Nucleofection as an efficient nonviral transfection method for human monocytic cells

被引:48
|
作者
Martinet, W [1 ]
Schrijvers, DM
Kockx, MM
机构
[1] Univ Antwerp, Div Pharmacol, Wilrijk, Belgium
[2] Gen Hosp Middelheim, Dept Pathol, Antwerp, Belgium
关键词
electroporation; gene transfer; green fluorescent protein; monocytic cells; nucleofection;
D O I
10.1023/A:1024157508492
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Despite some progress in the field of gene transfer into hard-to-transfect cells, so far an efficient nonviral method for monocytes has not been available. A comparison of plasmid DNA with capped and polyadenylated mRNA for enhanced green fluorescent protein gene delivery into the commonly used monocytic cell lines U937 and THP-1 suggested that limited DNA trafficking may be the underlying cause of poor transfection results. As Nucleofector technology delivers DNA ( or mRNA) straight into the nucleus, we obtained nucleofection efficiencies of up to 80% without significant cell toxicity. Moreover, as the DNA quickly reaches the nucleus, nucleofected cells were ready for analysis after only 2 - 6 h. The technique is suitable not only for monocytes but also for other hard-to-transfect cells.
引用
收藏
页码:1025 / 1029
页数:5
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