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Asymmetrical seeding of MSCs into fibrin–poly(ester‐urethane) scaffolds and its effect on mechanically induced chondrogenesis

Mesenchymal stem cells (MSCs) are currently being investigated as candidate cells for regenerative medicine approaches for the repair of damaged articular cartilage. For these cells to be used clinically, it is important to understand how they will react to the complex loading environment of a joint...

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Autores principales: Gardner, Oliver F. W., Musumeci, Giuseppe, Neumann, Alexander J., Eglin, David, Archer, Charles W., Alini, Mauro, Stoddart, Martin J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093257/
https://www.ncbi.nlm.nih.gov/pubmed/27406210
http://dx.doi.org/10.1002/term.2194
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author Gardner, Oliver F. W.
Musumeci, Giuseppe
Neumann, Alexander J.
Eglin, David
Archer, Charles W.
Alini, Mauro
Stoddart, Martin J.
author_facet Gardner, Oliver F. W.
Musumeci, Giuseppe
Neumann, Alexander J.
Eglin, David
Archer, Charles W.
Alini, Mauro
Stoddart, Martin J.
author_sort Gardner, Oliver F. W.
collection PubMed
description Mesenchymal stem cells (MSCs) are currently being investigated as candidate cells for regenerative medicine approaches for the repair of damaged articular cartilage. For these cells to be used clinically, it is important to understand how they will react to the complex loading environment of a joint in vivo. In addition to investigating alternative cell sources, it is also important for the structure of tissue‐engineered constructs and the organization of cells within them to be developed and, if possible, improved. A custom built bioreactor was used to expose human MSCs to a combination of shear and compression loading. The MSCs were either evenly distributed throughout fibrin‐poly(ester‐urethane) scaffolds or asymmetrically seeded with a small proportion seeded on the surface of the scaffold. The effect of cell distribution on the production and deposition of cartilage‐like matrix in response to mechanical load mimicking in vivo joint loading was then investigated. The results show that asymmetrically seeding the scaffold led to markedly improved tissue development based on histologically detectable matrix deposition. Consideration of cell location, therefore, is an important aspect in the development of regenerative medicine approaches for cartilage repair. This is particularly relevant when considering the natural biomechanical environment of the joint in vivo and patient rehabilitation protocols. © 2016 The Authors Journal of Tissue Engineering and Regenerative Medicine Published by John Wiley & Sons Ltd.
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spelling pubmed-60932572018-08-20 Asymmetrical seeding of MSCs into fibrin–poly(ester‐urethane) scaffolds and its effect on mechanically induced chondrogenesis Gardner, Oliver F. W. Musumeci, Giuseppe Neumann, Alexander J. Eglin, David Archer, Charles W. Alini, Mauro Stoddart, Martin J. J Tissue Eng Regen Med Research Articles Mesenchymal stem cells (MSCs) are currently being investigated as candidate cells for regenerative medicine approaches for the repair of damaged articular cartilage. For these cells to be used clinically, it is important to understand how they will react to the complex loading environment of a joint in vivo. In addition to investigating alternative cell sources, it is also important for the structure of tissue‐engineered constructs and the organization of cells within them to be developed and, if possible, improved. A custom built bioreactor was used to expose human MSCs to a combination of shear and compression loading. The MSCs were either evenly distributed throughout fibrin‐poly(ester‐urethane) scaffolds or asymmetrically seeded with a small proportion seeded on the surface of the scaffold. The effect of cell distribution on the production and deposition of cartilage‐like matrix in response to mechanical load mimicking in vivo joint loading was then investigated. The results show that asymmetrically seeding the scaffold led to markedly improved tissue development based on histologically detectable matrix deposition. Consideration of cell location, therefore, is an important aspect in the development of regenerative medicine approaches for cartilage repair. This is particularly relevant when considering the natural biomechanical environment of the joint in vivo and patient rehabilitation protocols. © 2016 The Authors Journal of Tissue Engineering and Regenerative Medicine Published by John Wiley & Sons Ltd. John Wiley and Sons Inc. 2016-07-13 2017-10 /pmc/articles/PMC6093257/ /pubmed/27406210 http://dx.doi.org/10.1002/term.2194 Text en © 2016 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/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Gardner, Oliver F. W.
Musumeci, Giuseppe
Neumann, Alexander J.
Eglin, David
Archer, Charles W.
Alini, Mauro
Stoddart, Martin J.
Asymmetrical seeding of MSCs into fibrin–poly(ester‐urethane) scaffolds and its effect on mechanically induced chondrogenesis
title Asymmetrical seeding of MSCs into fibrin–poly(ester‐urethane) scaffolds and its effect on mechanically induced chondrogenesis
title_full Asymmetrical seeding of MSCs into fibrin–poly(ester‐urethane) scaffolds and its effect on mechanically induced chondrogenesis
title_fullStr Asymmetrical seeding of MSCs into fibrin–poly(ester‐urethane) scaffolds and its effect on mechanically induced chondrogenesis
title_full_unstemmed Asymmetrical seeding of MSCs into fibrin–poly(ester‐urethane) scaffolds and its effect on mechanically induced chondrogenesis
title_short Asymmetrical seeding of MSCs into fibrin–poly(ester‐urethane) scaffolds and its effect on mechanically induced chondrogenesis
title_sort asymmetrical seeding of mscs into fibrin–poly(ester‐urethane) scaffolds and its effect on mechanically induced chondrogenesis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093257/
https://www.ncbi.nlm.nih.gov/pubmed/27406210
http://dx.doi.org/10.1002/term.2194
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