Cost efficient and effective gene transfer into the human natural killer cell line, NK92

被引:26
作者
Grund, EM [1 ]
Muise-Helmericks, RC [1 ]
机构
[1] Med Univ S Carolina, Dept Cell Biol & Anat, Hollings Canc Ctr, Charleston, SC 29425 USA
关键词
electroporation; NK cells; transient expression; RNAi;
D O I
10.1016/j.jim.2004.10.008
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Introducing genes into cells is a crucial step in many fields of basic research, as well as for the development of new drugs and therapies, Many cell types are resistant to normal methods of gene delivery, such as lipid based transfection and electroporation. Delivery to resistant cell lines can be costly or inefficient. Natural killer (NK) cells are highly resistant to transfection. We have developed a novel method to deliver exogenous genes in the NK cell line, NK92. Using a combination of electroporation and a defined buffer, we were able to obtain an electroporation efficiency of 40% in NK92 cells. Using RNAi, we show significant reduction of an endogenous protein (ETS1) using this optimized buffer and electroporation conditions. Taken to.-ether, the results show a functional and cost effective method for the expression of exogenous genes in NK cells. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:31 / 36
页数:6
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