Batard P, Jordan M, Wurm F
Swiss Federal Institute of Technology Lausanne, Center of Biotechnology CBUE, Department of Chemistry, 1015, Lausanne, Switzerland.
Gene. 2001 May 30;270(1-2):61-8. doi: 10.1016/s0378-1119(01)00467-x.
Using flow cytometry, single cell sorting, confocal microscopy and fluorescent plasmids, a thorough study of DNA uptake, DNA fate and DNA expression in mammalian cells transfected with the widely used calcium-phosphate precipitation method was executed. We show for the first time that up to 100,000 plasmid molecules can be delivered into individual cells, but also that DNA transfer into cells is a dynamic process that follows a defined kinetics of uptake and intracellular processing. Analyses by flow cytometry and confocal microscopy have also supported results suggesting endocytosis during Ca-Pi transfection. We also demonstrate that expression-enhancing treatment with glycerol during transfection did not result in increased DNA uptake. While cells with maximal DNA load appear to express the highest level of the transgene, these cells are negatively impacted in terms of growth and survival.
利用流式细胞术、单细胞分选、共聚焦显微镜和荧光质粒,对采用广泛使用的磷酸钙沉淀法转染的哺乳动物细胞中的DNA摄取、DNA命运和DNA表达进行了全面研究。我们首次表明,多达10万个质粒分子可被递送至单个细胞中,而且DNA转入细胞是一个动态过程,遵循特定的摄取和细胞内加工动力学。流式细胞术和共聚焦显微镜分析也支持了有关钙磷转染过程中存在内吞作用的结果。我们还证明,转染过程中用甘油进行的增强表达处理并未导致DNA摄取增加。虽然具有最大DNA负载量的细胞似乎表达最高水平的转基因,但这些细胞在生长和存活方面受到负面影响。