide theoretical foundation for the research of myocardial infarction.Methods Total RNA was extracted from embryonic myocardial cells,GATA4 gene was amplified by RT-PCR,the target gene was cloned to pEGFP-N3 vector to get recombinant GATA4-pEGFP plasmid,the bone marrow mononuclear cells was derived and MSCs were obtained by gradient centrifugation.The recombinant plasmid was transfected into MSCs using lipofectamine 2000,then screened for 2 weeks by G418,Western blot and immunofluroscence staining were used to examine the expression pattern of transfected protein.Results Recombinant rat GATA4-Pegfp eukaryocyte expression vector was constructed and transfected into MSCs successfully,Western blot and immunofluroscence staining showed that GATA4-Pegfp gene expressed positively in the MSCs.Conclusion MSCs expressing GATA4-pEGFP can be constructed successfully,this provides opportunity to study and treat myocardial infarction using tissue engineering technologies.
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