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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...

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Autores principales: Pramotton, Francesca Michela, Cousin, Lucien, Roy, Tamal, Giampietro, Costanza, Cecchini, Marco, Masciullo, Cecilia, Ferrari, Aldo, Poulikakos, Dimos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
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.
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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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