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Oxidized alginate hydrogels as niche environments for corneal epithelial cells
Chemical and biochemical modification of hydrogels is one strategy to create physiological constructs that maintain cell function. The aim of this study was to apply oxidised alginate hydrogels as a basis for development of a biomimetic niche for limbal epithelial stem cells that may be applied to t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255301/ https://www.ncbi.nlm.nih.gov/pubmed/24142706 http://dx.doi.org/10.1002/jbm.a.35011 |
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author | Wright, Bernice De Bank, Paul A Luetchford, Kim A Acosta, Fernando R Connon, Che J |
author_facet | Wright, Bernice De Bank, Paul A Luetchford, Kim A Acosta, Fernando R Connon, Che J |
author_sort | Wright, Bernice |
collection | PubMed |
description | Chemical and biochemical modification of hydrogels is one strategy to create physiological constructs that maintain cell function. The aim of this study was to apply oxidised alginate hydrogels as a basis for development of a biomimetic niche for limbal epithelial stem cells that may be applied to treating corneal dysfunction. The stem phenotype of bovine limbal epithelial cells (LEC) and the viability of corneal epithelial cells (CEC) were examined in oxidised alginate gels containing collagen IV over a 3-day culture period. Oxidation increased cell viability (P ≤ 0.05) and this improved further with addition of collagen IV (P ≤ 0.01). Oxidised gels presented larger internal pores (diameter: 0.2–0.8 µm) than unmodified gels (pore diameter: 0.05–0.1 µm) and were significantly less stiff (P ≤ 0.001), indicating that an increase in pore size and a decrease in stiffness contributed to improved cell viability. The diffusion of collagen IV from oxidised alginate gels was similar to that of unmodified gels suggesting that oxidation may not affect the retention of extracellular matrix proteins in alginate gels. These data demonstrate that oxidised alginate gels containing corneal extracellular matrix proteins can influence corneal epithelial cell function in a manner that may impact beneficially on corneal wound healing therapy. © 2013 The Authors. Journal of Biomedical Materials Research Part A Published byWiley Periodicals, Inc. Part A: 102A: 3393–3400, 2014. |
format | Online Article Text |
id | pubmed-4255301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42553012014-12-08 Oxidized alginate hydrogels as niche environments for corneal epithelial cells Wright, Bernice De Bank, Paul A Luetchford, Kim A Acosta, Fernando R Connon, Che J J Biomed Mater Res A Original Articles Chemical and biochemical modification of hydrogels is one strategy to create physiological constructs that maintain cell function. The aim of this study was to apply oxidised alginate hydrogels as a basis for development of a biomimetic niche for limbal epithelial stem cells that may be applied to treating corneal dysfunction. The stem phenotype of bovine limbal epithelial cells (LEC) and the viability of corneal epithelial cells (CEC) were examined in oxidised alginate gels containing collagen IV over a 3-day culture period. Oxidation increased cell viability (P ≤ 0.05) and this improved further with addition of collagen IV (P ≤ 0.01). Oxidised gels presented larger internal pores (diameter: 0.2–0.8 µm) than unmodified gels (pore diameter: 0.05–0.1 µm) and were significantly less stiff (P ≤ 0.001), indicating that an increase in pore size and a decrease in stiffness contributed to improved cell viability. The diffusion of collagen IV from oxidised alginate gels was similar to that of unmodified gels suggesting that oxidation may not affect the retention of extracellular matrix proteins in alginate gels. These data demonstrate that oxidised alginate gels containing corneal extracellular matrix proteins can influence corneal epithelial cell function in a manner that may impact beneficially on corneal wound healing therapy. © 2013 The Authors. Journal of Biomedical Materials Research Part A Published byWiley Periodicals, Inc. Part A: 102A: 3393–3400, 2014. Blackwell Publishing Ltd 2014-10 2013-10-28 /pmc/articles/PMC4255301/ /pubmed/24142706 http://dx.doi.org/10.1002/jbm.a.35011 Text en © 2013 The Authors Journal of Biomedical Materials Research Part A Published by Wiley Periodicals, Inc. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Wright, Bernice De Bank, Paul A Luetchford, Kim A Acosta, Fernando R Connon, Che J Oxidized alginate hydrogels as niche environments for corneal epithelial cells |
title | Oxidized alginate hydrogels as niche environments for corneal epithelial cells |
title_full | Oxidized alginate hydrogels as niche environments for corneal epithelial cells |
title_fullStr | Oxidized alginate hydrogels as niche environments for corneal epithelial cells |
title_full_unstemmed | Oxidized alginate hydrogels as niche environments for corneal epithelial cells |
title_short | Oxidized alginate hydrogels as niche environments for corneal epithelial cells |
title_sort | oxidized alginate hydrogels as niche environments for corneal epithelial cells |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255301/ https://www.ncbi.nlm.nih.gov/pubmed/24142706 http://dx.doi.org/10.1002/jbm.a.35011 |
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