Injection of Dental Pulp Stem Cells Promotes Healing of Damaged Bladder Tissue in a Rat Model of Chemically Induced Cystitis

Dental pulp stem cells (DPSCs) are reported as sources of mesenchymal stem cells (MSCs). MSCs are used as cell therapy options for various diseases. The present study examined the healing effects of DPSC injection on damaged bladder tissue in a chemically induced cystitis rat model. Cystitis was ind...

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Main Authors: Yujiro Hirose, Tokunori Yamamoto, Misako Nakashima, Yasuhito Funahashi, Yoshihisa Matsukawa, Masaya Yamaguchi, Shigetada Kawabata, Momokazu Gotoh
Format: Article
Language:English
Published: SAGE Publishing 2016-03-01
Series:Cell Transplantation
Online Access:https://doi.org/10.3727/096368915X689523
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spelling doaj-64f962452a9a49f6b4fe1c0e4f9739ed2020-11-25T03:15:10ZengSAGE PublishingCell Transplantation0963-68971555-38922016-03-012510.3727/096368915X689523Injection of Dental Pulp Stem Cells Promotes Healing of Damaged Bladder Tissue in a Rat Model of Chemically Induced CystitisYujiro Hirose0Tokunori Yamamoto1Misako Nakashima2Yasuhito Funahashi3Yoshihisa Matsukawa4Masaya Yamaguchi5Shigetada Kawabata6Momokazu Gotoh7Department of Oral and Molecular Microbiology, Osaka University Graduate School of Dentistry, Suita, JapanDepartment of Urology, Nagoya University Graduate School of Medicine, Nagoya, JapanDepartment of Dental Regenerative Medicine, Center of Advanced Medicine for Dental and Oral Diseases, National Center for Geriatrics and Gerontology, Obu, JapanDepartment of Urology, Nagoya University Graduate School of Medicine, Nagoya, JapanDepartment of Urology, Nagoya University Graduate School of Medicine, Nagoya, JapanDepartment of Oral and Molecular Microbiology, Osaka University Graduate School of Dentistry, Suita, JapanDepartment of Oral and Molecular Microbiology, Osaka University Graduate School of Dentistry, Suita, JapanDepartment of Urology, Nagoya University Graduate School of Medicine, Nagoya, JapanDental pulp stem cells (DPSCs) are reported as sources of mesenchymal stem cells (MSCs). MSCs are used as cell therapy options for various diseases. The present study examined the healing effects of DPSC injection on damaged bladder tissue in a chemically induced cystitis rat model. Cystitis was induced by hydrochloride injection into the bladder of female F344/NSlc rats. On the following day, DPSCs suspended in phosphate-buffered saline (PBS) were injected into the bladder and maintained for 1 h (DPSC injection group), while PBS alone was injected as the standard for comparison (PBS injection group). After 2 days following injection, considerable submucosal edema, vascular structure destruction, hemorrhage, and inflammatory cell invasion were observed both in the DPSC and PBS injection groups, with no difference in their degree of submucosal edema and hemorrhage. Six days after injection, vascular structure regeneration was observed in both groups; however, unlike the DPSC injection group, the PBS injection group showed traces of submucosal edema and hemorrhage. These results correlated with tissue concentrations of myeloperoxidase (MPO) and the inflammatory cytokines IL-1β, IL-6, and TNF-α. Furthermore, the intercontraction interval was prolonged, and the frequency of nociceptive behaviors was reduced in the DPSC injection group compared with the PBS injection group. DPSCs were found on the bladder epithelium until day 3 after injection. In the DPSC-conditioned media (CM), the trophic factors FGF-2, VEGF, and the C-C and C-X-C families of chemokines were detected. The results of DPSC injection into the cystitis rat model suggested that the injected cells promote the healing of the damaged bladder tissue by exerting various trophic effects while localizing on the bladder epithelium and that MSC injection is a potential novel therapy for interstitial cystitis/painful bladder syndrome.https://doi.org/10.3727/096368915X689523
collection DOAJ
language English
format Article
sources DOAJ
author Yujiro Hirose
Tokunori Yamamoto
Misako Nakashima
Yasuhito Funahashi
Yoshihisa Matsukawa
Masaya Yamaguchi
Shigetada Kawabata
Momokazu Gotoh
spellingShingle Yujiro Hirose
Tokunori Yamamoto
Misako Nakashima
Yasuhito Funahashi
Yoshihisa Matsukawa
Masaya Yamaguchi
Shigetada Kawabata
Momokazu Gotoh
Injection of Dental Pulp Stem Cells Promotes Healing of Damaged Bladder Tissue in a Rat Model of Chemically Induced Cystitis
Cell Transplantation
author_facet Yujiro Hirose
Tokunori Yamamoto
Misako Nakashima
Yasuhito Funahashi
Yoshihisa Matsukawa
Masaya Yamaguchi
Shigetada Kawabata
Momokazu Gotoh
author_sort Yujiro Hirose
title Injection of Dental Pulp Stem Cells Promotes Healing of Damaged Bladder Tissue in a Rat Model of Chemically Induced Cystitis
title_short Injection of Dental Pulp Stem Cells Promotes Healing of Damaged Bladder Tissue in a Rat Model of Chemically Induced Cystitis
title_full Injection of Dental Pulp Stem Cells Promotes Healing of Damaged Bladder Tissue in a Rat Model of Chemically Induced Cystitis
title_fullStr Injection of Dental Pulp Stem Cells Promotes Healing of Damaged Bladder Tissue in a Rat Model of Chemically Induced Cystitis
title_full_unstemmed Injection of Dental Pulp Stem Cells Promotes Healing of Damaged Bladder Tissue in a Rat Model of Chemically Induced Cystitis
title_sort injection of dental pulp stem cells promotes healing of damaged bladder tissue in a rat model of chemically induced cystitis
publisher SAGE Publishing
series Cell Transplantation
issn 0963-6897
1555-3892
publishDate 2016-03-01
description Dental pulp stem cells (DPSCs) are reported as sources of mesenchymal stem cells (MSCs). MSCs are used as cell therapy options for various diseases. The present study examined the healing effects of DPSC injection on damaged bladder tissue in a chemically induced cystitis rat model. Cystitis was induced by hydrochloride injection into the bladder of female F344/NSlc rats. On the following day, DPSCs suspended in phosphate-buffered saline (PBS) were injected into the bladder and maintained for 1 h (DPSC injection group), while PBS alone was injected as the standard for comparison (PBS injection group). After 2 days following injection, considerable submucosal edema, vascular structure destruction, hemorrhage, and inflammatory cell invasion were observed both in the DPSC and PBS injection groups, with no difference in their degree of submucosal edema and hemorrhage. Six days after injection, vascular structure regeneration was observed in both groups; however, unlike the DPSC injection group, the PBS injection group showed traces of submucosal edema and hemorrhage. These results correlated with tissue concentrations of myeloperoxidase (MPO) and the inflammatory cytokines IL-1β, IL-6, and TNF-α. Furthermore, the intercontraction interval was prolonged, and the frequency of nociceptive behaviors was reduced in the DPSC injection group compared with the PBS injection group. DPSCs were found on the bladder epithelium until day 3 after injection. In the DPSC-conditioned media (CM), the trophic factors FGF-2, VEGF, and the C-C and C-X-C families of chemokines were detected. The results of DPSC injection into the cystitis rat model suggested that the injected cells promote the healing of the damaged bladder tissue by exerting various trophic effects while localizing on the bladder epithelium and that MSC injection is a potential novel therapy for interstitial cystitis/painful bladder syndrome.
url https://doi.org/10.3727/096368915X689523
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