Kogure Kentaro, Akita Hidetaka, Harashima Hideyoshi
Faculty of Pharmaceutical Sciences, Hokkaido University, Kita 12, Nishi 6, Kita-ku, Sapporo City, Hokkaido 060-0812, Japan.
J Control Release. 2007 Oct 8;122(3):246-51. doi: 10.1016/j.jconrel.2007.06.018. Epub 2007 Jun 27.
In this review, a new concept called "Programmed Packaging" is proposed for developing non-viral gene delivery systems. A Multifunctional Envelope-type Nano Device (MEND) was developed based on this concept, which can enter into cells via macropinocytosis and facilitate transfection activities as efficiently as an adenovirus. Intracellular trafficking of MEND was optimized in order to prevent lysosomal degradation and to enhance nuclear translocation. A quantitative analytical method (CIDIQ) was also established to evaluate each step in intracellular trafficking of genes as well as carriers. A comparative study between Lipofectamin and an adenovirus showed that intra-nuclear disposition, which includes the transcriptional process, translational process, etc., can be the limiting step for Lipofectamin PLUS. These studies indicated the importance of controlling intra-nuclear disposition in the development of an efficient non-viral gene delivery system.
在本综述中,提出了一种名为“程序化包装”的新概念,用于开发非病毒基因递送系统。基于这一概念开发了一种多功能包膜型纳米装置(MEND),它可以通过巨胞饮作用进入细胞,并能像腺病毒一样高效地促进转染活性。对MEND的细胞内运输进行了优化,以防止溶酶体降解并增强核转位。还建立了一种定量分析方法(CIDIQ)来评估基因以及载体在细胞内运输的各个步骤。脂质体转染试剂(Lipofectamin)和腺病毒之间的比较研究表明,包括转录过程、翻译过程等在内的核内分布可能是脂质体转染试剂PLUS的限制步骤。这些研究表明,在开发高效非病毒基因递送系统时,控制核内分布非常重要。