Intracellular trafficking of nonviral vectors

被引:274
作者
Medina-Kauwe, LK
Xie, J
Hamm-Alvarez, S
机构
[1] Cedars Sinai Med Ctr, Gene Therapeut Res Inst, Los Angeles, CA 90048 USA
[2] Univ Calif Los Angeles, Dept Med, David Geffen Sch Med, Los Angeles, CA USA
[3] Univ So Calif, Dept Pharmaceut Sci, Los Angeles, CA USA
关键词
nonviral; trafficking; vector; cytoskeleton;
D O I
10.1038/sj.gt.3302592
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
Nonviral vectors continue to be attractive alternatives to viruses due to their low toxicity and immunogenicity, lack of pathogenicity, and ease of pharmacologic production. However, nonviral vectors also continue to suffer from relatively low levels of gene transfer compared to viruses, thus the drive to improve these vectors continues. Many studies on vector-cell interactions have reported that nonviral vectors bind and enter cells efficiently, but yield low gene expression, thus directing our attention to the intracellular trafficking of these vectors to understand where the obstacles occur. Here, we will review nonviral vector trafficking pathways, which will be considered here as the steps from cell binding to nuclear delivery. Studies on the intracellular trafficking of nonviral vectors has given us valuable insights into the barriers these vectors must overcome to mediate efficient gene transfer. Importantly, we will highlight the different approaches used by researchers to overcome certain trafficking barriers to gene transfer, many of which incorporate components from biological systems that have naturally evolved the capacity to overcome such obstacles. The tools used to study trafficking pathways will also be discussed.
引用
收藏
页码:1734 / 1751
页数:18
相关论文
共 233 条
[1]   MEMBRANE CONTACT, FUSION, AND HEXAGONAL (HII) TRANSITIONS IN PHOSPHATIDYLETHANOLAMINE LIPOSOMES [J].
ALLEN, TM ;
HONG, K ;
PAPAHADJOPOULOS, D .
BIOCHEMISTRY, 1990, 29 (12) :2976-2985
[2]  
ALLENDE D, 2004, BIOPHYS J, V13, P13
[3]   A role for phosphoinositide 3-kinase in the completion of macropinocytosis and phagocytosis by macrophages [J].
Araki, N ;
Johnson, MT ;
Swanson, JA .
JOURNAL OF CELL BIOLOGY, 1996, 135 (05) :1249-1260
[4]   CHLORATE - A POTENT INHIBITOR OF PROTEIN SULFATION IN INTACT-CELLS [J].
BAEUERLE, PA ;
HUTTNER, WB .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1986, 141 (02) :870-877
[5]   Adenovirus type 7 penton -: Purification of soluble pentamers from Escherichia coli and development of an integrin-dependent gene delivery system [J].
Bal, HP ;
Chroboczek, J ;
Schoehn, G ;
Ruigrok, RWH ;
Dewhurst, S .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2000, 267 (19) :6074-6081
[6]  
Barron L. G., 1999, NONVIRAL VECTORS GEN, P229
[7]   Towards membrane protein design: PH-sensitive topology of histidine-containing polypeptides [J].
Bechinger, B .
JOURNAL OF MOLECULAR BIOLOGY, 1996, 263 (05) :768-775
[8]  
Benmerah A, 1999, J CELL SCI, V112, P1303
[9]   AP-2/Eps15 interaction is required for receptor-mediated endocytosis [J].
Benmerah, A ;
Lamaze, C ;
Bègue, B ;
Schmid, SL ;
Dautry-Varsat, A ;
Cerf-Bensussan, N .
JOURNAL OF CELL BIOLOGY, 1998, 140 (05) :1055-1062
[10]   Isolation of a common receptor for coxsackie B viruses and adenoviruses 2 and 5 [J].
Bergelson, JM ;
Cunningham, JA ;
Droguett, G ;
KurtJones, EA ;
Krithivas, A ;
Hong, JS ;
Horwitz, MS ;
Crowell, RL ;
Finberg, RW .
SCIENCE, 1997, 275 (5304) :1320-1323