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作 者:付康[1] 程首超 刘收[1] 陈孝平[1] 陆婕[1] 柳欣[1] 陈正望[1]
机构地区:[1]华中科技大学生命科学与技术学院生物物理与生物化学研究所,武汉430074 [2]湖北省咸宁市中心医院儿科,咸宁437100
出 处:《华中科技大学学报(医学版)》2007年第5期663-666,共4页Acta Medicinae Universitatis Scientiae et Technologiae Huazhong
基 金:国家863计划(No2002AA214061);国家自然科学基金(No30370647;30470823)资助项目
摘 要:目的构建人同种异体移植炎症因子-1(allograft inflammatory factor-1,AIF-1)基因的真核表达载体并在小鼠成纤维细胞系(NIH3T3)中表达,为进一步研究AIF-1蛋白的功能奠定基础。方法利用基因重组技术,构建带有AIF-1基因的2种重组真核表达载体:pcDNA3.1(-)/AIF-1与pEGFP-C1/AIF-1。利用脂质体法将2种重组质粒分别转染NIH3T3细胞,用荧光倒置显微镜及Western blot方法观察及鉴定AIF-1在细胞中的稳定表达及瞬时表达。结果酶切分析及DNA序列测定证实,AIF-1基因片段被分别克隆入真核表达载体pcDNA3.1(-)与pEGFP-C1。荧光显微镜观察到NIH3T3细胞中有绿色荧光分布。Western blot结果表明,转染重组质粒的NIH3T3细胞中,AIF-1表达量明显增高。结论成功构建了2种重组真核表达载体:pcDNA3.1(-)/AIF-1与pEGFP-C1/AIF-1,经转染NIH3T3细胞株获得了AIF-1蛋白的瞬时表达及稳定表达。Objective To construct two recombinant eukaryotic expression vectors of human allograft inflammatory factor-1(AIF-1),and express two recombinant genes in the mouse NIH3T3 cell line respectively,laying a foundation for further study on biological functions of AIF-1.Methods By using gene modification techniques,two recombinant eukaryotic expression vectors of AIF-1 including pcDNA3.1(-)/AIF-1 and pEGFP-C1/AIF-1 were constructed.The recombinant vectors were transfected into NIH3T3 cells by lipofectamine.Stable and transient expression in cells was observed and identified by a fluorescent inverted microscope and Western blot method.Results Restrictive enzyme digestion analysis and DNA sequencing revealed that human AIF-1 gene was cloned into eukaryotic expression vectors pcDNA3.1(-)/AIF-1 and pEGFP-C1/AIF-1 respectively.The fluorescent inverted microscopy showed that green fluorescence was expressed in NIH3T3 cells.NIH3T3 cells transfected by recombinant vectors showed significantly increased expression of AIF-1 by Western blot.Conclusion The two recombinant eukaryotic expression vectors can be successfully constructed.The AIF-1 protein can be stably and transiently expressed in NIH3T3 cells.
关 键 词:同种异体移植因子-1 NIH3T3细胞 转染 基因表达
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