Transfection with fluorinated lipoplexes based on fluorinated analogues of DOTMA, DMRIE and DPPES

被引:18
作者
Gaucheron, J [1 ]
Santaella, C [1 ]
Vierling, P [1 ]
机构
[1] Univ Nice, Chim Bioorgan Lab, CNRS, UMR 6001, F-06108 Nice 2, France
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2002年 / 1564卷 / 02期
关键词
gene delivery; synthetic vector; cationic lipid;
D O I
10.1016/S0005-2736(02)00469-8
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
Fluorinated double-chain (poly)cationic lipids (one or both of these chains being ended by a highly fluorinated tail) which are close analogues of DOTMA, DMRIE or DPPES were designed as synthetic vectors for gene delivery. For N/P ratios (N=number of amine functions of the lipid; P= number of DNA phosphates) from 0.8 to 5, these fluorinated cationic lipids condensed DNA, with or without the use of DOPE, to form fluorinated lipoplexes. No specific cell toxicity was evidenced for these new fluorinated lipoplexes. The efficiency of some of the fluorinated lipoplexes to transfect lung epithelial A549 cells was comparable to that of the first generation of fluorinated lipoplexes made from fluorinated analogues of DOGS (Transfectam) [Bioconjug. Chem. 12 (2001) 114]. These results, combined with the higher in vivo transfection potential found for fluorinated lipoplexes than for conventional lipoplexes or PEI polyplexes [J. Gene Med. 3 (2001) 109], confirm that fluorinated lipoplexes are very promising gene transfer systems. (C) 2002 Elsevier Science B.V All rights reserved.
引用
收藏
页码:349 / 358
页数:10
相关论文
共 20 条
[11]  
Miller AD, 1998, ANGEW CHEM INT EDIT, V37, P1769
[12]   Evidence for the role of proteoglycans in cation-mediated gene transfer [J].
Mislick, KA ;
Baldeschwieler, JD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (22) :12349-12354
[13]   Proteoglycans mediate cationic Liposome-DNA complex-based gene delivery in vitro and in vivo [J].
Mounkes, LC ;
Zhong, W ;
Cipres-Palacin, G ;
Heath, TD ;
Debs, RJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (40) :26164-26170
[14]   Virus-sized self-assembling lamellar complexes between plasmid DNA and cationic micelles promote gene transfer [J].
Pitard, B ;
Aguerre, O ;
Airiau, M ;
Lachagès, AM ;
Boukhnikachvili, T ;
Byk, G ;
Dubertret, C ;
Herviou, C ;
Scherman, D ;
Mayaux, JF ;
Crouzet, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (26) :14412-14417
[15]   Polyethylenimine but not cationic lipids promotes transgene delivery to the nucleus in mammalian cells [J].
Pollard, H ;
Remy, JS ;
Loussouarn, G ;
Demolombe, S ;
Behr, JP ;
Escande, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (13) :7507-7511
[16]   Synthesis of highly fluorinated di-O-alk(en)yl-glycerophospholipids and evaluation of their biological tolerance [J].
Ravily, V ;
Gaentzler, S ;
Santaella, C ;
Vierling, P .
HELVETICA CHIMICA ACTA, 1996, 79 (02) :405-425
[17]   Gene transfer with lipospermines and polyethylenimines [J].
Remy, JS ;
Abdallah, B ;
Zanta, MA ;
Boussif, O ;
Behr, JP ;
Demeneix, B .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 30 (1-3) :85-95
[18]   Lipopolycationic telomers for gene transfer: Synthesis and evaluation of their in vitro transfection efficiency [J].
Verderone, G ;
van Craynest, N ;
Boussif, O ;
Santaella, C ;
Bischoff, R ;
Kolbe, HVJ ;
Vierling, P .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (07) :1367-1379
[19]   CELLULAR AND MOLECULAR BARRIERS TO GENE-TRANSFER BY A CATIONIC LIPID [J].
ZABNER, J ;
FASBENDER, AJ ;
MONINGER, T ;
POELLINGER, KA ;
WELSH, MJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (32) :18997-19007
[20]   In vitro gene delivery to hepatocytes with galactosylated polyethylenimine [J].
Zanta, MA ;
Boussif, O ;
Adib, A ;
Behr, JP .
BIOCONJUGATE CHEMISTRY, 1997, 8 (06) :839-844