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Importance of Osmolarity and Oxygen Tension for Cartilage Tissue Engineering

For cartilage repair in vivo or evaluation of new therapeutic approaches in vitro, the generation of functional cartilage tissue is of crucial importance and can only be achieved if the phenotype of the chondrocytes is preserved. Three-dimensional (3D) cell culture is broadly used for this purpose....

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Autores principales: Sieber, Stefan, Michaelis, Martin, Gühring, Hans, Lindemann, Sven, Gigout, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7133430/
https://www.ncbi.nlm.nih.gov/pubmed/32257626
http://dx.doi.org/10.1089/biores.2020.0009
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author Sieber, Stefan
Michaelis, Martin
Gühring, Hans
Lindemann, Sven
Gigout, Anne
author_facet Sieber, Stefan
Michaelis, Martin
Gühring, Hans
Lindemann, Sven
Gigout, Anne
author_sort Sieber, Stefan
collection PubMed
description For cartilage repair in vivo or evaluation of new therapeutic approaches in vitro, the generation of functional cartilage tissue is of crucial importance and can only be achieved if the phenotype of the chondrocytes is preserved. Three-dimensional (3D) cell culture is broadly used for this purpose. However, adapting culture parameters like the oxygen tension or the osmolarity to their physiological values is often omitted. Indeed, articular cartilage is an avascular tissue subjected to reduced oxygen tension and presenting and increased osmolarity compared with most other tissues. In this study, we aimed at evaluating the effect of a physiological oxygen tension (3% instead of 21%) and physiological osmolarity (430 vs. 330 mOsm in nonadjusted DMEM) and the combination of both on the cell proliferation, matrix production, and the phenotype of porcine chondrocytes in a scaffold-free 3D culture system. We observed that a physiological osmolarity had no effect on cell proliferation and matrix production but positively influences the chondrocyte phenotype. A physiological oxygen level prevented cell proliferation but resulted in an increased matrix content/million cells and had a positive influence on the chondrocyte phenotype as well. The strongest benefit was reached with the combination of both physiological osmolarity and oxygen levels; with these conditions, type I collagen expression became undetectable. In addition, at 3% O(2) the chondrocytes-matrix constructs were found to more closely resemble native cartilage regarding the matrix-to-cell ratio. In conclusion, this study clearly demonstrates the benefit of using physiological oxygen tension and osmolarity in cartilage tissue engineering with the combination of both showing the strongest benefit on the chondrocyte phenotype.
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spelling pubmed-71334302020-04-06 Importance of Osmolarity and Oxygen Tension for Cartilage Tissue Engineering Sieber, Stefan Michaelis, Martin Gühring, Hans Lindemann, Sven Gigout, Anne Biores Open Access Original Research Article For cartilage repair in vivo or evaluation of new therapeutic approaches in vitro, the generation of functional cartilage tissue is of crucial importance and can only be achieved if the phenotype of the chondrocytes is preserved. Three-dimensional (3D) cell culture is broadly used for this purpose. However, adapting culture parameters like the oxygen tension or the osmolarity to their physiological values is often omitted. Indeed, articular cartilage is an avascular tissue subjected to reduced oxygen tension and presenting and increased osmolarity compared with most other tissues. In this study, we aimed at evaluating the effect of a physiological oxygen tension (3% instead of 21%) and physiological osmolarity (430 vs. 330 mOsm in nonadjusted DMEM) and the combination of both on the cell proliferation, matrix production, and the phenotype of porcine chondrocytes in a scaffold-free 3D culture system. We observed that a physiological osmolarity had no effect on cell proliferation and matrix production but positively influences the chondrocyte phenotype. A physiological oxygen level prevented cell proliferation but resulted in an increased matrix content/million cells and had a positive influence on the chondrocyte phenotype as well. The strongest benefit was reached with the combination of both physiological osmolarity and oxygen levels; with these conditions, type I collagen expression became undetectable. In addition, at 3% O(2) the chondrocytes-matrix constructs were found to more closely resemble native cartilage regarding the matrix-to-cell ratio. In conclusion, this study clearly demonstrates the benefit of using physiological oxygen tension and osmolarity in cartilage tissue engineering with the combination of both showing the strongest benefit on the chondrocyte phenotype. Mary Ann Liebert, Inc., publishers 2020-03-31 /pmc/articles/PMC7133430/ /pubmed/32257626 http://dx.doi.org/10.1089/biores.2020.0009 Text en © Stefan Sieber et al. 2020; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Sieber, Stefan
Michaelis, Martin
Gühring, Hans
Lindemann, Sven
Gigout, Anne
Importance of Osmolarity and Oxygen Tension for Cartilage Tissue Engineering
title Importance of Osmolarity and Oxygen Tension for Cartilage Tissue Engineering
title_full Importance of Osmolarity and Oxygen Tension for Cartilage Tissue Engineering
title_fullStr Importance of Osmolarity and Oxygen Tension for Cartilage Tissue Engineering
title_full_unstemmed Importance of Osmolarity and Oxygen Tension for Cartilage Tissue Engineering
title_short Importance of Osmolarity and Oxygen Tension for Cartilage Tissue Engineering
title_sort importance of osmolarity and oxygen tension for cartilage tissue engineering
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7133430/
https://www.ncbi.nlm.nih.gov/pubmed/32257626
http://dx.doi.org/10.1089/biores.2020.0009
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