Lee Migi, Chea Kathleen, Pyda Rajyalakshmi, Chua Melissa, Dominguez Isabel
Department of Medicine, Boston University School of Medicine, Boston, Massachusetts 02118, USA.
J Biomol Tech. 2017 Jul;28(2):67-74. doi: 10.7171/jbt.17-2802-003. Epub 2017 Apr 29.
Mouse embryonic fibroblast (MEF) cells are an important model for developmental biology, disease, and reprogramming studies. However, as with other primary cells, they are challenging to transfect. Although viral gene-delivery methods achieve high gene-delivery efficiency, challenges with cell mutagenesis and safety among others have led to the use and improvement of non-viral gene-delivery methods in MEF cells. Despite the importance of gene delivery in MEF cells, there is limited comparison of method/reagent efficacy. In this study, we compared the effectiveness of different gene-delivery methods and several reagents currently available in MEF cells by introducing a plasmid containing enhanced green fluorescent protein (EGFP). We analyze transfection efficiency by EGFP fluorescence. Our results suggest that two gene-delivery methods-electroporation and magnetofection in combination with a lipid reagent, are the most efficient transfection methods in MEF cells. This study provides a foundation for the selection of transfection methods or reagents when using MEF cells.
小鼠胚胎成纤维细胞(MEF)是发育生物学、疾病和重编程研究的重要模型。然而,与其他原代细胞一样,它们的转染具有挑战性。尽管病毒基因递送方法可实现较高的基因递送效率,但细胞诱变和安全性等挑战促使人们在MEF细胞中使用并改进非病毒基因递送方法。尽管基因递送在MEF细胞中很重要,但方法/试剂功效的比较有限。在本研究中,我们通过导入含有增强型绿色荧光蛋白(EGFP)的质粒,比较了MEF细胞中不同基因递送方法和几种现有试剂的有效性。我们通过EGFP荧光分析转染效率。我们的结果表明,两种基因递送方法——电穿孔法和与脂质试剂结合的磁转染法,是MEF细胞中最有效的转染方法。本研究为使用MEF细胞时选择转染方法或试剂提供了依据。