Cationic liposomes for gene delivery:: Novel cationic lipids and enhancement by proteins and peptides

被引:48
作者
Düzgünes, N
de Ilarduya, CT
Simoes, S
Zhdanov, RI
Konopka, K
de Lima, MCP
机构
[1] Univ Pacific, Sch Dent, Dept Microbiol, San Francisco, CA 94115 USA
[2] Univ Navarra, Dept Pharm & Pharmaceut Technol, Sch Pharm, E-31080 Pamplona, Spain
[3] Univ Coimbra, Ctr Neurosci & Cell Biol, Coimbra, Portugal
[4] Univ Coimbra, Dept Biochem, Coimbra, Portugal
[5] Russian Acad Med Sci, VN Orekhovich Inst Biomed Chem, Moscow 119832, Russia
关键词
D O I
10.2174/0929867033457403
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cationic liposome-DNA complexes, also called "lipoplexes", constitute a potentially viable alternative to viral vectors for the delivery of therapeutic genes. Here we review the mechanisms of lipoplex-mediated gene delivery, the barriers to efficient gene expression, and novel cationic lipids used for transfection. We also describe methods for enhancing gene transfer via the use of proteins, including transferrin, albumin and asialofetuin, and synthetic peptides, including GALA and nuclear localization signal peptides. We underscore the importance of understanding the mechanisms of cytoplasmic and nuclear entry of DNA and its dissociation from lipoplexes. We emphasize that the in vitro transfection activity of new lipoplex constructs should be tested in the presence of high serum concentrations to emulate in vivo conditions.
引用
收藏
页码:1213 / 1220
页数:8
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