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Accelerated epithelial layer healing induced by tactile anisotropy in surface topography
Mammalian cells respond to tactile cues from topographic elements presented by the substrate. Among these, anisotropic features distributed in an ordered manner give directionality. In the extracellular matrix, this ordering is embedded in a noisy environment altering the contact guidance effect. To...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081848/ https://www.ncbi.nlm.nih.gov/pubmed/37027475 http://dx.doi.org/10.1126/sciadv.add1581 |
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author | Pramotton, Francesca Michela Cousin, Lucien Roy, Tamal Giampietro, Costanza Cecchini, Marco Masciullo, Cecilia Ferrari, Aldo Poulikakos, Dimos |
author_facet | Pramotton, Francesca Michela Cousin, Lucien Roy, Tamal Giampietro, Costanza Cecchini, Marco Masciullo, Cecilia Ferrari, Aldo Poulikakos, Dimos |
author_sort | Pramotton, Francesca Michela |
collection | PubMed |
description | Mammalian cells respond to tactile cues from topographic elements presented by the substrate. Among these, anisotropic features distributed in an ordered manner give directionality. In the extracellular matrix, this ordering is embedded in a noisy environment altering the contact guidance effect. To date, it is unclear how cells respond to topographical signals in a noisy environment. Here, using rationally designed substrates, we report morphotaxis, a guidance mechanism enabling fibroblasts and epithelial cells to move along gradients of topographic order distortion. Isolated cells and cell ensembles perform morphotaxis in response to gradients of different strength and directionality, with mature epithelia integrating variations of topographic order over hundreds of micrometers. The level of topographic order controls cell cycle progression, locally delaying or promoting cell proliferation. In mature epithelia, the combination of morphotaxis and noise-dependent distributed proliferation provides a strategy to enhance wound healing as confirmed by a mathematical model capturing key elements of the process. |
format | Online Article Text |
id | pubmed-10081848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-100818482023-04-08 Accelerated epithelial layer healing induced by tactile anisotropy in surface topography Pramotton, Francesca Michela Cousin, Lucien Roy, Tamal Giampietro, Costanza Cecchini, Marco Masciullo, Cecilia Ferrari, Aldo Poulikakos, Dimos Sci Adv Biomedicine and Life Sciences Mammalian cells respond to tactile cues from topographic elements presented by the substrate. Among these, anisotropic features distributed in an ordered manner give directionality. In the extracellular matrix, this ordering is embedded in a noisy environment altering the contact guidance effect. To date, it is unclear how cells respond to topographical signals in a noisy environment. Here, using rationally designed substrates, we report morphotaxis, a guidance mechanism enabling fibroblasts and epithelial cells to move along gradients of topographic order distortion. Isolated cells and cell ensembles perform morphotaxis in response to gradients of different strength and directionality, with mature epithelia integrating variations of topographic order over hundreds of micrometers. The level of topographic order controls cell cycle progression, locally delaying or promoting cell proliferation. In mature epithelia, the combination of morphotaxis and noise-dependent distributed proliferation provides a strategy to enhance wound healing as confirmed by a mathematical model capturing key elements of the process. American Association for the Advancement of Science 2023-04-07 /pmc/articles/PMC10081848/ /pubmed/37027475 http://dx.doi.org/10.1126/sciadv.add1581 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Pramotton, Francesca Michela Cousin, Lucien Roy, Tamal Giampietro, Costanza Cecchini, Marco Masciullo, Cecilia Ferrari, Aldo Poulikakos, Dimos Accelerated epithelial layer healing induced by tactile anisotropy in surface topography |
title | Accelerated epithelial layer healing induced by tactile anisotropy in surface topography |
title_full | Accelerated epithelial layer healing induced by tactile anisotropy in surface topography |
title_fullStr | Accelerated epithelial layer healing induced by tactile anisotropy in surface topography |
title_full_unstemmed | Accelerated epithelial layer healing induced by tactile anisotropy in surface topography |
title_short | Accelerated epithelial layer healing induced by tactile anisotropy in surface topography |
title_sort | accelerated epithelial layer healing induced by tactile anisotropy in surface topography |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081848/ https://www.ncbi.nlm.nih.gov/pubmed/37027475 http://dx.doi.org/10.1126/sciadv.add1581 |
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