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Epithelial cells sacrifice excess area to preserve fluidity in response to external mechanical stress
Viscoelastic properties of epithelial cells subject to shape changes were monitored by indentation-retraction/relaxation experiments. MDCK II cells cultured on extensible polydimethylsiloxane substrates were laterally stretched and, in response, displayed increased cortex contractility and loss of e...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395404/ https://www.ncbi.nlm.nih.gov/pubmed/35995827 http://dx.doi.org/10.1038/s42003-022-03809-8 |
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author | Bodenschatz, Jonathan F. E. Ajmail, Karim Skamrahl, Mark Vache, Marian Gottwald, Jannis Nehls, Stefan Janshoff, Andreas |
author_facet | Bodenschatz, Jonathan F. E. Ajmail, Karim Skamrahl, Mark Vache, Marian Gottwald, Jannis Nehls, Stefan Janshoff, Andreas |
author_sort | Bodenschatz, Jonathan F. E. |
collection | PubMed |
description | Viscoelastic properties of epithelial cells subject to shape changes were monitored by indentation-retraction/relaxation experiments. MDCK II cells cultured on extensible polydimethylsiloxane substrates were laterally stretched and, in response, displayed increased cortex contractility and loss of excess surface area. Thereby, the cells preserve their fluidity but inevitably become stiffer. We found similar behavior in demixed cell monolayers of ZO-1/2 double knock down (dKD) cells, cells exposed to different temperatures and after removal of cholesterol from the plasma membrane. Conversely, the mechanical response of single cells adhered onto differently sized patches displays no visible rheological change. Sacrificing excess surface area allows the cells to respond to mechanical challenges without losing their ability to flow. They gain a new degree of freedom that permits resolving the interdependence of fluidity β on stiffness [Formula: see text] . We also propose a model that permits to tell apart contributions from excess membrane area and excess cell surface area. |
format | Online Article Text |
id | pubmed-9395404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-93954042022-08-24 Epithelial cells sacrifice excess area to preserve fluidity in response to external mechanical stress Bodenschatz, Jonathan F. E. Ajmail, Karim Skamrahl, Mark Vache, Marian Gottwald, Jannis Nehls, Stefan Janshoff, Andreas Commun Biol Article Viscoelastic properties of epithelial cells subject to shape changes were monitored by indentation-retraction/relaxation experiments. MDCK II cells cultured on extensible polydimethylsiloxane substrates were laterally stretched and, in response, displayed increased cortex contractility and loss of excess surface area. Thereby, the cells preserve their fluidity but inevitably become stiffer. We found similar behavior in demixed cell monolayers of ZO-1/2 double knock down (dKD) cells, cells exposed to different temperatures and after removal of cholesterol from the plasma membrane. Conversely, the mechanical response of single cells adhered onto differently sized patches displays no visible rheological change. Sacrificing excess surface area allows the cells to respond to mechanical challenges without losing their ability to flow. They gain a new degree of freedom that permits resolving the interdependence of fluidity β on stiffness [Formula: see text] . We also propose a model that permits to tell apart contributions from excess membrane area and excess cell surface area. Nature Publishing Group UK 2022-08-22 /pmc/articles/PMC9395404/ /pubmed/35995827 http://dx.doi.org/10.1038/s42003-022-03809-8 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Bodenschatz, Jonathan F. E. Ajmail, Karim Skamrahl, Mark Vache, Marian Gottwald, Jannis Nehls, Stefan Janshoff, Andreas Epithelial cells sacrifice excess area to preserve fluidity in response to external mechanical stress |
title | Epithelial cells sacrifice excess area to preserve fluidity in response to external mechanical stress |
title_full | Epithelial cells sacrifice excess area to preserve fluidity in response to external mechanical stress |
title_fullStr | Epithelial cells sacrifice excess area to preserve fluidity in response to external mechanical stress |
title_full_unstemmed | Epithelial cells sacrifice excess area to preserve fluidity in response to external mechanical stress |
title_short | Epithelial cells sacrifice excess area to preserve fluidity in response to external mechanical stress |
title_sort | epithelial cells sacrifice excess area to preserve fluidity in response to external mechanical stress |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395404/ https://www.ncbi.nlm.nih.gov/pubmed/35995827 http://dx.doi.org/10.1038/s42003-022-03809-8 |
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