Non-Viral Gene Delivery Methods

被引:3
作者
Wang, Weiwei [1 ,2 ,3 ]
Li, Wenzhong [1 ,2 ,3 ]
Ma, Nan [1 ,2 ,3 ]
Steinhoff, Gustav [1 ]
机构
[1] Univ Rostock, Dept Cardiac Surg, Reference & Translat Ctr Cardiac Stem Cell Therap, D-18057 Rostock, Germany
[2] Helmholtz Zentrum Geesthacht, Ctr Biomat Dev, D-14513 Teltow, Germany
[3] Helmholtz Zentrum Geesthacht, Berlin Brandenburg Ctr Regenerat Therapies BCRT, D-14513 Teltow, Germany
关键词
Non-viral gene delivery; gene therapy; physical gene delivery; chemical gene delivery; lipoplex; polyplex; transfection; LOW-MOLECULAR-WEIGHT; IN-VIVO ELECTROPORATION; LIPID-DNA COMPLEXES; HYDRODYNAMICS-BASED TRANSFECTION; BRAIN-BARRIER DISRUPTION; NAKED PLASMID DNA; CATIONIC LIPOSOMES; SKELETAL-MUSCLE; CELL-CYCLE; LIPOFECTION EFFICIENCY;
D O I
暂无
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
Gene delivery has attracted increasing interest as a highly promising therapeutic method to treat various diseases, including both genetic and acquired disorders. Viral-vectors based gene delivery can achieve higher transduction efficiency and long-term gene expression, but they may be associated with some shortcomings, such as immunogenicity, carcinogenicity, poor target cell specificity, inability to transfer large size genes and high costs. Non-viral approaches show high potential due to advantages of relative safety, ability to transfer large size gene, less toxicity and easiness for preparation etc. However, the clinical application of non-viral methods is still restricted by some limitations including low transfection efficiency and poor transgene expression. In order to improve gene transfer efficacy, a lot of efforts have been made in the past years, and numerous gene carriers and techniques have been developed. In this review, we summarized the features, drawbacks and prospects of existing and emerging non-viral gene delivery methods.
引用
收藏
页码:46 / 60
页数:15
相关论文
共 247 条
[71]   Electroporation: theory and methods, perspectives for drug delivery, gene therapy and research [J].
Gehl, J .
ACTA PHYSIOLOGICA SCANDINAVICA, 2003, 177 (04) :437-447
[72]   MODE OF FORMATION AND STRUCTURAL FEATURES OF DNA CATIONIC LIPOSOME COMPLEXES USED FOR TRANSFECTION [J].
GERSHON, H ;
GHIRLANDO, R ;
GUTTMAN, SB ;
MINSKY, A .
BIOCHEMISTRY, 1993, 32 (28) :7143-7151
[73]   Excitation-induced Ca2+ influx and skeletal muscle cell damage [J].
Gissel, H ;
Clausen, T .
ACTA PHYSIOLOGICA SCANDINAVICA, 2001, 171 (03) :327-334
[74]  
Godbey WT, 2000, J BIOMED MATER RES, V51, P321, DOI 10.1002/1097-4636(20000905)51:3<321::AID-JBM5>3.3.CO
[75]  
2-I
[76]   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
[77]   Control by osmotic pressure of voltage-induced permeabilization and gene transfer in mammalian cells [J].
Golzio, M ;
Mora, MP ;
Raynaud, C ;
Delteil, C ;
Teissié, J ;
Rols, MP .
BIOPHYSICAL JOURNAL, 1998, 74 (06) :3015-3022
[78]   The effect of liposome size on the final lipid/DNA ratio of cationic lipoplexes [J].
Gonçalves, E ;
Debs, RJ ;
Heath, TD .
BIOPHYSICAL JOURNAL, 2004, 86 (03) :1554-1563
[79]   High toxicity, low receptor density, and low integration frequency severely impede the use of adenovirus vectors for production of transgenic mice [J].
Gordon, JW .
BIOLOGY OF REPRODUCTION, 2002, 67 (04) :1172-1179
[80]   Efficient gene transfer using reversibly cross-linked low molecular weight polyethylenimine [J].
Gosselin, MA ;
Guo, WJ ;
Lee, RJ .
BIOCONJUGATE CHEMISTRY, 2001, 12 (06) :989-994