DNA/dendrimer complexes mediate gene transfer into murine cardiac transplants ex vivo

被引:35
作者
Wang, YO
Boros, P
Liu, JH
Qin, LH
Bai, YL
Bielinska, AU
Kukowska-Latallo, JF
Baker, JR
Bromberg, JS
机构
[1] CUNY Mt Sinai Sch Med, Inst Gene Therapy & Mol Med, New York, NY 10029 USA
[2] CUNY Mt Sinai Sch Med, Recanati Miller Transplantat Inst, New York, NY 10029 USA
[3] Univ Michigan, Ctr Biol Nanotechnol, Ann Arbor, MI 48105 USA
关键词
gene transfer; dendrimer; plasmid DNA; transplantation;
D O I
10.1006/mthe.2000.0201
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
Starburst polyamidoamine dendrimers are synthetic polymers with unique structural and physical characteristics suitable for DNA gene transfer. Our previous studies demonstrated that Starburst dendrimers augment plasmid-mediated gene transfer efficiency in a nonvascularized, cardiac transplantation model. In this study, the fifth generation of ethylenediamine core dendrimer was investigated for its ability to enhance gene transfer and expression in a clinically relevant murine vascularized heart transplantation model. The plasmid pMP6A-beta -gal, encoding beta -galactosidase (beta -cal), was incubated with dendrimers to form complexes. The complexes were perfused via the coronary arteries during donor graft harvesting, and reporter gene expression was determined by quantitative evaluation of X-Gal staining. The grafts infused with pMP6A-beta -gal/dendrimer complexes showed beta -Gal expression in myocytes from 7 to 14 days. A number of variables for transfer of the DNA/dendrimer complexes were tested, including DNA:dendrimer charge ratios, concentrations of DNA and dendrimer, preservation solutions, ischemic time, and enhancement of vascular permeability by serotonin, papaverine, and VEGF administration. The results showed that DNA/dendrimer complexes containing 20 mug of DNA and 260 mug of dendrimer (1:20 charge ratio) in a total volume of 200 mul resulted in highest gene expression in the grafts. The results also showed that prolonged incubation (cold ischemic time) to 2 h and pretreatment with serotonin further enhanced gene expression.
引用
收藏
页码:602 / 608
页数:7
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