Nead M A, McCance D J
Department of Microbiology and Immunology, University of Rochester, New York 14642, USA.
J Invest Dermatol. 1995 Nov;105(5):668-71. doi: 10.1111/1523-1747.ep12324367.
Human keratinocytes are notoriously difficult to transfect. We have optimized a method for introducing plasmid DNA into keratinocytes that pairs the polycation poly-L-ornithine with a dimethylsulfoxide (DMSO) shock. The optimum poly-L-ornithine conditions for keratinocyte transfection entailed incubating the cells with 12 micrograms/ml poly-L-ornithine and 10 micrograms DNA for 6 h, followed by a 4-min 25% DMSO shock. Based on kinetic studies, 1 h is enough time to produce 10% positive cells in transient transfections, which increases up to an average of 20% after 6 h. Transfected cells survive passaging, and marker plasmids and selection can be used to yield stable transfectants at a rate twofold higher than in cells transfected with polybrene and DMSO. Transient transfection rates were significantly higher using poly-L-ornithine/DMSO than with the polybrene/DMSO or polybrene/glycerol methods previously reported. Overall, transfection mediated by poly-L-ornithine provides an efficient and inexpensive means of transiently or stably introducing DNA into keratinocytes.
众所周知,人类角质形成细胞很难转染。我们优化了一种将质粒DNA导入角质形成细胞的方法,该方法将聚阳离子聚-L-鸟氨酸与二甲基亚砜(DMSO)休克相结合。角质形成细胞转染的最佳聚-L-鸟氨酸条件是将细胞与12微克/毫升聚-L-鸟氨酸和10微克DNA孵育6小时,然后进行4分钟的25% DMSO休克。基于动力学研究,在瞬时转染中,1小时足以产生10%的阳性细胞,6小时后平均增加到20%。转染后的细胞能够传代存活,标记质粒和筛选可用于产生稳定转染子,其效率比用聚凝胺和DMSO转染的细胞高出两倍。使用聚-L-鸟氨酸/DMSO的瞬时转染率明显高于先前报道的聚凝胺/DMSO或聚凝胺/甘油方法。总体而言,聚-L-鸟氨酸介导的转染为将DNA瞬时或稳定导入角质形成细胞提供了一种高效且廉价的方法。