Optimization of N2a cell transfection mediated by liposome

    loading  Checking for direct PDF access through Ovid



Cationic liposome-mediated cell transfection is reliable and repeatable. However the transfection efficiency is often low.


To study the optimized methods for gene transfection mediated by liposome into N2a cells (mouse neuroblastma cells).


Using traditional adherent method and improved suspension method, 500 ng recombinant plasmid pcDNA3-GFP carrying green fluorescence protein was transfected into N2a cells in 24-well culture plate, which was mediated by 1.5 μL LipofectamineTM LTX Reagent. The expression of green fluorescent protein was observed by inverted fluorescence microscope, and the transfection efficiencies at different transfection ways were calculated. By using improved suspension transfection method, 500 ng plasmid DNA was transfected with different doses of LipofectamineTM LTX Reagent (1.0, 1.5, 2.0, 2.5 μL). The optimal ratio of liposome and DNA was explored.


The transfection efficiency of suspension transfection method was significantly higher than that of the tranditional adherent method (P < 0.01) when using 1.5 μL liposome/500 ng DNA. The transfection efficiency of the 1.0, 1.5, 2.0, 2.5 μL LipofectamineTM LTX on 500 ng plasmid DNA was respectively (76.60±3.85)%, (80.00±4.17)%, (88.00±5.89)%, (54.96±4.23)%. It showed the 500 ng DNA and 2.0 μL liposome achieve the highest transfection efficiency.

Subject headings:

liposome; transfection; green fluorescent protein


Shanxi Provincial Innovation Foundation for Postgraduate, No. 20133075; Innovation and Entrepreneurship Project of Shanxi Province for Higher Education, No. 2013119; Youth Science and Technology Research Fund of Shanxi Medical University, No. 02201101


Zhao YH, Wang RN, Yang GJ, Lu L. Optimization of N2a cell transfection mediated by liposome. Zhongguo Zuzhi Gongcheng Yanjiu. 2014;18(29):4669-4674.

Related Topics

    loading  Loading Related Articles