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Meniscal fibrocartilage regeneration inspired by meniscal maturational and regenerative process
Meniscus is a complex and crucial fibrocartilaginous tissue within the knee joint. Meniscal regeneration remains to be a scientific and translational challenge. We clarified that mesenchymal stem cells (MSCs) participated in meniscal maturation and regeneration using MSC-tracing transgenic mice mode...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10631723/ https://www.ncbi.nlm.nih.gov/pubmed/37939174 http://dx.doi.org/10.1126/sciadv.adg8138 |
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author | Yan, Wenqiang Maimaitimin, Maihemuti Wu, Yue Fan, Yifei Ren, Shuang Zhao, Fengyuan Cao, Chenxi Hu, Xiaoqing Cheng, Jin Ao, Yingfang |
author_facet | Yan, Wenqiang Maimaitimin, Maihemuti Wu, Yue Fan, Yifei Ren, Shuang Zhao, Fengyuan Cao, Chenxi Hu, Xiaoqing Cheng, Jin Ao, Yingfang |
author_sort | Yan, Wenqiang |
collection | PubMed |
description | Meniscus is a complex and crucial fibrocartilaginous tissue within the knee joint. Meniscal regeneration remains to be a scientific and translational challenge. We clarified that mesenchymal stem cells (MSCs) participated in meniscal maturation and regeneration using MSC-tracing transgenic mice model. Here, inspired by meniscal natural maturational and regenerative process, we developed an effective and translational strategy to facilitate meniscal regeneration by three-dimensionally printing biomimetic meniscal scaffold combining autologous synovium transplant, which contained abundant intrinsic MSCs. We verified that this facilitated anisotropic meniscus–like tissue regeneration and protected cartilage from degeneration in large animal model. Mechanistically, the biomechanics and matrix stiffness up-regulated Piezo1 expression, facilitating concerted activation of calcineurin and NFATc1, further activated YAP-pSmad2/3-SOX9 axis, and consequently facilitated fibrochondrogenesis of MSCs during meniscal regeneration. In addition, Piezo1 induced by biomechanics and matrix stiffness up-regulated collagen cross-link enzyme expression, which catalyzed collagen cross-link and thereby enhanced mechanical properties of regenerated tissue. |
format | Online Article Text |
id | pubmed-10631723 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-106317232023-11-10 Meniscal fibrocartilage regeneration inspired by meniscal maturational and regenerative process Yan, Wenqiang Maimaitimin, Maihemuti Wu, Yue Fan, Yifei Ren, Shuang Zhao, Fengyuan Cao, Chenxi Hu, Xiaoqing Cheng, Jin Ao, Yingfang Sci Adv Biomedicine and Life Sciences Meniscus is a complex and crucial fibrocartilaginous tissue within the knee joint. Meniscal regeneration remains to be a scientific and translational challenge. We clarified that mesenchymal stem cells (MSCs) participated in meniscal maturation and regeneration using MSC-tracing transgenic mice model. Here, inspired by meniscal natural maturational and regenerative process, we developed an effective and translational strategy to facilitate meniscal regeneration by three-dimensionally printing biomimetic meniscal scaffold combining autologous synovium transplant, which contained abundant intrinsic MSCs. We verified that this facilitated anisotropic meniscus–like tissue regeneration and protected cartilage from degeneration in large animal model. Mechanistically, the biomechanics and matrix stiffness up-regulated Piezo1 expression, facilitating concerted activation of calcineurin and NFATc1, further activated YAP-pSmad2/3-SOX9 axis, and consequently facilitated fibrochondrogenesis of MSCs during meniscal regeneration. In addition, Piezo1 induced by biomechanics and matrix stiffness up-regulated collagen cross-link enzyme expression, which catalyzed collagen cross-link and thereby enhanced mechanical properties of regenerated tissue. American Association for the Advancement of Science 2023-11-08 /pmc/articles/PMC10631723/ /pubmed/37939174 http://dx.doi.org/10.1126/sciadv.adg8138 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Yan, Wenqiang Maimaitimin, Maihemuti Wu, Yue Fan, Yifei Ren, Shuang Zhao, Fengyuan Cao, Chenxi Hu, Xiaoqing Cheng, Jin Ao, Yingfang Meniscal fibrocartilage regeneration inspired by meniscal maturational and regenerative process |
title | Meniscal fibrocartilage regeneration inspired by meniscal maturational and regenerative process |
title_full | Meniscal fibrocartilage regeneration inspired by meniscal maturational and regenerative process |
title_fullStr | Meniscal fibrocartilage regeneration inspired by meniscal maturational and regenerative process |
title_full_unstemmed | Meniscal fibrocartilage regeneration inspired by meniscal maturational and regenerative process |
title_short | Meniscal fibrocartilage regeneration inspired by meniscal maturational and regenerative process |
title_sort | meniscal fibrocartilage regeneration inspired by meniscal maturational and regenerative process |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10631723/ https://www.ncbi.nlm.nih.gov/pubmed/37939174 http://dx.doi.org/10.1126/sciadv.adg8138 |
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