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机构地区:[1]中南大学生殖与干细胞工程研究所,湖南长沙410078
出 处:《西北农林科技大学学报(自然科学版)》2010年第12期20-24,共5页Journal of Northwest A&F University(Natural Science Edition)
基 金:国家自然科学基金项目(30570937);国家高技术研究发展计划项目(2006AA02A102);中南大学研究生创新基金项目(2340-74334000003)
摘 要:【目的】对小鼠胚胎干细胞(mESCs)转染条件进行优化。【方法】分别将0.5×105,1×105,2×105,4×105个细胞接种24孔板(各细胞量均接种2孔),培养48h在其细胞融合度分别为30%,50%,70%,90%左右时,分别设置相同的(0.8μgDNA/2μL脂质体)和不同的DNA/脂质体用量(DNA量(μg)/Lipo量(μL)分别为0.4/1,0.8/2,1.6/4,3.2/8),采用脂质体(LipofectamineTM2000)转染法,将pEGFP-N1报告基因载体转染到mESCs中,48h后通过荧光观察和流式分析检测各组EGFP荧光强度,比较转染效率。【结果】在质粒及脂质体用量相同(0.8μgDNA/2.0μL脂质体)的条件下,随着细胞融合度的增加,EGFP荧光强度逐渐减弱,在细胞融合度为30%,50%,70%,90%左右时转染,各组EGFP阳性细胞率分别为56.4%,51.8%,40.8%和23.3%。提高转染质粒及脂质体量可在一定程度上提高转染效率,但脂质体的细胞毒性也随之增加,不利于细胞生长。【结论】低融合度(30%~50%)条件下,使用0.8μgDNA/2.0μL脂质体对mESCs进行转染,可获得较高的转染效率(>50%),同时可维持良好的细胞状态。[Objective] The study was done to optimize the transfection efficiency of mouse embryonic stem cells(mESCs).[Method] mESCs were seeded into 24-well plates at a density of 0.5×10^5,1×10^5,2×10^5,4×10^5 per well(each for two wells).48 h later,cells were transfected when cell confluence was 30%,50%,70%,90% respectively.The reporter plasmid pEGFP-N1 was transfected into cells using Lipofectamine^TM 2000 by using the same amount(0.8 μg DNA/2 μL liposome) or different amounts of DNA and liposome(DNA(μg)/liposome(μL):0.4/1,0.8/2,1.6/4,3.2/8) respectively.48 hr later,the fluorescence intensities in each group were observed and the transfection efficiencies were compared.[Result] The result of fluorescence microscopy and FACS analysis showed that the percentage of EGFP positive cells gradually decreased(56.4%,51.8%,40.8% and 23.3% respectively) as the cell confluence increased(30%,50%,70% and 90% respectively) when using the same amount of DNA and liposome(0.8 μg DNA/2.0 μL liposome/well of 24-well plate).When using more DNA and liposome,transfection efficiency further increased.However,obvious cytotoxicity could be observed.[Conclusion] High transfection efficiency(50%) on mESCs could be achieved by using 0.8 μg DNA/2.0 μL liposome/well of 24-well plate under condition of low cell confluences(30%-50%).
关 键 词:小鼠胚胎干细胞 细胞融合度 脂质体法 PEGFP-N1 转染效率
分 类 号:R321.1[医药卫生—人体解剖和组织胚胎学]
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