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Azobenzene-based sinusoidal surface topography drives focal adhesion confinement and guides collective migration of epithelial cells

Surface topography is a key parameter in regulating the morphology and behavior of single cells. At multicellular level, coordinated cell displacements drive many biological events such as embryonic morphogenesis. However, the effect of surface topography on collective migration of epithelium has no...

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Autores principales: Fedele, Chiara, Mäntylä, Elina, Belardi, Brian, Hamkins-Indik, Tiama, Cavalli, Silvia, Netti, Paolo A., Fletcher, Daniel A., Nymark, Soile, Priimagi, Arri, Ihalainen, Teemu O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501301/
https://www.ncbi.nlm.nih.gov/pubmed/32948792
http://dx.doi.org/10.1038/s41598-020-71567-w
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author Fedele, Chiara
Mäntylä, Elina
Belardi, Brian
Hamkins-Indik, Tiama
Cavalli, Silvia
Netti, Paolo A.
Fletcher, Daniel A.
Nymark, Soile
Priimagi, Arri
Ihalainen, Teemu O.
author_facet Fedele, Chiara
Mäntylä, Elina
Belardi, Brian
Hamkins-Indik, Tiama
Cavalli, Silvia
Netti, Paolo A.
Fletcher, Daniel A.
Nymark, Soile
Priimagi, Arri
Ihalainen, Teemu O.
author_sort Fedele, Chiara
collection PubMed
description Surface topography is a key parameter in regulating the morphology and behavior of single cells. At multicellular level, coordinated cell displacements drive many biological events such as embryonic morphogenesis. However, the effect of surface topography on collective migration of epithelium has not been studied in detail. Mastering the connection between surface features and collective cellular behaviour is highly important for novel approaches in tissue engineering and repair. Herein, we used photopatterned microtopographies on azobenzene-containing materials and showed that smooth topographical cues with proper period and orientation can efficiently orchestrate cell alignment in growing epithelium. Furthermore, the experimental system allowed us to investigate how the orientation of the topographical features can alter the speed of wound closure in vitro. Our findings indicate that the extracellular microenvironment topography coordinates their focal adhesion distribution and alignment. These topographic cues are able to guide the collective migration of multicellular systems, even when cell–cell junctions are disrupted.
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spelling pubmed-75013012020-09-22 Azobenzene-based sinusoidal surface topography drives focal adhesion confinement and guides collective migration of epithelial cells Fedele, Chiara Mäntylä, Elina Belardi, Brian Hamkins-Indik, Tiama Cavalli, Silvia Netti, Paolo A. Fletcher, Daniel A. Nymark, Soile Priimagi, Arri Ihalainen, Teemu O. Sci Rep Article Surface topography is a key parameter in regulating the morphology and behavior of single cells. At multicellular level, coordinated cell displacements drive many biological events such as embryonic morphogenesis. However, the effect of surface topography on collective migration of epithelium has not been studied in detail. Mastering the connection between surface features and collective cellular behaviour is highly important for novel approaches in tissue engineering and repair. Herein, we used photopatterned microtopographies on azobenzene-containing materials and showed that smooth topographical cues with proper period and orientation can efficiently orchestrate cell alignment in growing epithelium. Furthermore, the experimental system allowed us to investigate how the orientation of the topographical features can alter the speed of wound closure in vitro. Our findings indicate that the extracellular microenvironment topography coordinates their focal adhesion distribution and alignment. These topographic cues are able to guide the collective migration of multicellular systems, even when cell–cell junctions are disrupted. Nature Publishing Group UK 2020-09-18 /pmc/articles/PMC7501301/ /pubmed/32948792 http://dx.doi.org/10.1038/s41598-020-71567-w 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
Fedele, Chiara
Mäntylä, Elina
Belardi, Brian
Hamkins-Indik, Tiama
Cavalli, Silvia
Netti, Paolo A.
Fletcher, Daniel A.
Nymark, Soile
Priimagi, Arri
Ihalainen, Teemu O.
Azobenzene-based sinusoidal surface topography drives focal adhesion confinement and guides collective migration of epithelial cells
title Azobenzene-based sinusoidal surface topography drives focal adhesion confinement and guides collective migration of epithelial cells
title_full Azobenzene-based sinusoidal surface topography drives focal adhesion confinement and guides collective migration of epithelial cells
title_fullStr Azobenzene-based sinusoidal surface topography drives focal adhesion confinement and guides collective migration of epithelial cells
title_full_unstemmed Azobenzene-based sinusoidal surface topography drives focal adhesion confinement and guides collective migration of epithelial cells
title_short Azobenzene-based sinusoidal surface topography drives focal adhesion confinement and guides collective migration of epithelial cells
title_sort azobenzene-based sinusoidal surface topography drives focal adhesion confinement and guides collective migration of epithelial cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501301/
https://www.ncbi.nlm.nih.gov/pubmed/32948792
http://dx.doi.org/10.1038/s41598-020-71567-w
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