Polyamidoamine Dendron-Bearing Lipids as a Nonviral Vector: Influence of Dendron Generation

被引:40
作者
Kono, Kenji [1 ]
Ikeda, Ryuji [1 ]
Tsukamoto, Kota [1 ]
Yuba, Eiji [1 ]
Kojima, Chie [1 ]
Harada, Atsushi [1 ]
机构
[1] Osaka Prefecture Univ, Grad Sch Engn, Dept Appl Chem, Sakai, Osaka 5998531, Japan
关键词
MEDIATED GENE-TRANSFER; TRANSFECTION EFFICIENCY; CATIONIC LIPIDS; STEM-CELLS; DELIVERY; DENDRIMERS; DNA; OLIGONUCLEOTIDE; POLYPLEXES; COMPLEXES;
D O I
10.1021/bc200368b
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Recently, we demonstrated that octadecyl chains are important as alkyl chain moieties of polyamidoamine (PAMAM) dendron-bearing lipids for their serum-resistant transfection activity [Bioconjugate Chem. 2007, 18, 1349-1354]. Toward production of highly potent vectors, we examined the influence of the generation of dendron moiety on transfection activity of PAMAM dendron-bearing lipids having two octadecyl chains. We synthesized dendron-bearing lipids with PAMAM G1, G2, and G3 dendrons, designated respectively as DL-G1-2C(18), DL-G2-2C(18), and DL-G3-2C(18). The DL-G2-2C(18) and DL-G3-2C(18) interacted with plasmid DNA effectively and formed stable lipoplexes with small sizes and spherical shape. However, DL-G1-2C(18) interacted with plasmid DNA less effectively and formed tubular-shaped lipoplexes with lower stability and larger size. Cells took up DL-G2-2C(18) and DL-G3-2C(18) lipoplexes efficiently, but cellular uptake of the DL-GI-2C(18) lipoplexes was less efficient. Nevertheless, DL-G1-2C(18) lipoplexes achieved 100-10 000 times higher levels of transgene expression, which was evaluated using luciferase gene as a reporter gene. Confocal scanning laser microscopic analysis of intracellular behaviors of the lipoplexes revealed that DL-G1-2C(18) lipoplexes generated free plasmid DNA molecules in the cytosol more effectively than other lipoplexes did. Moderate binding ability of DL-G1-2C(18) might be responsible for generation of lipoplexes which deliver plasmid DNA into cells, liberate it in the cytoplasm, and induce efficient transgene expression.
引用
收藏
页码:871 / 879
页数:9
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