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Influence of culture conditions and extracellular matrix alignment on human mesenchymal stem cells invasion into decellularized engineered tissues

The variables that influence the in vitro recellularization potential of decellularized engineered tissues, such as cell culture conditions and scaffold alignment, have yet to be explored. The goal of this work was to explore the influence of insulin and ascorbic acid and extracellular matrix (ECM)...

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Autores principales: Weidenhamer, Nathan K., Moore, Dusty L., Lobo, Fluvio L., Klair, Nathaniel T., Tranquillo, Robert T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4409517/
https://www.ncbi.nlm.nih.gov/pubmed/25556358
http://dx.doi.org/10.1002/term.1974
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author Weidenhamer, Nathan K.
Moore, Dusty L.
Lobo, Fluvio L.
Klair, Nathaniel T.
Tranquillo, Robert T.
author_facet Weidenhamer, Nathan K.
Moore, Dusty L.
Lobo, Fluvio L.
Klair, Nathaniel T.
Tranquillo, Robert T.
author_sort Weidenhamer, Nathan K.
collection PubMed
description The variables that influence the in vitro recellularization potential of decellularized engineered tissues, such as cell culture conditions and scaffold alignment, have yet to be explored. The goal of this work was to explore the influence of insulin and ascorbic acid and extracellular matrix (ECM) alignment on the recellularization of decellularized engineered tissue by human mesenchymal stem cells (hMSCs). Aligned and non‐aligned tissues were created by specifying the geometry and associated mechanical constraints to fibroblast‐mediated fibrin gel contraction and remodelling using circular and C‐shaped moulds. Decellularized tissues (matrices) of the same alignment were created by decellularization with detergents. Ascorbic acid promoted the invasion of hMSCs into the matrices due to a stimulated increase in motility and proliferation. Invasion correlated with hyaluronic acid secretion, α‐smooth muscle actin expression and decreased matrix thickness. Furthermore, hMSCs invasion into aligned and non‐aligned matrices was not different, although there was a difference in cell orientation. Finally, we show that hMSCs on the matrix surface appear to differentiate toward a smooth muscle cell or myofibroblast phenotype with ascorbic acid treatment. These results inform the strategy of recellularizing decellularized engineered tissue with hMSCs. © 2015 The Authors Journal of Tissue Engineering and Regenerative Medicine Published by John Wiley & Sons Ltd.
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spelling pubmed-44095172016-05-01 Influence of culture conditions and extracellular matrix alignment on human mesenchymal stem cells invasion into decellularized engineered tissues Weidenhamer, Nathan K. Moore, Dusty L. Lobo, Fluvio L. Klair, Nathaniel T. Tranquillo, Robert T. J Tissue Eng Regen Med Research Articles The variables that influence the in vitro recellularization potential of decellularized engineered tissues, such as cell culture conditions and scaffold alignment, have yet to be explored. The goal of this work was to explore the influence of insulin and ascorbic acid and extracellular matrix (ECM) alignment on the recellularization of decellularized engineered tissue by human mesenchymal stem cells (hMSCs). Aligned and non‐aligned tissues were created by specifying the geometry and associated mechanical constraints to fibroblast‐mediated fibrin gel contraction and remodelling using circular and C‐shaped moulds. Decellularized tissues (matrices) of the same alignment were created by decellularization with detergents. Ascorbic acid promoted the invasion of hMSCs into the matrices due to a stimulated increase in motility and proliferation. Invasion correlated with hyaluronic acid secretion, α‐smooth muscle actin expression and decreased matrix thickness. Furthermore, hMSCs invasion into aligned and non‐aligned matrices was not different, although there was a difference in cell orientation. Finally, we show that hMSCs on the matrix surface appear to differentiate toward a smooth muscle cell or myofibroblast phenotype with ascorbic acid treatment. These results inform the strategy of recellularizing decellularized engineered tissue with hMSCs. © 2015 The Authors Journal of Tissue Engineering and Regenerative Medicine Published by John Wiley & Sons Ltd. John Wiley and Sons Inc. 2015-01-02 2015-05 /pmc/articles/PMC4409517/ /pubmed/25556358 http://dx.doi.org/10.1002/term.1974 Text en © 2015 The Authors Journal of Tissue Engineering and Regenerative Medicine Published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Weidenhamer, Nathan K.
Moore, Dusty L.
Lobo, Fluvio L.
Klair, Nathaniel T.
Tranquillo, Robert T.
Influence of culture conditions and extracellular matrix alignment on human mesenchymal stem cells invasion into decellularized engineered tissues
title Influence of culture conditions and extracellular matrix alignment on human mesenchymal stem cells invasion into decellularized engineered tissues
title_full Influence of culture conditions and extracellular matrix alignment on human mesenchymal stem cells invasion into decellularized engineered tissues
title_fullStr Influence of culture conditions and extracellular matrix alignment on human mesenchymal stem cells invasion into decellularized engineered tissues
title_full_unstemmed Influence of culture conditions and extracellular matrix alignment on human mesenchymal stem cells invasion into decellularized engineered tissues
title_short Influence of culture conditions and extracellular matrix alignment on human mesenchymal stem cells invasion into decellularized engineered tissues
title_sort influence of culture conditions and extracellular matrix alignment on human mesenchymal stem cells invasion into decellularized engineered tissues
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4409517/
https://www.ncbi.nlm.nih.gov/pubmed/25556358
http://dx.doi.org/10.1002/term.1974
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