Long-term, high level in vivo gene expression after electric pulse-mediated gene transfer into skeletal muscle

被引:152
作者
Mir, LM
Bureau, MF
Rangara, R
Schwartz, BT
Scherman, D
机构
[1] Inst Gustave Roussy, CNRS, UMR 1772, F-94805 Villejuif, France
[2] Rhone Poulenc Rorer Vector Dev Dept, CRVA, CNRS, UMR 133, F-94403 Vitry, France
来源
COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE III-SCIENCES DE LA VIE-LIFE SCIENCES | 1998年 / 321卷 / 11期
关键词
DNA delivery; DNA transfer; electropermeabilization; electroporation; gene therapy; muscle; plasmid; transfection;
D O I
10.1016/S0764-4469(99)80003-1
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Gene delivery to skeletal muscle is a promising strategy for the treatment of muscle disorders and for the local or systemic secretion of therapeutic proteins. However, current DNA delivery technologies have to be improved. We report very efficient luciferase gene transfer into muscle fibres obtained through the delivery of squarewave electric pulses of moderate field strength (100-200 V/cm) and of long duration (20 ms) to muscle previously injected with plasmid DNA. This intramuscular 'electrotransfer' method increases reporter gene expression by more than 100 times. It is noteworthy that this expression remains high and stable for at least 9 months. Moreover, intramuscular electrotransfer strongly decreases the interindividual variability usually observed after plasmid DNA injection into muscle fibres. Therefore, DNA electrotransfer in muscle possesses broad potential applications in gene therapy and for physiological, pharmacological and developmental studies. ((C) Academie des sciences / Elsevier, Paris.)
引用
收藏
页码:893 / 899
页数:7
相关论文
共 28 条
[1]   Gene transfer into muscle by electroporation in vivo [J].
Aihara, H ;
Miyazaki, J .
NATURE BIOTECHNOLOGY, 1998, 16 (09) :867-870
[2]  
Ausubel FM., 1994, Curr. Protoc. Mol. Biol
[3]   LIPOFECTION - A HIGHLY EFFICIENT, LIPID-MEDIATED DNA-TRANSFECTION PROCEDURE [J].
FELGNER, PL ;
GADEK, TR ;
HOLM, M ;
ROMAN, R ;
CHAN, HW ;
WENZ, M ;
NORTHROP, JP ;
RINGOLD, GM ;
DANIELSEN, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (21) :7413-7417
[4]   Enhancement of cytotoxicity by electropermeabilization: an improved method for screening drugs [J].
Gehl, J ;
Skovsgaard, T ;
Mir, LM .
ANTI-CANCER DRUGS, 1998, 9 (04) :319-325
[5]   Novel electrode designs for electrochemotherapy [J].
Gilbert, RA ;
Jaroszeski, MJ ;
Heller, R .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 1997, 1334 (01) :9-14
[6]  
Heller R, 1998, CANCER-AM CANCER SOC, V83, P148, DOI 10.1002/(SICI)1097-0142(19980701)83:1<148::AID-CNCR20>3.0.CO
[7]  
2-W
[8]   In vivo gene electroinjection and expression in rat liver [J].
Heller, R ;
Jaroszeski, M ;
Atkin, A ;
Moradpour, D ;
Gilbert, R ;
Wands, J ;
Nicolau, C .
FEBS LETTERS, 1996, 389 (03) :225-228
[9]  
Lee RJ, 1997, CRIT REV THER DRUG, V14, P173
[10]  
LOGAN JJ, 1995, GENE THER, V2, P38