Effects of membrane-active agents in gene delivery

被引:80
作者
Wagner, E
机构
[1] Univ Vienna, Bioctr, Inst Biochem, A-1030 Vienna, Austria
[2] Bender & Co, A-1121 Vienna, Austria
关键词
amphipathic peptides; cytosolic delivery; DNA transfection; endosome destabilization; receptor-mediated gene delivery;
D O I
10.1016/S0168-3659(97)00249-6
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A large variety of membrane-modifying agents have been used for the enhancement of DNA(lipo)polycation complex based gene transfer. The magnitude of improvement depends on the nature of the membrane-modifying agent and the (poly)cationic carrier. Within the lipid-free polymer-based systems (polyfection), ligand-polylysine mediated gene transfer can be improved up to more than 1000-fold by pH-specific endosomolytic peptides, glycerol, bacterial proteins or adenovirus particles. Ligand-polyethylenimine or dendrimer-based systems with per se higher efficiency are only slightly (about ten-fold) enhanced by endosomolytic agents. Membrane-active agents show only minor effects when applied to cationic lipid-based gene transfer (lipofection) with DNA complexes formed under optimized conditions using an three-to four-fold excess of positive charges. Less positively charged lipofection complexes can be strongly improved by the addition of membrane-active peptides. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:155 / 158
页数:4
相关论文
共 40 条
[1]   CONDENSATION OF VECTOR DNA BY THE CHROMOSOMAL PROTEIN HMG1 RESULTS IN EFFICIENT TRANSFECTION [J].
BOTTGER, M ;
VOGEL, F ;
PLATZER, M ;
KIESSLING, U ;
GRADE, K ;
STRAUSS, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 950 (02) :221-228
[2]   A VERSATILE VECTOR FOR GENE AND OLIGONUCLEOTIDE TRANSFER INTO CELLS IN CULTURE AND IN-VIVO - POLYETHYLENIMINE [J].
BOUSSIF, O ;
LEZOUALCH, F ;
ZANTA, MA ;
MERGNY, MD ;
SCHERMAN, D ;
DEMENEIX, B ;
BEHR, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7297-7301
[3]   RECEPTOR-MEDIATED GENE-TRANSFER INTO HUMAN T-LYMPHOCYTES VIA BINDING OF DNA/CD3 ANTIBODY PARTICLES TO THE CD3 T-CELL RECEPTOR COMPLEX [J].
BUSCHLE, M ;
COTTEN, M ;
KIRLAPPOS, H ;
MECHTLER, K ;
SCHAFFNER, G ;
ZAUNER, W ;
BIRNSTIEL, ML ;
WAGNER, E .
HUMAN GENE THERAPY, 1995, 6 (06) :753-761
[4]   Effect of size and serum proteins on transfection efficiency of poly((2-dimethylamino)ethyl methacrylate)-plasmid nanoparticles [J].
Cherng, JY ;
vandeWetering, P ;
Talsma, H ;
Crommelin, DJA ;
Hennink, WE .
PHARMACEUTICAL RESEARCH, 1996, 13 (07) :1038-1042
[5]   TRANSFERRIN POLYCATION-MEDIATED INTRODUCTION OF DNA INTO HUMAN LEUKEMIC-CELLS - STIMULATION BY AGENTS THAT AFFECT THE SURVIVAL OF TRANSFECTED DNA OR MODULATE TRANSFERRIN RECEPTOR LEVELS [J].
COTTEN, M ;
LANGLEROUAULT, F ;
KIRLAPPOS, H ;
WAGNER, E ;
MECHTLER, K ;
ZENKE, M ;
BEUG, H ;
BIRNSTIEL, ML .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (11) :4033-4037
[6]   PSORALEN TREATMENT OF ADENOVIRUS PARTICLES ELIMINATES VIRUS-REPLICATION AND TRANSCRIPTION WHILE MAINTAINING THE ENDOSOMOLYTIC ACTIVITY OF THE VIRUS CAPSID [J].
COTTEN, M ;
SALTIK, M ;
KURSA, M ;
WAGNER, E ;
MAASS, G ;
BIRNSTIEL, ML .
VIROLOGY, 1994, 205 (01) :254-261
[7]   HIGH-EFFICIENCY RECEPTOR-MEDIATED DELIVERY OF SMALL AND LARGE (48 KILOBASE GENE CONSTRUCTS USING THE ENDOSOME-DISRUPTION ACTIVITY OF DEFECTIVE OR CHEMICALLY INACTIVATED ADENOVIRUS PARTICLES [J].
COTTEN, M ;
WAGNER, E ;
ZATLOUKAL, K ;
PHILLIPS, S ;
CURIEL, DT ;
BIRNSTIEL, ML .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (13) :6094-6098
[8]  
COTTEN M, 1993, METHOD ENZYMOL, V217, P618
[9]   HIGH-EFFICIENCY GENE-TRANSFER MEDIATED BY ADENOVIRUS COUPLED TO DNA-POLYLYSINE COMPLEXES [J].
CURIEL, DT ;
WAGNER, E ;
COTTEN, M ;
BIRNSTIEL, ML ;
AGARWAL, S ;
LI, CM ;
LOECHEL, S ;
HU, PC .
HUMAN GENE THERAPY, 1992, 3 (02) :147-154
[10]   EFFICIENT DNA TRANSFECTION OF QUIESCENT MAMMALIAN-CELLS USING POLY-L-ORNITHINE [J].
DONG, YH ;
SKOULTCHI, AI ;
POLLARD, JW .
NUCLEIC ACIDS RESEARCH, 1993, 21 (03) :771-772