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Primary cilia support cartilage regeneration after injury
In growing children, growth plate cartilage has limited self-repair ability upon fracture injury always leading to limb growth arrest. Interestingly, one type of fracture injuries within the growth plate achieve amazing self-healing, however, the mechanism is unclear. Using this type of fracture mou...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238430/ https://www.ncbi.nlm.nih.gov/pubmed/37268650 http://dx.doi.org/10.1038/s41368-023-00223-6 |
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author | Tao, Dike Zhang, Lei Ding, Yunpeng Tang, Na Xu, Xiaoqiao Li, Gongchen Niu, Pingping Yue, Rui Wang, Xiaogang Shen, Yidong Sun, Yao |
author_facet | Tao, Dike Zhang, Lei Ding, Yunpeng Tang, Na Xu, Xiaoqiao Li, Gongchen Niu, Pingping Yue, Rui Wang, Xiaogang Shen, Yidong Sun, Yao |
author_sort | Tao, Dike |
collection | PubMed |
description | In growing children, growth plate cartilage has limited self-repair ability upon fracture injury always leading to limb growth arrest. Interestingly, one type of fracture injuries within the growth plate achieve amazing self-healing, however, the mechanism is unclear. Using this type of fracture mouse model, we discovered the activation of Hedgehog (Hh) signaling in the injured growth plate, which could activate chondrocytes in growth plate and promote cartilage repair. Primary cilia are the central transduction mediator of Hh signaling. Notably, ciliary Hh-Smo-Gli signaling pathways were enriched in the growth plate during development. Moreover, chondrocytes in resting and proliferating zone were dynamically ciliated during growth plate repair. Furthermore, conditional deletion of the ciliary core gene Ift140 in cartilage disrupted cilia-mediated Hh signaling in growth plate. More importantly, activating ciliary Hh signaling by Smoothened agonist (SAG) significantly accelerated growth plate repair after injury. In sum, primary cilia mediate Hh signaling induced the activation of stem/progenitor chondrocytes and growth plate repair after fracture injury. |
format | Online Article Text |
id | pubmed-10238430 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102384302023-06-04 Primary cilia support cartilage regeneration after injury Tao, Dike Zhang, Lei Ding, Yunpeng Tang, Na Xu, Xiaoqiao Li, Gongchen Niu, Pingping Yue, Rui Wang, Xiaogang Shen, Yidong Sun, Yao Int J Oral Sci Article In growing children, growth plate cartilage has limited self-repair ability upon fracture injury always leading to limb growth arrest. Interestingly, one type of fracture injuries within the growth plate achieve amazing self-healing, however, the mechanism is unclear. Using this type of fracture mouse model, we discovered the activation of Hedgehog (Hh) signaling in the injured growth plate, which could activate chondrocytes in growth plate and promote cartilage repair. Primary cilia are the central transduction mediator of Hh signaling. Notably, ciliary Hh-Smo-Gli signaling pathways were enriched in the growth plate during development. Moreover, chondrocytes in resting and proliferating zone were dynamically ciliated during growth plate repair. Furthermore, conditional deletion of the ciliary core gene Ift140 in cartilage disrupted cilia-mediated Hh signaling in growth plate. More importantly, activating ciliary Hh signaling by Smoothened agonist (SAG) significantly accelerated growth plate repair after injury. In sum, primary cilia mediate Hh signaling induced the activation of stem/progenitor chondrocytes and growth plate repair after fracture injury. Nature Publishing Group UK 2023-06-02 /pmc/articles/PMC10238430/ /pubmed/37268650 http://dx.doi.org/10.1038/s41368-023-00223-6 Text en © The Author(s) 2023 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Tao, Dike Zhang, Lei Ding, Yunpeng Tang, Na Xu, Xiaoqiao Li, Gongchen Niu, Pingping Yue, Rui Wang, Xiaogang Shen, Yidong Sun, Yao Primary cilia support cartilage regeneration after injury |
title | Primary cilia support cartilage regeneration after injury |
title_full | Primary cilia support cartilage regeneration after injury |
title_fullStr | Primary cilia support cartilage regeneration after injury |
title_full_unstemmed | Primary cilia support cartilage regeneration after injury |
title_short | Primary cilia support cartilage regeneration after injury |
title_sort | primary cilia support cartilage regeneration after injury |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238430/ https://www.ncbi.nlm.nih.gov/pubmed/37268650 http://dx.doi.org/10.1038/s41368-023-00223-6 |
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