Mechanism of plasmid delivery by hydrodynamic tail vein injection.: I.: Hepatocyte uptake of various molecules

被引:78
作者
Sebestyen, Magdolna G.
Budker, Vladimir G.
Budker, Tatiana
Subbotin, Vladimir M.
Zhang, Guofeng
Monahan, Sean D.
Lewis, David L.
Wong, So C.
Hagstrom, James E.
Wolff, Jon A.
机构
[1] Univ Wisconsin, Waisman Ctr 355, Dept Pediat, Madison, WI 53705 USA
[2] Univ Wisconsin, Waisman Ctr 355, Dept Med Genet, Madison, WI 53705 USA
[3] Mirus Bio Corp, Madison, WI 53719 USA
关键词
naked DNA; hydrodynamic delivery; mechanism; pores; vesicles; liver; hepatocyte; gene transfer;
D O I
10.1002/jgm.921
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background The hydrodynamic tail vein (HTV) injection of naked plasmid DNA is a simple yet effective in vivo gene delivery method into hepatocytes. It is increasingly being used as a research tool to elucidate mechanisms of gene expression and the role of genes and their cognate proteins in the pathogenesis of disease in animal models. A greater understanding of its mechanism will aid these efforts and has relevance to macromolecular and nucleic acid delivery in general. Methods In an attempt to explore how naked DNA enters hepatocytes the fate of a variety of molecules and particles was followed over a 24-h time frame using fluorescence microscopy. The uptake of some of these compounds was correlated with marker gene expression from a co-injected plasmid DNA. In addition, the uptake of the injected compounds was correlated with the histologic appearance of hepatocytes. Results Out of the large number of nucleic acids, peptides, proteins, inert polymers and small molecules that we tested, most were efficiently delivered into hepatocytes independently of their size and charge. Even T7 phage and highly charged DNA/protein complexes of 60-100 nm in size were able to enter the cytoplasm. In animals co-injected with an enhanced yellow fluorescent protein (EYFP) expression vector and fluorescently labeled immunoglobulin (IgG) hepatocytes flooded with large amounts of IgG, appeared permanently damaged and did not express EYFP-Nuc. Hepatocytes expressing EYFP had only slight IgG uptake. In contrast, when an EYFP expression vector was co-injected with a fluorescently labeled 200-bp linear DNA fragment, both were mostly (in 91% of the observed cells) co-localized to the same hepatocytes 24 h later. Conclusions The appearance of permanently damaged cells with increased uptake of some molecules such as endogenous IgG raised the possibility that a molecule could be present in a hepatocyte but its transport would not be indicative of the transport process that can lead to foreign gene expression. The HTV procedure enables the uptake of a variety of molecules (as previous studies also found), but the uptake process for some of these molecules may be associated with a more disruptive process to the hepatocytes that is not compatible with successful gene delivery. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:852 / 873
页数:22
相关论文
共 46 条
[1]   Hydrodynamics-based transfection of the liver: entrance into hepatocytes of DNA that causes expression takes place very early after injection [J].
Andrianaivo, F ;
Lecocq, M ;
De Coninck, SW ;
Wattiaux, R ;
Jadot, M .
JOURNAL OF GENE MEDICINE, 2004, 6 (08) :877-883
[2]   Liver-targeted gene therapy by SV40-based vectors using the hydrodynamic injection method [J].
Arad, U ;
Zeira, E ;
Abd El-Latif, M ;
Mukherjee, S ;
Mitchell, L ;
Pappo, O ;
Galun, E ;
Oppenheim, A .
HUMAN GENE THERAPY, 2005, 16 (03) :361-371
[3]   Increased hepatic transduction with reduced systemic dissemination and proinflammatory cytokines following hydrodynamic injection of helper-dependent adenoviral vectors [J].
Brunetti-Pierri, N ;
Palmer, DJ ;
Mane, V ;
Finegold, M ;
Beaudet, AL ;
Ng, P .
MOLECULAR THERAPY, 2005, 12 (01) :99-106
[4]   The efficient expression of intravascularly delivered DNA in rat muscle [J].
Budker, V ;
Zhang, G ;
Danko, I ;
Williams, P ;
Wolff, J .
GENE THERAPY, 1998, 5 (02) :272-276
[5]  
Budker V, 1996, GENE THER, V3, P593
[6]  
Budker V, 2000, J GENE MED, V2, P76, DOI 10.1002/(SICI)1521-2254(200003/04)2:2<76::AID-JGM97>3.0.CO
[7]  
2-4
[8]  
BUDKER V, 2006, J GENE MED, V8
[9]   Prolonged liver-specific transgene expression by a non-primate lentiviral vector [J].
Condiotti, R ;
Curran, MA ;
Nolan, GP ;
Giladi, H ;
Ketzinel-Gilad, M ;
Gross, E ;
Galun, E .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 320 (03) :998-1006
[10]   Hydrodynamic liver gene transfer mechanism involves transient sinusoidal blood stasis and massive hepatocyte endocytic vesicles [J].
Crespo, A ;
Peydró, A ;
Dasí, F ;
Benet, M ;
Calvete, JJ ;
Revert, F ;
Aliño, SF .
GENE THERAPY, 2005, 12 (11) :927-935