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A comparative study on transfection efficiency of green fluorescent protein after concentration of lentivirus by three methods |
BI Ranran1,BAI Rui1,LIU Zhiqiang2,and LIU Huiliang3 |
1.Department of Internal Medicine-Cardiovascular,3.Institute of Cardiology,the Third Medical Centre,Chinese PLA General Hospital,Beijing 100039,China; 2.Institute of Military Cognition and Brain Science,PLA Military Medical Research Institute,Beijing 100850,China |
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Abstract Objective To compare the transfection efficiency of green fluorescent protein (GFP) after concentration of lentivirus by ultrafiltration tube, ultracentrifugation and virusconcentrate. Methods pMD2.G, psPAX2 and GFP vector strains were shaken overnight in a shaker and the three plasmids were extracted with kits.pMD2.G, psPAX2 and GFP vector plasmids were proportionally mixed with transfection reagents and transfected into 293T cells to produce virus.The virus supernatant was collected and concentrated by ultrafiltration tube, ultracentrifugation and virus concentrate. The 293T cells were inoculated into three groups, and the concentrated viral concentrates of 2, 4, 8,16 μl were added into the culture medium of 293T cells inoculated into each group, after 48 hours, the expression of GFP in 293T cells transfected with lentivirus was detected by fluorescence microscopy and flow cytometry. Results The results of fluorescence microscopy showed that the expression rate of GFP increased with the increase of the transfection amount, and the highest expression rate of GFP was obtained when the virus was transfected into 293T cells by ultrafiltration tube. Flow cytometry showed that the expression rates of 2, 4, 8,16 μl GFP in virus concentrate group were (2.4±0.1)%,(3.8±0.3)%,(8.2±0.6)% and(12.2±0.3)% respectively; the expression rates of 2, 4, 8,16 μl GFP in ultrafiltration tube group were (5.4±0.3)%,(7.4±0.4)%,(12.7±0.1)% and (17.3±0.6)% respectively; the expression rates of 2, 4, 8,16 μl GFP in ultracentrifugation group were (0.7±0.1)%,(1.2±0.1)%,(2.1±0.1)% and (0.4±0.2)%, respectively. Compared with the other two groups, the ultrafiltration tube group had significant difference(P<0.05). Conclusion The transfection efficiency of lentiviral GFP is different by different methods. The transfection efficiency of lentiviral GFP by ultrafiltration tube is the highest among the three lentiviral enrichment methods.
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Received: 12 November 2018
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[1] |
孟凡荣,陈 琛,万海粟,等.慢病毒载体及其研究进展[J].中国肺癌杂志, 2014,17(12):870-876.
|
[2] |
傅继凡,陈 健.慢病毒转染大鼠破骨样细胞研究[J].中国老年学, 2016, 36(3):516-519.
|
[3] |
王 鑫, 李彦林, 金耀峰,等. BMP-2、TGF-β_3重组腺病毒载体的构建及其在滇南小耳猪BMSCs中的表达[J]. 中国修复重建外科杂志, 2014,28(7):896-902.
|
[4] |
Zhu C H, Lei W, Chen Z R. Construction of a lentiviral vector encoding heme oxygenase 1 and its introduction into mouse adipose tissue-derived stem cells[J].Genet Mol Res,2015, 14(3):10705-10716.
|
[5] |
Tang Y, Garson K, Li L, et al. Optimization of lentiviral vector production using polyethylenimine-mediated transfection.[J]. Oncol Lett, 2015, 9(1):55-62.
|
[6] |
尹 飚, 杨逸禧, 杨 波,等.红色荧光基因慢病毒转染骨髓间充质干细胞:表达21 d对细胞活性无影响[J]. 中国组织工程研究, 2015, 19(10):1539-1543.
|
[7] |
Sun X , Zeng H , Kumar A , et al. Constitutively expressed IFITM3 protein in human pulmonary endothelial cells poses an early infection block to human influenza viruses[J]. J Virol, 2016, 90(24):11157-11167.
|
[8] |
Pan S, Wan J Z, Liu S S, et al. Lentivirus carrying the Atohl gene infects normal rat cochlea[J]. Neural Regeneration Res, 2013, 8(17):1551-1559.
|
[9] |
谢 柳, 雷水生, 赵元淑,等.NT-3基因过表达慢病毒载体的构建和包装及鉴定[J]. 中风与神经疾病杂志, 2014, 31(8):680-683.
|
[10] |
陈志华, 林素勇, 韩宏景,等.慢病毒转染KISS1基因对人结直肠癌HCT116细胞增殖、侵袭和迁移能力的影响[J].吉林大学学报(医学版), 2017,43(3):577-581.
|
[11] |
周睿卿, 龚玉萍, 林 娟,等. 慢病毒转染脐血CD34+造血干细胞方法的优化[J]. 四川大学学报(医学版), 2013, 44(1):130-134.
|
[12] |
樊守刚, 吴小涛, 王运涛,等. 骨髓间充质干细胞经慢病毒转染绿色荧光蛋白后的体内观察[J]. 东南大学学报(医学版), 2010, 29(2):163-166.
|
[13] |
王艳丽, 张 旭, 戴 娟,等.慢病毒介导绿色荧光蛋白基因转染大鼠软骨细胞表达研究[J]. 现代生物医学进展, 2013, 13(10):1840-1843.
|
[14] |
陈 斌, 倪 勇. 慢病毒转染大鼠骨髓间充质干细胞研究[J]. 中国热带医学, 2009, 9(2):235-236.
|
[15] |
张 徐,钱 晖,朱 伟,等. 慢病毒转染人骨髓间质干细胞研究[J]. 江苏大学学报(医学版), 2008, 18(2):127-130.
|
[16] |
肖 渝,李彦林,王 坤,等. 三种携带GFP慢病毒转染兔骨髓间充质干细胞的效果[J]. 中国组织工程研究, 2017,21(29):56-61.
|
[17] |
管小俊,宋 琳,郭雪君,等.携带绿色荧光蛋白基因慢病毒转染的大鼠骨髓间充质干细胞的干细胞特性检测[J]. 诊断学理论与实践, 2011, 10(6):527-530.
|
[18] |
曹 鎏,李 飞,冯 华.活体干细胞标记与示踪方法研究进展[J]. 人民军医, 2012, 55(10):1004-1006.
|
[19] |
李 潇, 金征宇, 王怡宁,等.报告基因标记在干细胞治疗急性心肌梗死中的应用进展[J]. 中国医学科学院学报, 2015, 37(5):612-617.
|
[20] |
Kurazumi H, Li T S, Takemoto Y, et al. Haemodynamic unloading increases the survival and affects the differentiation of cardiac stem cells after implantation into an infarcted heart[J]. Eur J Cardiothorac Surg, 2014, 45(6):976-982
|
|
|
|