Polycation liposome-mediated gene transfer in vivo

被引:60
作者
Matsuura, M
Yamazaki, Y
Sugiyama, M
Kondo, M
Ori, H
Nango, M
Oku, N
机构
[1] Univ Shizuoka, Sch Pharmaceut Sci, Dept Med Biochem, Shizuoka 4228526, Japan
[2] Nagoya Inst Technol, Dept Appl Chem, Nagoya, Aichi 466, Japan
[3] Univ Shizuoka, Sch Pharmaceut Sci, COE Program 21st Century, Shizuoka 4228526, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2003年 / 1612卷 / 02期
基金
日本学术振兴会;
关键词
gene transfer; transfection; liposome; polycation; polyethylenimine;
D O I
10.1016/S0005-2736(03)00109-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The polycation liposome (PCL), a recently developed gene transfer system, is simply prepared by a modification of liposomes with cetylated polyethylenitnine (PEI), and shows remarkable transgene efficiency with low cytotoxicity. In the present study, we investigated the applicability of PCLs for in vivo gene transfer, since the PCL-mediated transgene efficiency was found to be maintained in the presence of serum. PCLs composed of dioleoylphosphatidylethanolamine (DOPE) with 5 mol% cetyl PEI (PEI average mr. wt. 1800), were superior for transfection to those of dipalmitoylphosphatidylcholine (DPPC) and cholesterol (2:1 as molar ratio) with 5 inol% cetyl PEI in vitro, although the latter PCLs were more efficient for gene transfer in vivo. PCL-DNA complexes were injected into mice via a tail or the portal vein, with the DNA being a plasmid encoding green fluorescent protein (GFP) or luciferase; and the expression was monitored qualitatively or quantitatively, respectively. Tail vein injection resulted in high expression of both GFP and luciferase genes in lung, and portal vein injection resulted in high expression of both genes in the liver. Concerning the gene delivery efficiency, the PCL was found to be superior to PEI or cetyl PEI alone. The optimal conditions for in vivo transfection with PCLs were also examined. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:136 / 143
页数:8
相关论文
共 47 条
[1]
A powerful nonviral vector for in vivo gene transfer into the adult mammalian brain: Polyethylenimine [J].
Abdallah, B ;
Hassan, A ;
Benoist, C ;
Goula, D ;
Behr, JP ;
Demeneix, BA .
HUMAN GENE THERAPY, 1996, 7 (16) :1947-1954
[2]
Anderson WF, 1998, NATURE, V392, P25
[3]
Polyethylenimine-mediated gene transfer into pancreatic tumor dissemination in the murine peritoneal cavity [J].
Aoki, K ;
Furuhata, S ;
Hatanaka, K ;
Maeda, M ;
Remy, JS ;
Behr, JP ;
Terada, M ;
Yoshida, T .
GENE THERAPY, 2001, 8 (07) :508-514
[4]
Clark PR, 1999, CURR OPIN MOL THER, V1, P158
[5]
Efficient gene transfer by transferrin lipoplexes in the presence of serum [J].
de Ilarduya, CT ;
Düzgünes, N .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2000, 1463 (02) :333-342
[6]
Mannose polyethylenimine conjugates for targeted DNA delivery into dendritic cells [J].
Diebold, SS ;
Kursa, P ;
Wagner, E ;
Cotten, M ;
Zenke, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (27) :19087-19094
[7]
ExGen 500 is an efficient vector for gene delivery to lung epithelial cells in vitro and in vivo [J].
Ferrari, S ;
Moro, E ;
Pettenazzo, A ;
Behr, JP ;
Zacchello, F ;
Scarpa, M .
GENE THERAPY, 1997, 4 (10) :1100-1106
[8]
Protective copolymers for nonviral gene vectors: synthesis, vector characterization and application in gene delivery [J].
Finsinger, D ;
Remy, JS ;
Erbacher, P ;
Koch, C ;
Plank, C .
GENE THERAPY, 2000, 7 (14) :1183-1192
[9]
A versatile system for receptor-mediated gene delivery permits increased entry of DNA into target cells, enhanced delivery to the nucleus and elevated rates of transgene expression [J].
Fisher, KD ;
Ulbrich, K ;
Subr, V ;
Ward, CM ;
Mautner, V ;
Blakey, D ;
Seymour, LW .
GENE THERAPY, 2000, 7 (15) :1337-1343
[10]
Tracking the intracellular path of poly(ethylenimine)/DNA complexes for gene delivery [J].
Godbey, WT ;
Wu, KK ;
Mikos, AG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (09) :5177-5181