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Comparison between articular chondrocytes and mesenchymal stromal cells for the production of articular cartilage implants
Focal lesions of articular cartilage give rise to pain and reduced joint function and may, if left untreated, lead to osteoarthritis. Implantation of in vitro generated, scaffold-free autologous cartilage discs may represent the best treatment option. Here we compare articular chondrocytes (ACs) and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9989206/ https://www.ncbi.nlm.nih.gov/pubmed/36896010 http://dx.doi.org/10.3389/fbioe.2023.1116513 |
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author | Frerker, Nadine Karlsen, Tommy A. Stensland, Maria Nyman, Tuula A. Rayner, Simon Brinchmann, Jan E. |
author_facet | Frerker, Nadine Karlsen, Tommy A. Stensland, Maria Nyman, Tuula A. Rayner, Simon Brinchmann, Jan E. |
author_sort | Frerker, Nadine |
collection | PubMed |
description | Focal lesions of articular cartilage give rise to pain and reduced joint function and may, if left untreated, lead to osteoarthritis. Implantation of in vitro generated, scaffold-free autologous cartilage discs may represent the best treatment option. Here we compare articular chondrocytes (ACs) and bone marrow-derived mesenchymal stromal cells (MSCs) for their ability to make scaffold-free cartilage discs. Articular chondrocytes produced more extracellular matrix per seeded cell than mesenchymal stromal cells. Quantitative proteomics analysis showed that articular chondrocyte discs contained more articular cartilage proteins, while mesenchymal stromal cell discs had more proteins associated with cartilage hypertrophy and bone formation. Sequencing analysis revealed more microRNAs associated with normal cartilage in articular chondrocyte discs, and large-scale target predictions, performed for the first time for in vitro chondrogenesis, suggested that differential expression of microRNAs in the two disc types were important mechanisms behind differential synthesis of proteins. We conclude that articular chondrocytes should be preferred over mesenchymal stromal cells for tissue engineering of articular cartilage. |
format | Online Article Text |
id | pubmed-9989206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99892062023-03-08 Comparison between articular chondrocytes and mesenchymal stromal cells for the production of articular cartilage implants Frerker, Nadine Karlsen, Tommy A. Stensland, Maria Nyman, Tuula A. Rayner, Simon Brinchmann, Jan E. Front Bioeng Biotechnol Bioengineering and Biotechnology Focal lesions of articular cartilage give rise to pain and reduced joint function and may, if left untreated, lead to osteoarthritis. Implantation of in vitro generated, scaffold-free autologous cartilage discs may represent the best treatment option. Here we compare articular chondrocytes (ACs) and bone marrow-derived mesenchymal stromal cells (MSCs) for their ability to make scaffold-free cartilage discs. Articular chondrocytes produced more extracellular matrix per seeded cell than mesenchymal stromal cells. Quantitative proteomics analysis showed that articular chondrocyte discs contained more articular cartilage proteins, while mesenchymal stromal cell discs had more proteins associated with cartilage hypertrophy and bone formation. Sequencing analysis revealed more microRNAs associated with normal cartilage in articular chondrocyte discs, and large-scale target predictions, performed for the first time for in vitro chondrogenesis, suggested that differential expression of microRNAs in the two disc types were important mechanisms behind differential synthesis of proteins. We conclude that articular chondrocytes should be preferred over mesenchymal stromal cells for tissue engineering of articular cartilage. Frontiers Media S.A. 2023-02-21 /pmc/articles/PMC9989206/ /pubmed/36896010 http://dx.doi.org/10.3389/fbioe.2023.1116513 Text en Copyright © 2023 Frerker, Karlsen, Stensland, Nyman, Rayner and Brinchmann. 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 Frerker, Nadine Karlsen, Tommy A. Stensland, Maria Nyman, Tuula A. Rayner, Simon Brinchmann, Jan E. Comparison between articular chondrocytes and mesenchymal stromal cells for the production of articular cartilage implants |
title | Comparison between articular chondrocytes and mesenchymal stromal cells for the production of articular cartilage implants |
title_full | Comparison between articular chondrocytes and mesenchymal stromal cells for the production of articular cartilage implants |
title_fullStr | Comparison between articular chondrocytes and mesenchymal stromal cells for the production of articular cartilage implants |
title_full_unstemmed | Comparison between articular chondrocytes and mesenchymal stromal cells for the production of articular cartilage implants |
title_short | Comparison between articular chondrocytes and mesenchymal stromal cells for the production of articular cartilage implants |
title_sort | comparison between articular chondrocytes and mesenchymal stromal cells for the production of articular cartilage implants |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9989206/ https://www.ncbi.nlm.nih.gov/pubmed/36896010 http://dx.doi.org/10.3389/fbioe.2023.1116513 |
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