Magnetic resonance imaging of viral particle biodistribution in vivo

被引:43
作者
Raty, J. K.
Liimatainen, T.
Wirth, T.
Airenne, K. J.
Ihalainen, T. O.
Huhtala, T.
Hamerlynck, E.
Vihinen-Ranta, M.
Narvanen, A.
Yla-Herttuala, S.
Hakumaki, J. M.
机构
[1] Univ Kuopio, Dept Biotechnol & Mol Med, FIN-70211 Kuopio, Finland
[2] Ark Therapeut Oy, Kuopio, Finland
[3] AI Virtanen Inst Mol Sci, Dept Biomed NMR, Cellular & Mol Imaging Grp, Kuopio, Finland
[4] Univ Jyvaskyla, Dept Biol & Environm Sci, Jyvaskyla, Finland
[5] Univ Kuopio, Dept Chem, FIN-70211 Kuopio, Finland
[6] Univ Kuopio, Dept Med, SF-70210 Kuopio, Finland
[7] Univ Kuopio, Gene Therapy Unit, SF-70210 Kuopio, Finland
[8] Univ Kuopio, Dept Clin Radiol, SF-70210 Kuopio, Finland
关键词
baculovirus; MRI; avidin; biodistribution; imaging;
D O I
10.1038/sj.gt.3302828
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 describe here a technique for the visualization of viral vector delivery by magnetic resonance imaging (MRI) in vivo. By conjugating avidin-coated baculoviral vectors (Baavi) with biotinylated ultra-small superparamagnetic iron oxide particles (USPIO), we are able to produce vector-related MRI contrast in the choroid plexus cells of rat brain in vivo over a period of 14 days. Ten microlitres of 2.5 x 10(10) PFU/ml nuclear-targeted LacZ-encoding Baavi with bUSPIO coating was injected into rat brain ventricles and visualized by MRI at 4.7 T. As baculoviruses exhibit restricted cell-type specificity in the rat brain, altered MRI contrast was detected in the choroid plexus of the injected ventricles. No specific signal loss was detected when wild-type baculoviruses or intact biotinylated USPIO particles were injected into the lateral ventricles. Cryosectioned brains were stained for nuclear-targeted beta-galactosidase gene expression, which was found to colocalize with MRI contrast. This study provides the first proof of principle for robust and non-invasive viral vector MRI by using avidin-displaying viruses in vivo. Considering the widespread use of MRI in current medical imaging, the approach is likely to provide numerous future applications in imaging of therapeutic gene transfer.
引用
收藏
页码:1440 / 1446
页数:7
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