Graduate School of Biomedical Sciences, Nagasaki University, Japan.
Biol Pharm Bull. 2011;34(9):1514-7. doi: 10.1248/bpb.34.1514.
We have developed in vivo gene transfer to mesothelial cells on the peritoneal organs, including the stomach. Simple instillation of naked plasmid DNA onto the gastric serosal surface in mice resulted in effective but transient transgene expression. Here, we developed a simple method to improve not only the transfection efficiency but also the duration of transgene expression. Rubbing the gastric serosal surface using a medical spoon immediately after instillation of naked plasmid DNA onto the gastric serosal surface resulted in 59-fold higher transgene expression 24 h after administration in rats. Without rubbing, transgene expression decreased under the detection limit 7 d after administration. On the other hand, rubbing the gastric serosal surface with a medical spoon after instillation of plasmid DNA prolonged transgene expression for one month. Mechanistic study in mice revealed that improved transfection should not be due to stimulation of cell function such as macropinocytosis by rubbing because rubbing before instillation of plasmid DNA did not improve transfection. Plasmid DNA should enter effectively into cells during rubbing. These findings are valuable to develop an effective method of in vivo gene transfer into peritoneal organs.
我们已经开发了一种将基因转移到腹膜器官间皮细胞的体内方法,包括胃。将裸质粒 DNA 简单地滴注到小鼠胃浆膜表面,可导致有效的但短暂的转基因表达。在这里,我们开发了一种简单的方法来提高转染效率和转基因表达的持续时间。在将裸质粒 DNA 滴注到胃浆膜表面后立即用医用勺子摩擦胃浆膜表面,可使大鼠给药后 24 小时的转基因表达提高 59 倍。如果不摩擦,转基因表达在给药后 7 天就会低于检测限。另一方面,在滴注质粒 DNA 后用医用勺子摩擦胃浆膜表面可使转基因表达延长一个月。在小鼠中的机制研究表明,改善转染不应归因于摩擦刺激细胞功能,如胞饮作用,因为在滴注质粒 DNA 之前摩擦并不能改善转染。在摩擦过程中,质粒 DNA 应该有效地进入细胞。这些发现对于开发腹膜器官体内基因转移的有效方法是有价值的。