Evaluation and Optimization of Lipofectamine 3000 Reagents for Transient Gene Expression in KYSE-30 Esophagus Cancer Cell Line

Reihaneh Alsadat Mahmoudian, M. Farshchian, M. Abbaszadegan
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引用次数: 1

Abstract

Background and Aim: Transfection of DNA/RNA sequence into eukaryotic cells has a major effect on scientific studies. Various methods are used to transfer the DNA/RNA sequence into cells, such as lipid-based carriers as the available and easy procedure. Transfection with cationic lipid liposome is introduced as a simple and efficient procedure for monitoring the DNA/RNA sequence through gene function analysis, including fluorescence imaging RNA and protein expression. This study aimed to investigate the transfection efficiency and cell death through GFP expression in human esophageal squamous cell carcinoma (ESCC) cell line KYSE-30 using Lipofectamine 3000 reagent. Methods: The pCDH-513b plasmid DNA was transfected into KYSE-30 cells using Lipofectamine 3000 in different concentrations of the plasmid DNA and reagent. The transfection efficiency was evaluated by fluorescence microscope and flow cytometry analysis to determine the percentage of GFP-expressing cells. Moreover, the viability and death of transfected KYSE-30 cells were evaluated using a trypan blue exclusion assay. Results: The transfection efficiency of KYSE-30 with Lipofectamine 3000 was increased with higher plasmid DNA concentration and a lower amount of Lipofectamine 3000 reagent. The Optimized concentration of 1.5 µg plasmid DNA and volume of one µl of lipofectamine 3000 reagents were identified for 95% transfection efficiency in the KYSE-30 cell line. The viability and death of transfected cells were 43% and 58% after transfection, respectively. Conclusion: The results indicated that Lipofectamine 3000 might not be suitable for transfection in KYSE-30 cells due to increased cell death. *Corresponding Author: Mohammad Reza Abbaszadegan; Email: abbaszadeganmr@mums.ac.ir Please cite this article as: Mahmoudian RA, Farshchian M, Abbaszadegan MR. Evaluation and Optimization of Lipofectamine 3000 Reagents for Transient Gene Expression in KYSE-30 Esophagus Cancer Cell Line. Arch Med Lab Sci. 2019;5(4):1-9. https://doi.org/10.22037/amls.v5i4.31081
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脂质体3000试剂在食管癌KYSE-30细胞中瞬时基因表达的评价与优化
背景与目的:将DNA/RNA序列转染真核细胞对科学研究具有重要影响。将DNA/RNA序列转移到细胞中有多种方法,例如脂质载体是可用且简单的方法。阳离子脂质体转染是一种简单有效的方法,通过基因功能分析监测DNA/RNA序列,包括荧光成像RNA和蛋白质表达。本实验采用Lipofectamine 3000试剂,研究GFP在人食管鳞癌(ESCC)细胞株KYSE-30中的转染效率和细胞死亡情况。方法:将pCDH-513b质粒DNA以不同浓度的Lipofectamine 3000转染到KYSE-30细胞中。采用荧光显微镜和流式细胞术检测转染效率,测定表达gfp的细胞百分比。此外,使用台盼蓝排斥试验评估转染的KYSE-30细胞的活力和死亡。结果:质粒DNA浓度越高,Lipofectamine 3000试剂用量越少,KYSE-30转染效率越高。在KYSE-30细胞系中,质粒DNA的最佳浓度为1.5µg,脂质体3000试剂的最佳体积为1µl,转染效率为95%。转染后细胞存活率为43%,死亡率为58%。结论:Lipofectamine 3000可能不适合转染KYSE-30细胞,因为它会增加细胞的死亡。*通讯作者:Mohammad Reza Abbaszadegan;Mahmoudian RA, Farshchian M, Abbaszadegan MR. Lipofectamine 3000试剂对食管癌KYSE-30瞬时基因表达的评价与优化。中华医学杂志,2019;5(4):1-9。https://doi.org/10.22037/amls.v5i4.31081
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