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Bioreactor-Induced Chondrocyte Maturation Is Dependent on Cell Passage and Onset of Loading

OBJECTIVE: To explore the effect of shifting in vitro culture conditions regarding cellular passage and onset of loading within matrix-associated bovine articular chondrocytes cultured under free-swelling and/or dynamical loading conditions on general chondrocyte maturation. METHODS: Primary or pass...

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Autores principales: Wang, Ning, Grad, Sibylle, Stoddart, Martin J., Niemeyer, Philipp, Südkamp, Norbert P., Pestka, Jan, Alini, Mauro, Chen, Jiying, Salzmann, Gian M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297099/
https://www.ncbi.nlm.nih.gov/pubmed/26069659
http://dx.doi.org/10.1177/1947603512471345
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author Wang, Ning
Grad, Sibylle
Stoddart, Martin J.
Niemeyer, Philipp
Südkamp, Norbert P.
Pestka, Jan
Alini, Mauro
Chen, Jiying
Salzmann, Gian M.
author_facet Wang, Ning
Grad, Sibylle
Stoddart, Martin J.
Niemeyer, Philipp
Südkamp, Norbert P.
Pestka, Jan
Alini, Mauro
Chen, Jiying
Salzmann, Gian M.
author_sort Wang, Ning
collection PubMed
description OBJECTIVE: To explore the effect of shifting in vitro culture conditions regarding cellular passage and onset of loading within matrix-associated bovine articular chondrocytes cultured under free-swelling and/or dynamical loading conditions on general chondrocyte maturation. METHODS: Primary or passage 3 bovine chondrocytes were seeded in fibrin-polyurethane scaffolds. Constructs were cultured either free-swelling for 2 or 4 weeks, under direct mechanical loading for 2 or 4 weeks, or free swelling for 2 weeks followed by 2 weeks of loading. Samples were collected for glycosaminoglycan (GAG) quantification, mRNA expression of chondrogenic genes, immunohistochemistry, and histology. RESULTS: Mechanical loading generally stimulated GAG synthesis, up-regulated chondrogenic genes, and improved the accumulation of matrix in cell-laden constructs when compared with free-swelling controls. Primary chondrocytes underwent more effective cartilage maturation when compared with passaged chondrocytes. Constructs of primary chondrocytes that were initially free-swelling followed by 2 weeks of mechanical load (delayed) had overall highest GAG with strongest responsiveness to load regarding matrix synthesis. Constructs that experienced the delayed loading regime also demonstrated most favorable chondrogenic gene expression profiles in both primary and third passage cells. Furthermore, most intense matrix staining and immunostaining of collagen type II and aggrecan were visualized in these constructs. CONCLUSIONS: Primary chondrocytes were more effective than passage 3 chondrocytes when chondrogenesis was concerned. The most efficient chondrogenesis resulted from primary articular chondrocytes, which were initially free-swelling followed by a standardized loading protocol.
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spelling pubmed-42970992015-06-11 Bioreactor-Induced Chondrocyte Maturation Is Dependent on Cell Passage and Onset of Loading Wang, Ning Grad, Sibylle Stoddart, Martin J. Niemeyer, Philipp Südkamp, Norbert P. Pestka, Jan Alini, Mauro Chen, Jiying Salzmann, Gian M. Cartilage Article OBJECTIVE: To explore the effect of shifting in vitro culture conditions regarding cellular passage and onset of loading within matrix-associated bovine articular chondrocytes cultured under free-swelling and/or dynamical loading conditions on general chondrocyte maturation. METHODS: Primary or passage 3 bovine chondrocytes were seeded in fibrin-polyurethane scaffolds. Constructs were cultured either free-swelling for 2 or 4 weeks, under direct mechanical loading for 2 or 4 weeks, or free swelling for 2 weeks followed by 2 weeks of loading. Samples were collected for glycosaminoglycan (GAG) quantification, mRNA expression of chondrogenic genes, immunohistochemistry, and histology. RESULTS: Mechanical loading generally stimulated GAG synthesis, up-regulated chondrogenic genes, and improved the accumulation of matrix in cell-laden constructs when compared with free-swelling controls. Primary chondrocytes underwent more effective cartilage maturation when compared with passaged chondrocytes. Constructs of primary chondrocytes that were initially free-swelling followed by 2 weeks of mechanical load (delayed) had overall highest GAG with strongest responsiveness to load regarding matrix synthesis. Constructs that experienced the delayed loading regime also demonstrated most favorable chondrogenic gene expression profiles in both primary and third passage cells. Furthermore, most intense matrix staining and immunostaining of collagen type II and aggrecan were visualized in these constructs. CONCLUSIONS: Primary chondrocytes were more effective than passage 3 chondrocytes when chondrogenesis was concerned. The most efficient chondrogenesis resulted from primary articular chondrocytes, which were initially free-swelling followed by a standardized loading protocol. SAGE Publications 2013-04 /pmc/articles/PMC4297099/ /pubmed/26069659 http://dx.doi.org/10.1177/1947603512471345 Text en © The Author(s) 2012
spellingShingle Article
Wang, Ning
Grad, Sibylle
Stoddart, Martin J.
Niemeyer, Philipp
Südkamp, Norbert P.
Pestka, Jan
Alini, Mauro
Chen, Jiying
Salzmann, Gian M.
Bioreactor-Induced Chondrocyte Maturation Is Dependent on Cell Passage and Onset of Loading
title Bioreactor-Induced Chondrocyte Maturation Is Dependent on Cell Passage and Onset of Loading
title_full Bioreactor-Induced Chondrocyte Maturation Is Dependent on Cell Passage and Onset of Loading
title_fullStr Bioreactor-Induced Chondrocyte Maturation Is Dependent on Cell Passage and Onset of Loading
title_full_unstemmed Bioreactor-Induced Chondrocyte Maturation Is Dependent on Cell Passage and Onset of Loading
title_short Bioreactor-Induced Chondrocyte Maturation Is Dependent on Cell Passage and Onset of Loading
title_sort bioreactor-induced chondrocyte maturation is dependent on cell passage and onset of loading
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297099/
https://www.ncbi.nlm.nih.gov/pubmed/26069659
http://dx.doi.org/10.1177/1947603512471345
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