Cargando…

Synoviocyte-Derived Extracellular Matrix and bFGF Speed Human Chondrocyte Proliferation While Maintaining Differentiation Potential

Improving the ability of human chondrocytes to proliferate, while maintaining their differentiation potential, has presented a great challenge in cartilage tissue engineering. In this study, human chondrocytes were cultured under four unique growth conditions at physiologic oxygen tension: tissue cu...

Descripción completa

Detalles Bibliográficos
Autores principales: Truong, Rachel D., Bernier, Megan A., Dennis, James E., Kean, Thomas J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9171110/
https://www.ncbi.nlm.nih.gov/pubmed/35685088
http://dx.doi.org/10.3389/fbioe.2022.825005
_version_ 1784721591293181952
author Truong, Rachel D.
Bernier, Megan A.
Dennis, James E.
Kean, Thomas J.
author_facet Truong, Rachel D.
Bernier, Megan A.
Dennis, James E.
Kean, Thomas J.
author_sort Truong, Rachel D.
collection PubMed
description Improving the ability of human chondrocytes to proliferate, while maintaining their differentiation potential, has presented a great challenge in cartilage tissue engineering. In this study, human chondrocytes were cultured under four unique growth conditions at physiologic oxygen tension: tissue culture plastic (TCP) only, synoviocyte matrix (SCM)–coated flasks only, SCM-coated flasks with bFGF media supplement, and TCP with bFGF media supplement. The results indicated that, compared to standard TCP, all test conditions showed significantly increased cell expansion rates and an increase in both glycosaminoglycan (GAG) and collagen content during redifferentiation culture. Specifically, the combined SCM + bFGF growth condition showed an additive effect, with an increase of approximately 36% more cells per passage (5–7 days) when compared to the SCM alone. In conclusion, the results of this study demonstrate that bFGF and SCM can be used as supplements to enhance the growth of human chondrocytes both as individual enhancers and as a combined additive.
format Online
Article
Text
id pubmed-9171110
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-91711102022-06-08 Synoviocyte-Derived Extracellular Matrix and bFGF Speed Human Chondrocyte Proliferation While Maintaining Differentiation Potential Truong, Rachel D. Bernier, Megan A. Dennis, James E. Kean, Thomas J. Front Bioeng Biotechnol Bioengineering and Biotechnology Improving the ability of human chondrocytes to proliferate, while maintaining their differentiation potential, has presented a great challenge in cartilage tissue engineering. In this study, human chondrocytes were cultured under four unique growth conditions at physiologic oxygen tension: tissue culture plastic (TCP) only, synoviocyte matrix (SCM)–coated flasks only, SCM-coated flasks with bFGF media supplement, and TCP with bFGF media supplement. The results indicated that, compared to standard TCP, all test conditions showed significantly increased cell expansion rates and an increase in both glycosaminoglycan (GAG) and collagen content during redifferentiation culture. Specifically, the combined SCM + bFGF growth condition showed an additive effect, with an increase of approximately 36% more cells per passage (5–7 days) when compared to the SCM alone. In conclusion, the results of this study demonstrate that bFGF and SCM can be used as supplements to enhance the growth of human chondrocytes both as individual enhancers and as a combined additive. Frontiers Media S.A. 2022-05-24 /pmc/articles/PMC9171110/ /pubmed/35685088 http://dx.doi.org/10.3389/fbioe.2022.825005 Text en Copyright © 2022 Truong, Bernier, Dennis and Kean. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Truong, Rachel D.
Bernier, Megan A.
Dennis, James E.
Kean, Thomas J.
Synoviocyte-Derived Extracellular Matrix and bFGF Speed Human Chondrocyte Proliferation While Maintaining Differentiation Potential
title Synoviocyte-Derived Extracellular Matrix and bFGF Speed Human Chondrocyte Proliferation While Maintaining Differentiation Potential
title_full Synoviocyte-Derived Extracellular Matrix and bFGF Speed Human Chondrocyte Proliferation While Maintaining Differentiation Potential
title_fullStr Synoviocyte-Derived Extracellular Matrix and bFGF Speed Human Chondrocyte Proliferation While Maintaining Differentiation Potential
title_full_unstemmed Synoviocyte-Derived Extracellular Matrix and bFGF Speed Human Chondrocyte Proliferation While Maintaining Differentiation Potential
title_short Synoviocyte-Derived Extracellular Matrix and bFGF Speed Human Chondrocyte Proliferation While Maintaining Differentiation Potential
title_sort synoviocyte-derived extracellular matrix and bfgf speed human chondrocyte proliferation while maintaining differentiation potential
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9171110/
https://www.ncbi.nlm.nih.gov/pubmed/35685088
http://dx.doi.org/10.3389/fbioe.2022.825005
work_keys_str_mv AT truongracheld synoviocytederivedextracellularmatrixandbfgfspeedhumanchondrocyteproliferationwhilemaintainingdifferentiationpotential
AT berniermegana synoviocytederivedextracellularmatrixandbfgfspeedhumanchondrocyteproliferationwhilemaintainingdifferentiationpotential
AT dennisjamese synoviocytederivedextracellularmatrixandbfgfspeedhumanchondrocyteproliferationwhilemaintainingdifferentiationpotential
AT keanthomasj synoviocytederivedextracellularmatrixandbfgfspeedhumanchondrocyteproliferationwhilemaintainingdifferentiationpotential