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CCL21/CCR7 axis regulating juvenile cartilage repair can enhance cartilage healing in adults
Juvenile tissue healing is capable of extensive scarless healing that is distinct from the scar-forming process of the adult healing response. Although many growth factors can be found in the juvenile healing process, the molecular mechanisms of juvenile tissue healing are poorly understood. Here we...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6435673/ https://www.ncbi.nlm.nih.gov/pubmed/30914733 http://dx.doi.org/10.1038/s41598-019-41621-3 |
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author | Joutoku, Zenta Onodera, Tomohiro Matsuoka, Masatake Homan, Kentaro Momma, Daisuke Baba, Rikiya Hontani, Kazutoshi Hamasaki, Masanari Matsubara, Shinji Hishimura, Ryosuke Iwasaki, Norimasa |
author_facet | Joutoku, Zenta Onodera, Tomohiro Matsuoka, Masatake Homan, Kentaro Momma, Daisuke Baba, Rikiya Hontani, Kazutoshi Hamasaki, Masanari Matsubara, Shinji Hishimura, Ryosuke Iwasaki, Norimasa |
author_sort | Joutoku, Zenta |
collection | PubMed |
description | Juvenile tissue healing is capable of extensive scarless healing that is distinct from the scar-forming process of the adult healing response. Although many growth factors can be found in the juvenile healing process, the molecular mechanisms of juvenile tissue healing are poorly understood. Here we show that juvenile mice deficient in the chemokine receptor CCR7 exhibit diminished large-scale healing potential, whereas CCR7-depleted adult mice undergo normal scar-forming healing similar to wild type mice. In addition, the CCR7 ligand CCL21 was transiently expressed around damaged cartilage in juvenile mice, whereas it is rarely expressed in adults. Notably, exogenous CCL21 administration to adults decreased scar-forming healing and enhanced hyaline-cartilage repair in rabbit osteochondral defects. Our data indicate that the CCL21/CCR7 axis may play a role in the molecular control mechanism of juvenile cartilage repair, raising the possibility that agents modulating the production of CCL21 in vivo can improve the quality of cartilage repair in adults. Such a strategy may prevent post-traumatic arthritis by mimicking the self-repair in juvenile individuals. |
format | Online Article Text |
id | pubmed-6435673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64356732019-04-02 CCL21/CCR7 axis regulating juvenile cartilage repair can enhance cartilage healing in adults Joutoku, Zenta Onodera, Tomohiro Matsuoka, Masatake Homan, Kentaro Momma, Daisuke Baba, Rikiya Hontani, Kazutoshi Hamasaki, Masanari Matsubara, Shinji Hishimura, Ryosuke Iwasaki, Norimasa Sci Rep Article Juvenile tissue healing is capable of extensive scarless healing that is distinct from the scar-forming process of the adult healing response. Although many growth factors can be found in the juvenile healing process, the molecular mechanisms of juvenile tissue healing are poorly understood. Here we show that juvenile mice deficient in the chemokine receptor CCR7 exhibit diminished large-scale healing potential, whereas CCR7-depleted adult mice undergo normal scar-forming healing similar to wild type mice. In addition, the CCR7 ligand CCL21 was transiently expressed around damaged cartilage in juvenile mice, whereas it is rarely expressed in adults. Notably, exogenous CCL21 administration to adults decreased scar-forming healing and enhanced hyaline-cartilage repair in rabbit osteochondral defects. Our data indicate that the CCL21/CCR7 axis may play a role in the molecular control mechanism of juvenile cartilage repair, raising the possibility that agents modulating the production of CCL21 in vivo can improve the quality of cartilage repair in adults. Such a strategy may prevent post-traumatic arthritis by mimicking the self-repair in juvenile individuals. Nature Publishing Group UK 2019-03-26 /pmc/articles/PMC6435673/ /pubmed/30914733 http://dx.doi.org/10.1038/s41598-019-41621-3 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Joutoku, Zenta Onodera, Tomohiro Matsuoka, Masatake Homan, Kentaro Momma, Daisuke Baba, Rikiya Hontani, Kazutoshi Hamasaki, Masanari Matsubara, Shinji Hishimura, Ryosuke Iwasaki, Norimasa CCL21/CCR7 axis regulating juvenile cartilage repair can enhance cartilage healing in adults |
title | CCL21/CCR7 axis regulating juvenile cartilage repair can enhance cartilage healing in adults |
title_full | CCL21/CCR7 axis regulating juvenile cartilage repair can enhance cartilage healing in adults |
title_fullStr | CCL21/CCR7 axis regulating juvenile cartilage repair can enhance cartilage healing in adults |
title_full_unstemmed | CCL21/CCR7 axis regulating juvenile cartilage repair can enhance cartilage healing in adults |
title_short | CCL21/CCR7 axis regulating juvenile cartilage repair can enhance cartilage healing in adults |
title_sort | ccl21/ccr7 axis regulating juvenile cartilage repair can enhance cartilage healing in adults |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6435673/ https://www.ncbi.nlm.nih.gov/pubmed/30914733 http://dx.doi.org/10.1038/s41598-019-41621-3 |
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