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M1-like macrophage contributes to chondrogenesis in vitro
Cartilage tissues have poor self-repairing abilities. Regenerative medicine can be applied to recover cartilage tissue damage in the oral and maxillofacial regions. However, hitherto it has not been possible to predict the maturity of the tissue construction after transplantation or to prepare matur...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556372/ https://www.ncbi.nlm.nih.gov/pubmed/34716346 http://dx.doi.org/10.1038/s41598-021-00232-7 |
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author | Miyamoto, Yoshiyuki Kubota, Keigo Asawa, Yukiyo Hoshi, Kazuto Hikita, Atsuhiko |
author_facet | Miyamoto, Yoshiyuki Kubota, Keigo Asawa, Yukiyo Hoshi, Kazuto Hikita, Atsuhiko |
author_sort | Miyamoto, Yoshiyuki |
collection | PubMed |
description | Cartilage tissues have poor self-repairing abilities. Regenerative medicine can be applied to recover cartilage tissue damage in the oral and maxillofacial regions. However, hitherto it has not been possible to predict the maturity of the tissue construction after transplantation or to prepare mature cartilage tissues before transplantation that can meet clinical needs. Macrophages play an important role in cartilage tissue regeneration, although the exact mechanisms remain unknown. In this study, we established and verified an in vitro experimental system for the direct co-culture of cell pellets prepared from mouse auricular chondrocytes and macrophages polarized into four phenotypes (M1-like, M1, M2-like, and M2). We demonstrate that cartilage pellets co-cultured with M1-like promoted collagen type 2 and aggrecan production and induced the most significant increase in chondrogenesis. Furthermore, M1-like shifted to M2 on day 7 of co-culture, suggesting that the cartilage pellet supplied factors that changed the polarization of M1-like. Our findings suggest that cartilage regenerative medicine will be most effective if the maturation of cartilage tissues is induced in vitro by co-culture with M1-like before transplantation. |
format | Online Article Text |
id | pubmed-8556372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85563722021-11-03 M1-like macrophage contributes to chondrogenesis in vitro Miyamoto, Yoshiyuki Kubota, Keigo Asawa, Yukiyo Hoshi, Kazuto Hikita, Atsuhiko Sci Rep Article Cartilage tissues have poor self-repairing abilities. Regenerative medicine can be applied to recover cartilage tissue damage in the oral and maxillofacial regions. However, hitherto it has not been possible to predict the maturity of the tissue construction after transplantation or to prepare mature cartilage tissues before transplantation that can meet clinical needs. Macrophages play an important role in cartilage tissue regeneration, although the exact mechanisms remain unknown. In this study, we established and verified an in vitro experimental system for the direct co-culture of cell pellets prepared from mouse auricular chondrocytes and macrophages polarized into four phenotypes (M1-like, M1, M2-like, and M2). We demonstrate that cartilage pellets co-cultured with M1-like promoted collagen type 2 and aggrecan production and induced the most significant increase in chondrogenesis. Furthermore, M1-like shifted to M2 on day 7 of co-culture, suggesting that the cartilage pellet supplied factors that changed the polarization of M1-like. Our findings suggest that cartilage regenerative medicine will be most effective if the maturation of cartilage tissues is induced in vitro by co-culture with M1-like before transplantation. Nature Publishing Group UK 2021-10-29 /pmc/articles/PMC8556372/ /pubmed/34716346 http://dx.doi.org/10.1038/s41598-021-00232-7 Text en © The Author(s) 2021, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Miyamoto, Yoshiyuki Kubota, Keigo Asawa, Yukiyo Hoshi, Kazuto Hikita, Atsuhiko M1-like macrophage contributes to chondrogenesis in vitro |
title | M1-like macrophage contributes to chondrogenesis in vitro |
title_full | M1-like macrophage contributes to chondrogenesis in vitro |
title_fullStr | M1-like macrophage contributes to chondrogenesis in vitro |
title_full_unstemmed | M1-like macrophage contributes to chondrogenesis in vitro |
title_short | M1-like macrophage contributes to chondrogenesis in vitro |
title_sort | m1-like macrophage contributes to chondrogenesis in vitro |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556372/ https://www.ncbi.nlm.nih.gov/pubmed/34716346 http://dx.doi.org/10.1038/s41598-021-00232-7 |
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