RRC ID 117
Author Takeda S, Takahashi M, Mizukami H, Kobayashi E, Takeuchi K, Hakamata Y, Kaneko T, Yamamoto H, Ito C, Ozawa K, Ishibashi K, Matsuzaki T, Takata K, Asano Y, Kusano E.
Title Successful gene transfer using adeno-associated virus vectors into the kidney: comparison among adeno-associated virus serotype 1-5 vectors in vitro and in vivo.
Journal Nephron Exp Nephrol
Abstract BACKGROUND/AIM:Gene transfer into the kidney has great potential as a novel therapeutic approach. However, an efficient method of gene transfer into the kidney has not been established. We explored the transduction efficiency of renal cells in vitro and in vivo using adeno-associated virus (AAV) serotype 1-5 vectors encoding the beta-galactosidase gene.
METHODS:In the in vitro study, rat kidney epithelial cell line NRK52E cells were transfected with AAV serotype derived vectors. In the in vivo study, AAV serotype derived vectors were selectively injected into the kidney using a catheter-based gene delivery system in rats and mice mimicking the clinical procedure. The efficiency of gene expression was histologically evaluated on the basis of the beta-galactosidase expression.
RESULTS:AAV serotype 1, 2, and 5 vectors transduced in rat kidney epithelial cell line NRK52E cells in vitro, whereas AAV serotype 3 or 4 vectors showed no transduction. In addition, the kidney-specific injection of AAV serotype 2 vectors successfully transduced in tubular epithelial cells, but not in glomerular, blood vessel, or interstitial cells in vivo, whereas the rest of the serotypes showed no transduction.
CONCLUSION:Since kidney-specific gene delivery via the renal artery by catheterization is highly feasible in humans, these findings provide useful information for promising strategies in renal gene therapy.
Volume 96(4)
Pages e119-26
Published 2004-1-1
DOI 10.1159/000077378
PII 77378
PMID 15122061
MeSH Animals Catheterization Cell Line Dependovirus / classification Dependovirus / genetics* Genetic Vectors* / administration & dosage Kidney / anatomy & histology Kidney / metabolism* Male Mice Rats Rats, Inbred Lew Transduction, Genetic / methods*
IF 2.238
Times Cited 39
WOS Category UROLOGY & NEPHROLOGY
Resource
Rats