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Geometric constraints of endothelial cell migration on electrospun fibres
Biomaterial scaffolds that can form a template for tissue growth and repair forms the basis of many tissue engineering paradigms. Cell migration and colonisation is an important, and often overlooked, first step. In this study, fibrous guidance structures were produced via electrospinning and the ef...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913261/ https://www.ncbi.nlm.nih.gov/pubmed/29686428 http://dx.doi.org/10.1038/s41598-018-24667-7 |
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author | Ahmed, Maqsood Ramos, Tiago Wieringa, Paul Blitterswijk, Clemens van Boer, Jan de Moroni, Lorenzo |
author_facet | Ahmed, Maqsood Ramos, Tiago Wieringa, Paul Blitterswijk, Clemens van Boer, Jan de Moroni, Lorenzo |
author_sort | Ahmed, Maqsood |
collection | PubMed |
description | Biomaterial scaffolds that can form a template for tissue growth and repair forms the basis of many tissue engineering paradigms. Cell migration and colonisation is an important, and often overlooked, first step. In this study, fibrous guidance structures were produced via electrospinning and the effect of physical features such as fibre diameter (ranging from 500 nm to 10 μm) on endothelial cell migration was assessed. Using a modified wound healing assay, fibre diameter was found to have a significant effect on the rate of wound closure and the peak migration velocity of the cells with scaffold diameter shown to influence both morphology and alignment of the migrating cells. The expression, phosphorylation and distribution of focal adhesion kinase (FAK) was disrupted on the different scaffolds with small-diameter scaffolds exhibiting increased FAK phosphorylation with the kinase present in the cytosol whereas on large-diameter scaffolds FAK was largely restricted to focal adhesions at the cell periphery. This study demonstrates that electrospun scaffolds can be used to model cell migration on fibrous substrates, and particularly for the studying effects of physical features of the substrate, and that FAK is a key mediator of cell-scaffold interactions on migrating cells. |
format | Online Article Text |
id | pubmed-5913261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59132612018-04-30 Geometric constraints of endothelial cell migration on electrospun fibres Ahmed, Maqsood Ramos, Tiago Wieringa, Paul Blitterswijk, Clemens van Boer, Jan de Moroni, Lorenzo Sci Rep Article Biomaterial scaffolds that can form a template for tissue growth and repair forms the basis of many tissue engineering paradigms. Cell migration and colonisation is an important, and often overlooked, first step. In this study, fibrous guidance structures were produced via electrospinning and the effect of physical features such as fibre diameter (ranging from 500 nm to 10 μm) on endothelial cell migration was assessed. Using a modified wound healing assay, fibre diameter was found to have a significant effect on the rate of wound closure and the peak migration velocity of the cells with scaffold diameter shown to influence both morphology and alignment of the migrating cells. The expression, phosphorylation and distribution of focal adhesion kinase (FAK) was disrupted on the different scaffolds with small-diameter scaffolds exhibiting increased FAK phosphorylation with the kinase present in the cytosol whereas on large-diameter scaffolds FAK was largely restricted to focal adhesions at the cell periphery. This study demonstrates that electrospun scaffolds can be used to model cell migration on fibrous substrates, and particularly for the studying effects of physical features of the substrate, and that FAK is a key mediator of cell-scaffold interactions on migrating cells. Nature Publishing Group UK 2018-04-23 /pmc/articles/PMC5913261/ /pubmed/29686428 http://dx.doi.org/10.1038/s41598-018-24667-7 Text en © The Author(s) 2018 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/. |
spellingShingle | Article Ahmed, Maqsood Ramos, Tiago Wieringa, Paul Blitterswijk, Clemens van Boer, Jan de Moroni, Lorenzo Geometric constraints of endothelial cell migration on electrospun fibres |
title | Geometric constraints of endothelial cell migration on electrospun fibres |
title_full | Geometric constraints of endothelial cell migration on electrospun fibres |
title_fullStr | Geometric constraints of endothelial cell migration on electrospun fibres |
title_full_unstemmed | Geometric constraints of endothelial cell migration on electrospun fibres |
title_short | Geometric constraints of endothelial cell migration on electrospun fibres |
title_sort | geometric constraints of endothelial cell migration on electrospun fibres |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913261/ https://www.ncbi.nlm.nih.gov/pubmed/29686428 http://dx.doi.org/10.1038/s41598-018-24667-7 |
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