Improvement in Spinal Cord Injury-Induced Bladder Fibrosis Using Mesenchymal Stem Cell Transplantation into the Bladder Wall

Author:

Lee Hong Jun1,An Jin1,Doo Seung Whan2,Kim Jae Heon2,Choi Sung Sik1,Lee Sang-Rae3,Park Seung Won4,Song Yun Seob2,Kim Seung U.15

Affiliation:

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

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

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

4. Department of Neurosurgery, Chung-Ang University College of Medicine, Seoul, Korea

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

Abstract

Experiments on spinal cord injury (SCI) have largely focused on the transplantation of stem cells into injured spinal cords for motor recovery while neglecting to investigate bladder dysfunction. The present study was performed to investigate the effect of B10 human mesenchymal stem cells (hMSCs) directly transplanted into the bladder wall of SCI rats and to determine whether they are capable of inhibiting collagen deposition and improving cystometric parameters in SCI rats. Forty 6-week-old female Sprague–Dawley rats were divided into four groups (group 1: control, group 2: sham operated, group 3: SCI, group 4: SCI rats that received B10 cells). B10 cells were labeled with fluorescent magnetic nanoparticles (MNPs). Four weeks after the onset of SCI, MNP-labeled B10 cells were injected to the bladder wall. Serial magnetic resonance (MR) images were taken immediately after MNP-B10 injection and at 4 weeks posttransplantation. Voiding function was assessed at 4 weeks posttransplantation, and the bladder was harvested. Improvements in bladder fibrosis and bladder function were monitored by molecular MR imaging. Transplantation of B10 cells into the SCI rats markedly reduced their weights and collagen deposition. MR images showed a clear hypointense signal induced by the MNP-labeled B10 cells at 4 weeks posttransplantation. Transplanted B10 cells were found to differentiate into smooth muscle cells. The intercontraction interval decreased, and the maximal voiding pressure increased after SCI but recovered after B10 cell transplantation. Survival of B10 cells was found at 4 weeks posttransplantation using anti-human mitochondria antibody staining and MR imaging. The transplanted B10 cells inhibited bladder fibrosis and ameliorated bladder dysfunction in the rat SCI model. MSC-based cell transplantation may be a novel therapeutic strategy for bladder dysfunction in patients with SCI.

Publisher

SAGE Publications

Subject

Transplantation,Cell Biology,Biomedical Engineering

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