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A methodology for the production of microfabricated electrospun membranes for the creation of new skin regeneration models

The continual renewal of the epidermis is thought to be related to the presence of populations of epidermal stem cells residing in physically protected microenvironments (rete ridges) directly influenced by the presence of mesenchymal fibroblasts. Current skin in vitro models do acknowledge the infl...

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Autores principales: Asencio, Ilida Ortega, Mittar, Shweta, Sherborne, Colin, Raza, Ahtasham, Claeyssens, Frederik, MacNeil, Sheila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6153546/
https://www.ncbi.nlm.nih.gov/pubmed/30263105
http://dx.doi.org/10.1177/2041731418799851
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author Asencio, Ilida Ortega
Mittar, Shweta
Sherborne, Colin
Raza, Ahtasham
Claeyssens, Frederik
MacNeil, Sheila
author_facet Asencio, Ilida Ortega
Mittar, Shweta
Sherborne, Colin
Raza, Ahtasham
Claeyssens, Frederik
MacNeil, Sheila
author_sort Asencio, Ilida Ortega
collection PubMed
description The continual renewal of the epidermis is thought to be related to the presence of populations of epidermal stem cells residing in physically protected microenvironments (rete ridges) directly influenced by the presence of mesenchymal fibroblasts. Current skin in vitro models do acknowledge the influence of stromal fibroblasts in skin reorganisation but the study of the effect of the rete ridge-microenvironment on epidermal renewal still remains a rich topic for exploration. We suggest there is a need for the development of new in vitro models in which to study epithelial stem cell behaviour prior to translating these models into the design of new cell-free biomaterial devices for skin reconstruction. In this study, we aimed to develop new prototype epidermal-like layers containing pseudo-rete ridge structures for studying the effect of topographical cues on epithelial cell behaviour. The models were designed using a range of three-dimensional electrospun microfabricated scaffolds. This was achieved via the utilisation of polyethylene glycol diacrylate to produce a reusable template over which poly(3-hydrroxybutyrate-co-3-hydroxyvalerate) was electrospun. Initial investigations studied the behaviour of keratinocytes cultured on models using plain scaffolds (without the presence of intricate topography) versus keratinocytes cultured on scaffolds containing microfeatures.
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spelling pubmed-61535462018-09-27 A methodology for the production of microfabricated electrospun membranes for the creation of new skin regeneration models Asencio, Ilida Ortega Mittar, Shweta Sherborne, Colin Raza, Ahtasham Claeyssens, Frederik MacNeil, Sheila J Tissue Eng Acellular Approaches for Regenerative Medicine: Driving Biology without the Cell The continual renewal of the epidermis is thought to be related to the presence of populations of epidermal stem cells residing in physically protected microenvironments (rete ridges) directly influenced by the presence of mesenchymal fibroblasts. Current skin in vitro models do acknowledge the influence of stromal fibroblasts in skin reorganisation but the study of the effect of the rete ridge-microenvironment on epidermal renewal still remains a rich topic for exploration. We suggest there is a need for the development of new in vitro models in which to study epithelial stem cell behaviour prior to translating these models into the design of new cell-free biomaterial devices for skin reconstruction. In this study, we aimed to develop new prototype epidermal-like layers containing pseudo-rete ridge structures for studying the effect of topographical cues on epithelial cell behaviour. The models were designed using a range of three-dimensional electrospun microfabricated scaffolds. This was achieved via the utilisation of polyethylene glycol diacrylate to produce a reusable template over which poly(3-hydrroxybutyrate-co-3-hydroxyvalerate) was electrospun. Initial investigations studied the behaviour of keratinocytes cultured on models using plain scaffolds (without the presence of intricate topography) versus keratinocytes cultured on scaffolds containing microfeatures. SAGE Publications 2018-09-21 /pmc/articles/PMC6153546/ /pubmed/30263105 http://dx.doi.org/10.1177/2041731418799851 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 License (http://www.creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Acellular Approaches for Regenerative Medicine: Driving Biology without the Cell
Asencio, Ilida Ortega
Mittar, Shweta
Sherborne, Colin
Raza, Ahtasham
Claeyssens, Frederik
MacNeil, Sheila
A methodology for the production of microfabricated electrospun membranes for the creation of new skin regeneration models
title A methodology for the production of microfabricated electrospun membranes for the creation of new skin regeneration models
title_full A methodology for the production of microfabricated electrospun membranes for the creation of new skin regeneration models
title_fullStr A methodology for the production of microfabricated electrospun membranes for the creation of new skin regeneration models
title_full_unstemmed A methodology for the production of microfabricated electrospun membranes for the creation of new skin regeneration models
title_short A methodology for the production of microfabricated electrospun membranes for the creation of new skin regeneration models
title_sort methodology for the production of microfabricated electrospun membranes for the creation of new skin regeneration models
topic Acellular Approaches for Regenerative Medicine: Driving Biology without the Cell
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6153546/
https://www.ncbi.nlm.nih.gov/pubmed/30263105
http://dx.doi.org/10.1177/2041731418799851
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