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Recombinant insulin-like growth factor-1 activates satellite cells in the mouse urethral rhabdosphincter

BACKGROUND: The goal of this study is to demonstrate the efficacy of a new method for the treatment of urinary incontinence by stimulation of urethral rhabdosphincter satellite cells. We show that satellite cells do exist in the sphincter muscle of retired male mice breeders by staining for c-Met, a...

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Autores principales: Wei, Wenjie, Howard, Pamela S, Macarak, Edward J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3907012/
https://www.ncbi.nlm.nih.gov/pubmed/24279352
http://dx.doi.org/10.1186/1471-2490-13-62
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author Wei, Wenjie
Howard, Pamela S
Macarak, Edward J
author_facet Wei, Wenjie
Howard, Pamela S
Macarak, Edward J
author_sort Wei, Wenjie
collection PubMed
description BACKGROUND: The goal of this study is to demonstrate the efficacy of a new method for the treatment of urinary incontinence by stimulation of urethral rhabdosphincter satellite cells. We show that satellite cells do exist in the sphincter muscle of retired male mice breeders by staining for c-Met, a satellite cell specific protein. Once activated by recombinant mouse Insulin-like Growth Factor-1(rIgf-1), the satellite cells develop into muscle cells within the rhabdosphincter thereby potentially strengthening it. METHODS: 20 μl (1 μg/μl) of rIgf-1 was surgically injected directly into the urethral wall of retired male mouse breeders. Mice injected with phosphate buffered saline (PBS) were used as controls. 4 weeks later, urethras were harvested and serially-sectioned through the sphincter for routine hematoxylin-eosin staining as well as immunohistochemical staining with satellite cell specific anti-c-Met antibody and proliferation specific anti-Ki-67 antibody. RESULTS: Anti-c-Met antibody positive cells (c-Met(+)) were identified in the rhabdosphincter. c-Met(+) cells increased by 161.8% relative to controls four weeks after rIGF-1 injection. Anti- Ki-67 antibody positive cells were identified and characterized as cells with centrally located nuclei in striated muscle bundles of rIGF-1 treated animals. CONCLUSIONS: Satellite cells in the mouse rhabdosphincter can be activated by rIGF-1 treatment, which subsequently are incorporated into existing skeletal muscle bundles. Using this approach, the rhabdosphincter can be induced to regenerate and potentially strengthen via satellite cell activation and likely improve urinary continence.
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spelling pubmed-39070122014-01-31 Recombinant insulin-like growth factor-1 activates satellite cells in the mouse urethral rhabdosphincter Wei, Wenjie Howard, Pamela S Macarak, Edward J BMC Urol Research Article BACKGROUND: The goal of this study is to demonstrate the efficacy of a new method for the treatment of urinary incontinence by stimulation of urethral rhabdosphincter satellite cells. We show that satellite cells do exist in the sphincter muscle of retired male mice breeders by staining for c-Met, a satellite cell specific protein. Once activated by recombinant mouse Insulin-like Growth Factor-1(rIgf-1), the satellite cells develop into muscle cells within the rhabdosphincter thereby potentially strengthening it. METHODS: 20 μl (1 μg/μl) of rIgf-1 was surgically injected directly into the urethral wall of retired male mouse breeders. Mice injected with phosphate buffered saline (PBS) were used as controls. 4 weeks later, urethras were harvested and serially-sectioned through the sphincter for routine hematoxylin-eosin staining as well as immunohistochemical staining with satellite cell specific anti-c-Met antibody and proliferation specific anti-Ki-67 antibody. RESULTS: Anti-c-Met antibody positive cells (c-Met(+)) were identified in the rhabdosphincter. c-Met(+) cells increased by 161.8% relative to controls four weeks after rIGF-1 injection. Anti- Ki-67 antibody positive cells were identified and characterized as cells with centrally located nuclei in striated muscle bundles of rIGF-1 treated animals. CONCLUSIONS: Satellite cells in the mouse rhabdosphincter can be activated by rIGF-1 treatment, which subsequently are incorporated into existing skeletal muscle bundles. Using this approach, the rhabdosphincter can be induced to regenerate and potentially strengthen via satellite cell activation and likely improve urinary continence. BioMed Central 2013-11-26 /pmc/articles/PMC3907012/ /pubmed/24279352 http://dx.doi.org/10.1186/1471-2490-13-62 Text en Copyright © 2013 Wei et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Wei, Wenjie
Howard, Pamela S
Macarak, Edward J
Recombinant insulin-like growth factor-1 activates satellite cells in the mouse urethral rhabdosphincter
title Recombinant insulin-like growth factor-1 activates satellite cells in the mouse urethral rhabdosphincter
title_full Recombinant insulin-like growth factor-1 activates satellite cells in the mouse urethral rhabdosphincter
title_fullStr Recombinant insulin-like growth factor-1 activates satellite cells in the mouse urethral rhabdosphincter
title_full_unstemmed Recombinant insulin-like growth factor-1 activates satellite cells in the mouse urethral rhabdosphincter
title_short Recombinant insulin-like growth factor-1 activates satellite cells in the mouse urethral rhabdosphincter
title_sort recombinant insulin-like growth factor-1 activates satellite cells in the mouse urethral rhabdosphincter
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3907012/
https://www.ncbi.nlm.nih.gov/pubmed/24279352
http://dx.doi.org/10.1186/1471-2490-13-62
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