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Inhibition of Collagen Deposit in Obstructed Rat Bladder Outlet by Transplantation of Superparamagnetic Iron Oxide-Labeled Human Mesenchymal Stem Cells as Monitored by Molecular Magnetic Resonance Imaging (MRI)

Authors
Lee, Hong JunWon, Jong HoDoo, Seung HwanKim, Jung HoonSong, Ki YoungLee, Sun JuLim, InjaChang, Kyu-TaeSong, Yun SeobKim, Seung U.
Issue Date
2012
Publisher
Cognizant Communication Corp.
Keywords
Bladder outlet obstruction; Human mesenchymal stem cells (MSCs); Collagen; Transforming growth factor-beta (TGF-beta); Superparamagnetic iron oxide nanoparticle (SPION); Magnetic resonance imaging (MRI); Cell transplantation
Citation
Cell Transplantation, v.21, no.5, pp 959 - 970
Pages
12
Journal Title
Cell Transplantation
Volume
21
Number
5
Start Page
959
End Page
970
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/15981
DOI
10.3727/096368911X627516
ISSN
0963-6897
1555-3892
Abstract
Bladder outlet obstruction (BOO) caused by collagen deposit is one of the most common problems in elderly males. The present study is to investigate if human mesenchymal stem cells (MSCs) are capable of inhibiting collagen deposition and improve cystometric parameters in bladder outlet obstruction in rats. Human MSCs were labeled with nanoparticles containing superparamagnetic iron oxide (SPION), and transplanted in rat BOO lesion site. Forty 6-week-old female Sprague-Dawley rats were divided into four groups (group I: control, group 2: sham operation, group 3: BOO, and group 4: BOO rats receiving SPION-hMSCs). Two weeks after the onset of BOO, 1 x 106 SPION-hMSCs were injected into the bladder wall. Serial T2-weighted MR images were taken immediately after transplantation of SPION-labeled human MSCs and at 4 weeks posttransplantation. T2-weighted MR images showed a clear hypointense signal induced by the SPION-labeled MSCs. While the expression of collagen and TGF-beta protein increased after BOO, the expression of both returned to the original levels after MSC transplantation. Expression of HGF and c-met protein also increased in the group with MSC transplantation. Maximal voiding pressure and residual urine volume increased after BOO but they recovered after MSC transplantation. Human MSCs transplanted in rat BOO models inhibited the bladder fibrosis and mediated recovery of bladder dysfunction. Transplantation of MSC-based cell therapy could be a novel therapeutic strategy against bladder fibrosis in patients with bladder outlet obstruction.
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