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ROCK inhibitor combined with Ca(2+) controls the myosin II activation and optimizes human nasal epithelial cell sheets
The proliferation and differentiation of cultured epithelial cells may be modified by Rho-associated kinase (ROCK) inhibition and extracellular Ca(2+) concentration. However, it was not known whether a combination would influence the behavior of cultured epithelial cells through changes in the phosp...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7544873/ https://www.ncbi.nlm.nih.gov/pubmed/33033339 http://dx.doi.org/10.1038/s41598-020-73817-3 |
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author | Kasai, Yoshiyuki Morino, Tsunetaro Mori, Eri Yamamoto, Kazuhisa Kojima, Hiromi |
author_facet | Kasai, Yoshiyuki Morino, Tsunetaro Mori, Eri Yamamoto, Kazuhisa Kojima, Hiromi |
author_sort | Kasai, Yoshiyuki |
collection | PubMed |
description | The proliferation and differentiation of cultured epithelial cells may be modified by Rho-associated kinase (ROCK) inhibition and extracellular Ca(2+) concentration. However, it was not known whether a combination would influence the behavior of cultured epithelial cells through changes in the phosphorylation of non-muscle myosin light chain II (MLC). Here we show that the combination of ROCK inhibition with Ca(2+) elevation regulated the phosphorylation of MLC and improved both cell expansion and cell–cell adhesion during the culture of human nasal mucosal epithelial cell sheets. During explant culture, Ca(2+) enhanced the adhesion of nasal mucosal tissue, while ROCK inhibition downregulated MLC phosphorylation and promoted cell proliferation. During cell sheet culture, an elevation of extracellular Ca(2+) promoted MLC phosphorylation and formation of cell–cell junctions, allowing the harvesting of cell sheets without collapse. Moreover, an in vitro grafting assay revealed that ROCK inhibition increased the expansion of cell sheets three-fold (an effect maintained when Ca(2+) was also elevated), implying better wound healing potential. We suggest that combining ROCK inhibition with elevation of Ca(2+) could facilitate the fabrication of many types of cell graft. |
format | Online Article Text |
id | pubmed-7544873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75448732020-10-14 ROCK inhibitor combined with Ca(2+) controls the myosin II activation and optimizes human nasal epithelial cell sheets Kasai, Yoshiyuki Morino, Tsunetaro Mori, Eri Yamamoto, Kazuhisa Kojima, Hiromi Sci Rep Article The proliferation and differentiation of cultured epithelial cells may be modified by Rho-associated kinase (ROCK) inhibition and extracellular Ca(2+) concentration. However, it was not known whether a combination would influence the behavior of cultured epithelial cells through changes in the phosphorylation of non-muscle myosin light chain II (MLC). Here we show that the combination of ROCK inhibition with Ca(2+) elevation regulated the phosphorylation of MLC and improved both cell expansion and cell–cell adhesion during the culture of human nasal mucosal epithelial cell sheets. During explant culture, Ca(2+) enhanced the adhesion of nasal mucosal tissue, while ROCK inhibition downregulated MLC phosphorylation and promoted cell proliferation. During cell sheet culture, an elevation of extracellular Ca(2+) promoted MLC phosphorylation and formation of cell–cell junctions, allowing the harvesting of cell sheets without collapse. Moreover, an in vitro grafting assay revealed that ROCK inhibition increased the expansion of cell sheets three-fold (an effect maintained when Ca(2+) was also elevated), implying better wound healing potential. We suggest that combining ROCK inhibition with elevation of Ca(2+) could facilitate the fabrication of many types of cell graft. Nature Publishing Group UK 2020-10-08 /pmc/articles/PMC7544873/ /pubmed/33033339 http://dx.doi.org/10.1038/s41598-020-73817-3 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 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/. |
spellingShingle | Article Kasai, Yoshiyuki Morino, Tsunetaro Mori, Eri Yamamoto, Kazuhisa Kojima, Hiromi ROCK inhibitor combined with Ca(2+) controls the myosin II activation and optimizes human nasal epithelial cell sheets |
title | ROCK inhibitor combined with Ca(2+) controls the myosin II activation and optimizes human nasal epithelial cell sheets |
title_full | ROCK inhibitor combined with Ca(2+) controls the myosin II activation and optimizes human nasal epithelial cell sheets |
title_fullStr | ROCK inhibitor combined with Ca(2+) controls the myosin II activation and optimizes human nasal epithelial cell sheets |
title_full_unstemmed | ROCK inhibitor combined with Ca(2+) controls the myosin II activation and optimizes human nasal epithelial cell sheets |
title_short | ROCK inhibitor combined with Ca(2+) controls the myosin II activation and optimizes human nasal epithelial cell sheets |
title_sort | rock inhibitor combined with ca(2+) controls the myosin ii activation and optimizes human nasal epithelial cell sheets |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7544873/ https://www.ncbi.nlm.nih.gov/pubmed/33033339 http://dx.doi.org/10.1038/s41598-020-73817-3 |
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