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)

Author:

Lee Hong Jun12,Won Jong Ho3,Doo Seung Hwan4,Kim Jung Hoon5,Song Ki Young6,Lee Sun Ju7,Lim Inja8,Chang Kyu-Tae9,Song Yun Seob4,Kim Seung U.12

Affiliation:

1. Medical Research Institute, Chung-Ang University College of Medicine, Seoul, Korea

2. Division of Neurology, Department of Medicine, UBC Hospital, University of British Columbia, Vancouver, Canada

3. ‡Department of Internal Medicine, Soonchunhyang University School of Medicine, Seoul, Korea

4. Department of Urology, Soonchunhyang University School of Medicine, Seoul, Korea

5. Department of Radiology, Soonchunhyang University School of Medicine, Seoul, Korea

6. Avon Old Farms School, Avon, CT, USA

7. Kyunghee University School of Medicine, Seoul, Korea

8. Department of Physiology, Chung-Ang University College of Medicine, Seoul, Korea

9. National Primate Research Center, Korea Research Institute of Bioscience and Biotechnology, Ochang, Korea

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 1: control, group 2: sham operation, group 3: BOO, and group 4: BOO rats receiving SPION-hMSCs). Two weeks after the onset of BOO, 1 × 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-β 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.

Publisher

SAGE Publications

Subject

Transplantation,Cell Biology,Biomedical Engineering

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