Nonviral gene transfer to skeletal, smooth, and cardiac muscle in living animals

被引:54
作者
Dean, DA [1 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Div Pulm & Crit Care Med, Chicago, IL 60611 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2005年 / 289卷 / 02期
关键词
electroporation; liposomes; plasmids; transfection; gene expression;
D O I
10.1152/ajpcell.00613.2004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
The study of muscle physiology has undergone many changes over the past 25 years and has moved from purely physiological studies to those intimately intertwined with molecular and cell biological questions. To ask these questions, it is necessary to be able to transfer genetic reagents to cells both in culture and, ultimately, in living animals. Over the past 10 years, a number of different chemical and physical approaches have been developed to transfect living skeletal, smooth, and cardiac muscle systems with varying success and efficiency. This review provides a survey of these methods and describes some more recent developments in the field of in vivo gene transfer to these various muscle types. Both gene delivery for overexpression of desired gene products and delivery of nucleic acids for downregulation of specific genes and their products are discussed to aid the physiologist, cell biologist, and molecular biologist in their studies on whole animal biology.
引用
收藏
页码:C233 / C245
页数:13
相关论文
共 136 条
[1]
ACSADI G, 1991, NEW BIOL, V3, P71
[2]
Gene transfer into muscle by electroporation in vivo [J].
Aihara, H ;
Miyazaki, J .
NATURE BIOTECHNOLOGY, 1998, 16 (09) :867-870
[3]
DNA electrotransfer:: its principles and an updated review of its therapeutic applications [J].
André, F ;
Mir, LM .
GENE THERAPY, 2004, 11 (Suppl 1) :S33-S42
[4]
In vivo transfer efficiency of antisense oligonucleotides into the myocardium using HVJ-liposome method [J].
Aoki, M ;
Morishita, R ;
Higaki, J ;
Moriguchi, A ;
Kida, I ;
Hayashi, S ;
Matsushita, H ;
Kaneda, Y ;
Ogihara, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 231 (03) :540-545
[5]
Optimization of nonviral gene transfer of vascular smooth muscle cells in vitro and in vivo [J].
Armeanu, S ;
Pelisek, J ;
Krausz, E ;
Fuchs, A ;
Groth, D ;
Curth, R ;
Keil, O ;
Quilici, J ;
Rolland, PH ;
Reszka, R ;
Nikol, S .
MOLECULAR THERAPY, 2000, 1 (04) :366-375
[6]
Ausubel F M, 1999, SHORT PROTOCOLS MOL
[7]
Increased gene expression and inflammatory cell infiltration caused by electroporation are both important for improving the efficacy of DNA vaccines [J].
Babiuk, S ;
Baca-Estrada, ME ;
Foldvari, M ;
Middleton, DM ;
Rabussay, D ;
Widera, G ;
Babiuk, LA .
JOURNAL OF BIOTECHNOLOGY, 2004, 110 (01) :1-10
[8]
Muscle electrotransfer as a tool for studying muscle fiber-specific and nerve-dependent activity of promoters [J].
Bertrand, A ;
Ngô-Muller, V ;
Hentzen, D ;
Concordet, JP ;
Daegelen, D ;
Tuil, D .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2003, 285 (05) :C1071-C1081
[9]
Electroporation in combination with a plasmid vector containing SV40 enhancer elements results in increased and persistent gene expression in mouse muscle [J].
Blomberg, P ;
Eskandarpour, M ;
Xia, S ;
Sylvén, C ;
Islam, KB .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 298 (04) :505-510
[10]
Highly effective non-viral gene transfer into vascular smooth muscle cells of cultured resistance arteries demonstrated by genetic inhibition of sphingosine-1-phosphate-induced vasoconstriction [J].
Bolz, SS ;
Pohl, U .
JOURNAL OF VASCULAR RESEARCH, 2003, 40 (04) :399-405