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Acquired contractile ability in human endometrial stromal cells by passive loading of cyclic tensile stretch

The uterus plays an important and unique role during pregnancy and is a dynamic organ subjected to mechanical stimuli. It has been reported that infertility occurs when the peristalsis is prevented, although its mechanisms remain unknown. In this study, we found that mechanical strain mimicking the...

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Autores principales: Kim, Jeonghyun, Ushida, Takashi, Montagne, Kevin, Hirota, Yasushi, Yoshino, Osamu, Hiraoka, Takehiro, Osuga, Yutaka, Furuakwa, Katsuko S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7265371/
https://www.ncbi.nlm.nih.gov/pubmed/32488068
http://dx.doi.org/10.1038/s41598-020-65884-3
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author Kim, Jeonghyun
Ushida, Takashi
Montagne, Kevin
Hirota, Yasushi
Yoshino, Osamu
Hiraoka, Takehiro
Osuga, Yutaka
Furuakwa, Katsuko S.
author_facet Kim, Jeonghyun
Ushida, Takashi
Montagne, Kevin
Hirota, Yasushi
Yoshino, Osamu
Hiraoka, Takehiro
Osuga, Yutaka
Furuakwa, Katsuko S.
author_sort Kim, Jeonghyun
collection PubMed
description The uterus plays an important and unique role during pregnancy and is a dynamic organ subjected to mechanical stimuli. It has been reported that infertility occurs when the peristalsis is prevented, although its mechanisms remain unknown. In this study, we found that mechanical strain mimicking the peristaltic motion of the uterine smooth muscle layer enabled the endometrial stromal cells to acquire contractility. In order to mimic the peristalsis induced by uterine smooth muscle cells, cyclic tensile stretch was applied to human endometrial stromal cells. The results showed that the strained cells exerted greater contractility in three-dimensional collagen gels in the presence of oxytocin, due to up-regulated alpha-smooth muscle actin expression via the cAMP signaling pathway. These in vitro findings underscore the plasticity of the endometrial stromal cell phenotype and suggest the possibility of acquired contractility by these cells in vivo and its potential contribution to uterine contractile activity. This phenomenon may be a typical example of how a tissue passively acquires new contractile functions under mechanical stimulation from a neighboring tissue, enabling it to support the adjacent tissue’s functions.
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spelling pubmed-72653712020-06-05 Acquired contractile ability in human endometrial stromal cells by passive loading of cyclic tensile stretch Kim, Jeonghyun Ushida, Takashi Montagne, Kevin Hirota, Yasushi Yoshino, Osamu Hiraoka, Takehiro Osuga, Yutaka Furuakwa, Katsuko S. Sci Rep Article The uterus plays an important and unique role during pregnancy and is a dynamic organ subjected to mechanical stimuli. It has been reported that infertility occurs when the peristalsis is prevented, although its mechanisms remain unknown. In this study, we found that mechanical strain mimicking the peristaltic motion of the uterine smooth muscle layer enabled the endometrial stromal cells to acquire contractility. In order to mimic the peristalsis induced by uterine smooth muscle cells, cyclic tensile stretch was applied to human endometrial stromal cells. The results showed that the strained cells exerted greater contractility in three-dimensional collagen gels in the presence of oxytocin, due to up-regulated alpha-smooth muscle actin expression via the cAMP signaling pathway. These in vitro findings underscore the plasticity of the endometrial stromal cell phenotype and suggest the possibility of acquired contractility by these cells in vivo and its potential contribution to uterine contractile activity. This phenomenon may be a typical example of how a tissue passively acquires new contractile functions under mechanical stimulation from a neighboring tissue, enabling it to support the adjacent tissue’s functions. Nature Publishing Group UK 2020-06-02 /pmc/articles/PMC7265371/ /pubmed/32488068 http://dx.doi.org/10.1038/s41598-020-65884-3 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kim, Jeonghyun
Ushida, Takashi
Montagne, Kevin
Hirota, Yasushi
Yoshino, Osamu
Hiraoka, Takehiro
Osuga, Yutaka
Furuakwa, Katsuko S.
Acquired contractile ability in human endometrial stromal cells by passive loading of cyclic tensile stretch
title Acquired contractile ability in human endometrial stromal cells by passive loading of cyclic tensile stretch
title_full Acquired contractile ability in human endometrial stromal cells by passive loading of cyclic tensile stretch
title_fullStr Acquired contractile ability in human endometrial stromal cells by passive loading of cyclic tensile stretch
title_full_unstemmed Acquired contractile ability in human endometrial stromal cells by passive loading of cyclic tensile stretch
title_short Acquired contractile ability in human endometrial stromal cells by passive loading of cyclic tensile stretch
title_sort acquired contractile ability in human endometrial stromal cells by passive loading of cyclic tensile stretch
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7265371/
https://www.ncbi.nlm.nih.gov/pubmed/32488068
http://dx.doi.org/10.1038/s41598-020-65884-3
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