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Gene delivery into rat glomerulus using a mesangial cell vector

Authors
Kim, H.J.Kim, S.I.Yun, I.J.Kwak, J.H.Yu, S.H.
Issue Date
Dec-2000
Publisher
SPRINGER-VERLAG SINGAPORE PTE LTD
Keywords
beta-galactosidase; ex vivo gene transfer; mesangial cell vector; retrovirus; specific targeting to glomeruli
Citation
MOLECULES AND CELLS, v.10, no.6, pp 662 - 668
Pages
7
Journal Title
MOLECULES AND CELLS
Volume
10
Number
6
Start Page
662
End Page
668
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/47340
DOI
10.1007/s100590000027
ISSN
1016-8478
0219-1032
Abstract
To develop an effective protocol of gene transfer into glomeruli, an ex vivo gene delivery system using rat mesangial cells (RMC) as a vector was examined. RMC genetically engineered with a retrovirus harboring the Escherichia coli beta -galactosidase gene was used to estimate the efficacy of gene delivery and the location of the cells within the kidney. The RMC expressing beta -galactosidase, RMCLZ1, was cultured in vitro and the cells were injected into the left kidney through the renal artery of a normal Sprague Dawley rat. At least 1 x 10(6) RMCLZ1 was required for effective gene delivery into glomeruli. One hour and 1, 4, and 14 d after injection, glomeruli were isolated from the left kidneys injected with the cells and the expression of beta -galactosidase in each glomeruli was evaluated. One hour and 1 d after injection, more than 90 and 80%, respectively, of glomeruli from the left kidney showed strong beta -galactosidase activity, white no activity of beta -galactosidase was found in the glomeruti from the right kidneys. The number of glomeruli stained by X-gat and the intensity decreased with time. Fourteen days after injection, about 35% of the glomeruli retained the RMCLZ1. X-gal and periodic acid-Schiff staining of frozen sections obtained 14 d after injection allowed the estimation of the site where the mesangial cells injected were located. The mesangial cells were found mainly in two different locations, the glomerular capillary and the mesangium. The majority (about 90%) of the mesangial cells were located in the glomerular capillary and about 9% of the cells were in the mesangial area. Occasionally, the positive staining was found in proximal tubules and the interlobular artery. Although additional methods are required for the site-specific targeting of the mesangial area, the ex vivo gene transfer to glomeruli is feasible and may be a useful tool for future investigations in the pathological mechanisms of glomerular injury.
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