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The effect of a cyclic uniaxial strain on urinary bladder cells
PURPOSE: Pre-conditioning of a cell seeded construct may improve the functional outcome of a tissue engineered construct for augmentation cystoplasty. The precise effects of mechanical stimulation on urinary bladder cells in vitro are not clear. In this study we investigate the effect of a cyclic un...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613063/ https://www.ncbi.nlm.nih.gov/pubmed/28229212 http://dx.doi.org/10.1007/s00345-017-2013-9 |
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author | Tiemessen, Dorien de Jonge, Paul Daamen, Willeke Feitz, Wout Geutjes, Paul Oosterwijk, Egbert |
author_facet | Tiemessen, Dorien de Jonge, Paul Daamen, Willeke Feitz, Wout Geutjes, Paul Oosterwijk, Egbert |
author_sort | Tiemessen, Dorien |
collection | PubMed |
description | PURPOSE: Pre-conditioning of a cell seeded construct may improve the functional outcome of a tissue engineered construct for augmentation cystoplasty. The precise effects of mechanical stimulation on urinary bladder cells in vitro are not clear. In this study we investigate the effect of a cyclic uniaxial strain culture on urinary bladder cells which were seeded on a type I collagen scaffold. METHODS: Isolated porcine smooth muscle cells or urothelial cells were seeded on a type I collagen scaffolds and cultured under static and dynamic conditions. A uniform cyclic uniaxial strain was applied to the seeded scaffold using a Bose Electroforce Bio-Dynamic bioreactor. Cell proliferation rate and phenotype were investigated, including SEM analysis, RT-PCR and immunohistochemistry for α-Smooth muscle actin, calponin-1, desmin and RCK103 expression to determine the effects of mechanical stimulation on both cell types. RESULTS: Dynamic stimulation of smooth muscle cell seeded constructs resulted in cell alignment and enhanced proliferation rate. Additionally, expression of α-Smooth muscle actin and calponin-1 was increased suggesting differentiation of smooth muscle cells to a more mature phenotype. CONCLUSIONS: Mechanical stimuli did not enhance the proliferation and differentiation of urothelial cells. Mechanical stimulation, i.e., preconditioning may improve the functional in vivo outcome of smooth muscle cell seeded constructs for flexible organs such as the bladder. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00345-017-2013-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5613063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-56130632017-10-10 The effect of a cyclic uniaxial strain on urinary bladder cells Tiemessen, Dorien de Jonge, Paul Daamen, Willeke Feitz, Wout Geutjes, Paul Oosterwijk, Egbert World J Urol Original Article PURPOSE: Pre-conditioning of a cell seeded construct may improve the functional outcome of a tissue engineered construct for augmentation cystoplasty. The precise effects of mechanical stimulation on urinary bladder cells in vitro are not clear. In this study we investigate the effect of a cyclic uniaxial strain culture on urinary bladder cells which were seeded on a type I collagen scaffold. METHODS: Isolated porcine smooth muscle cells or urothelial cells were seeded on a type I collagen scaffolds and cultured under static and dynamic conditions. A uniform cyclic uniaxial strain was applied to the seeded scaffold using a Bose Electroforce Bio-Dynamic bioreactor. Cell proliferation rate and phenotype were investigated, including SEM analysis, RT-PCR and immunohistochemistry for α-Smooth muscle actin, calponin-1, desmin and RCK103 expression to determine the effects of mechanical stimulation on both cell types. RESULTS: Dynamic stimulation of smooth muscle cell seeded constructs resulted in cell alignment and enhanced proliferation rate. Additionally, expression of α-Smooth muscle actin and calponin-1 was increased suggesting differentiation of smooth muscle cells to a more mature phenotype. CONCLUSIONS: Mechanical stimuli did not enhance the proliferation and differentiation of urothelial cells. Mechanical stimulation, i.e., preconditioning may improve the functional in vivo outcome of smooth muscle cell seeded constructs for flexible organs such as the bladder. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00345-017-2013-9) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-02-23 2017 /pmc/articles/PMC5613063/ /pubmed/28229212 http://dx.doi.org/10.1007/s00345-017-2013-9 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Tiemessen, Dorien de Jonge, Paul Daamen, Willeke Feitz, Wout Geutjes, Paul Oosterwijk, Egbert The effect of a cyclic uniaxial strain on urinary bladder cells |
title | The effect of a cyclic uniaxial strain on urinary bladder cells |
title_full | The effect of a cyclic uniaxial strain on urinary bladder cells |
title_fullStr | The effect of a cyclic uniaxial strain on urinary bladder cells |
title_full_unstemmed | The effect of a cyclic uniaxial strain on urinary bladder cells |
title_short | The effect of a cyclic uniaxial strain on urinary bladder cells |
title_sort | effect of a cyclic uniaxial strain on urinary bladder cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613063/ https://www.ncbi.nlm.nih.gov/pubmed/28229212 http://dx.doi.org/10.1007/s00345-017-2013-9 |
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