Using magnetic forces to enhance non-viral gene transfer to airway epithelium in vivo

被引:67
作者
Xenariou, S.
Griesenbach, U.
Ferrari, S.
Dean, P.
Scheule, R. K.
Cheng, S. H.
Geddes, D. M.
Plank, C.
Alton, E. W. F. W.
机构
[1] Univ London Imperial Coll Sci & Technol, Natl Heart & Lung Inst, Dept Gene Therapy, Fac Med, London SW3 6LR, England
[2] Genzyme Corp, Framingham, MA 01701 USA
[3] Tech Univ Munich, Inst Expt Oncol, D-8000 Munich, Germany
关键词
magnetofection; physical methods; non-viral vectors; airway epithelium; cystic fibrosis;
D O I
10.1038/sj.gt.3302803
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
We have assessed whether magnetic forces (magnetofection) can enhance non-viral gene transfer to the airways. TransMAG(PEI), a superparamagnetic particle was coupled to Lipofectamine 2000 or cationic lipid 67 (GL67)/plasmid DNA (pDNA) liposome complexes. In vitro transfection with these formulations resulted in approximately 300- and 30-fold increase in reporter gene expression, respectively, after exposure to a magnetic field, but only at suboptimal pDNA concentrations. Because GL67 has been formulated for in vivo use, we next assessed TransMAG(PEI) in the murine nasal epithelium in vivo, and compared this to naked pDNA. At the concentrations required for in vivo experiments, precipitation of magnetic complexes was seen. After extensive optimization, addition of non-precipitated magnetic particles resulted in approximately seven- and 90-fold decrease in gene expression for naked pDNA and GL67/pDNA liposome complexes, respectively, compared to non-magnetic particles. Thus, whereas exposure to a magnetic field improved in vitro transfection efficiency, translation to the in vivo setting remains difficult.
引用
收藏
页码:1545 / 1552
页数:8
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