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Human amniotic fluid stem cells can alleviate detrusor dysfunction caused by bladder outlet obstruction in rats

The present study examined whether bladder detrusor dysfunction due to partial bladder outlet obstruction (pBOO) could be improved after the treatment of human amniotic fluid stem cells (hAFSCs). 72 female rats were grouped into sham operation, pBOO, and pBOO with hAFSCs treatment (pBOO + hAFSCs) fo...

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Autores principales: Liang, Ching-Chung, Huang, Wen-Chu, Shaw, Steven W., Huang, Yung-Hsin, Lee, Tsong-Hai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9035144/
https://www.ncbi.nlm.nih.gov/pubmed/35461349
http://dx.doi.org/10.1038/s41598-022-10640-y
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author Liang, Ching-Chung
Huang, Wen-Chu
Shaw, Steven W.
Huang, Yung-Hsin
Lee, Tsong-Hai
author_facet Liang, Ching-Chung
Huang, Wen-Chu
Shaw, Steven W.
Huang, Yung-Hsin
Lee, Tsong-Hai
author_sort Liang, Ching-Chung
collection PubMed
description The present study examined whether bladder detrusor dysfunction due to partial bladder outlet obstruction (pBOO) could be improved after the treatment of human amniotic fluid stem cells (hAFSCs). 72 female rats were grouped into sham operation, pBOO, and pBOO with hAFSCs treatment (pBOO + hAFSCs) for in vitro and in vivo studies. Bladder weight, bladder wall thickness, the ratio of collagen to smooth muscle and the levels of positive CD11b/c and HIS48 cells was significantly increased after pBOO but improved after hAFSCs treatment. Cystometries showed impaired bladder function after pBOO. Protein and mRNA levels of hypoxia inducible factor-1α, CCL2, interleukin-1β, transforming growth factor-β1 (TGF-β1), connective tissue growth factor (CTGF), α-smooth muscle actin, collagen I and collagen III were increased at 2 and/or 6 weeks, but proteins and mRNA expressions of protein gene product 9.5 were decreased at 2 and 6 weeks after pBOO. These abnormalities were improved after hAFSCs treatment. The expressions of TGF-β1 and CTGF in cultured detrusor cells of pBOO rats were increased but were improved after hAFSCs treatment. The present results showed hAFSCs treatment could improve bladder detrusor dysfunction in pBOO rats, which may be related to the reduction of inflammatory and pro-fibrotic markers in detrusor muscle cells.
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spelling pubmed-90351442022-04-27 Human amniotic fluid stem cells can alleviate detrusor dysfunction caused by bladder outlet obstruction in rats Liang, Ching-Chung Huang, Wen-Chu Shaw, Steven W. Huang, Yung-Hsin Lee, Tsong-Hai Sci Rep Article The present study examined whether bladder detrusor dysfunction due to partial bladder outlet obstruction (pBOO) could be improved after the treatment of human amniotic fluid stem cells (hAFSCs). 72 female rats were grouped into sham operation, pBOO, and pBOO with hAFSCs treatment (pBOO + hAFSCs) for in vitro and in vivo studies. Bladder weight, bladder wall thickness, the ratio of collagen to smooth muscle and the levels of positive CD11b/c and HIS48 cells was significantly increased after pBOO but improved after hAFSCs treatment. Cystometries showed impaired bladder function after pBOO. Protein and mRNA levels of hypoxia inducible factor-1α, CCL2, interleukin-1β, transforming growth factor-β1 (TGF-β1), connective tissue growth factor (CTGF), α-smooth muscle actin, collagen I and collagen III were increased at 2 and/or 6 weeks, but proteins and mRNA expressions of protein gene product 9.5 were decreased at 2 and 6 weeks after pBOO. These abnormalities were improved after hAFSCs treatment. The expressions of TGF-β1 and CTGF in cultured detrusor cells of pBOO rats were increased but were improved after hAFSCs treatment. The present results showed hAFSCs treatment could improve bladder detrusor dysfunction in pBOO rats, which may be related to the reduction of inflammatory and pro-fibrotic markers in detrusor muscle cells. Nature Publishing Group UK 2022-04-23 /pmc/articles/PMC9035144/ /pubmed/35461349 http://dx.doi.org/10.1038/s41598-022-10640-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Liang, Ching-Chung
Huang, Wen-Chu
Shaw, Steven W.
Huang, Yung-Hsin
Lee, Tsong-Hai
Human amniotic fluid stem cells can alleviate detrusor dysfunction caused by bladder outlet obstruction in rats
title Human amniotic fluid stem cells can alleviate detrusor dysfunction caused by bladder outlet obstruction in rats
title_full Human amniotic fluid stem cells can alleviate detrusor dysfunction caused by bladder outlet obstruction in rats
title_fullStr Human amniotic fluid stem cells can alleviate detrusor dysfunction caused by bladder outlet obstruction in rats
title_full_unstemmed Human amniotic fluid stem cells can alleviate detrusor dysfunction caused by bladder outlet obstruction in rats
title_short Human amniotic fluid stem cells can alleviate detrusor dysfunction caused by bladder outlet obstruction in rats
title_sort human amniotic fluid stem cells can alleviate detrusor dysfunction caused by bladder outlet obstruction in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9035144/
https://www.ncbi.nlm.nih.gov/pubmed/35461349
http://dx.doi.org/10.1038/s41598-022-10640-y
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