Recombinant adeno-associated virus vectors efficiently transduce foreign gene into bovine aortic endothelial cells: Comparison with adenovirus vectors

Citation
S. Teramoto et al., Recombinant adeno-associated virus vectors efficiently transduce foreign gene into bovine aortic endothelial cells: Comparison with adenovirus vectors, JPN J PHARM, 84(2), 2000, pp. 206-212
Citations number
33
Categorie Soggetti
Pharmacology & Toxicology
Journal title
JAPANESE JOURNAL OF PHARMACOLOGY
ISSN journal
00215198 → ACNP
Volume
84
Issue
2
Year of publication
2000
Pages
206 - 212
Database
ISI
SICI code
0021-5198(200010)84:2<206:RAVVET>2.0.ZU;2-J
Abstract
Because the features and kinetics of adeno-associated virus (AAV)-mediated gene transfer to endothelial cells (EC) are yet to be ultimately determined , we tested variables pertinent to the efficiency of AAV-mediated gene tran sfer to bovine aortic endothelial cells (BAEC). The variables with AAV vect ors were compared with the better characterized adenovirus (Ad) vectors. Th ere is a dose-response relationship between multiplicity of infection (moi) of AAV or Ad vectors and transduction efficiency in BAEC. The higher moi o f AAV vectors achieved more than 80% of transduction efficiency in cultured BAEC. AAV and Ad vectors showed an incubation-time-dependent increase in t ransduction efficiency of LacZ gene to the BAEC up to 12 h of vector exposu re. Although the similar kinetics of transduction efficiency of LacZ gene t o BAEC was found in both vectors, the duration of gene expression was longe r in AAV vector than that in Ad vectors in vitro. These results indicate th at AAV-vector is efficient for gene transfer to EC, and higher moi of vecto rs or a longer period exposure of vectors to EC can facilitate efficient tr ansduction of a foreign gene into cultured EC. For the duration of gene exp ression, the AAV vectors may be better than Ad vectors.