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Induced regeneration of articular cartilage – identification of a dormant regeneration program for a non-regenerative tissue

A mouse organoid culture model was developed to regenerate articular cartilage by sequential treatment with BMP2 and BMP9 (or GDF2) that parallels induced joint regeneration at digit amputation wounds in vivo. BMP9-induced chondrogenesis was used to identify clonal cell lines for articular chondrocy...

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Autores principales: Lin, Yu-Lieh, Yu, Ling, Yan, Mingquan, Zimmel, Katherine, Qureshi, Osama, Imholt, Felisha, Li, Tao, Ivanov, Ivan, Brunauer, Regina, Dawson, Lindsay, Muneoka, Ken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651102/
https://www.ncbi.nlm.nih.gov/pubmed/37882667
http://dx.doi.org/10.1242/dev.201894
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author Lin, Yu-Lieh
Yu, Ling
Yan, Mingquan
Zimmel, Katherine
Qureshi, Osama
Imholt, Felisha
Li, Tao
Ivanov, Ivan
Brunauer, Regina
Dawson, Lindsay
Muneoka, Ken
author_facet Lin, Yu-Lieh
Yu, Ling
Yan, Mingquan
Zimmel, Katherine
Qureshi, Osama
Imholt, Felisha
Li, Tao
Ivanov, Ivan
Brunauer, Regina
Dawson, Lindsay
Muneoka, Ken
author_sort Lin, Yu-Lieh
collection PubMed
description A mouse organoid culture model was developed to regenerate articular cartilage by sequential treatment with BMP2 and BMP9 (or GDF2) that parallels induced joint regeneration at digit amputation wounds in vivo. BMP9-induced chondrogenesis was used to identify clonal cell lines for articular chondrocyte and hypertrophic chondrocyte progenitor cells from digit fibroblasts. A protocol that includes cell aggregation enhanced by BMP2 followed by BMP9-induced chondrogenesis resulted in the differentiation of organized layers of articular chondrocytes, similar to the organization of middle and deep zones of articular cartilage in situ, and retained a differentiated phenotype following transplantation. In addition, the differentiation of a non-chondrogenic connective tissue layer containing articular chondrocyte progenitor cells demonstrated that progenitor cell sequestration is coupled with articular cartilage differentiation at a clonal level. The studies identify a dormant endogenous regenerative program for a non-regenerative tissue in which fibroblast-derived progenitor cells can be induced to initiate morphogenetic and differentiative programs that include progenitor cell sequestration. The identification of dormant regenerative programs in non-regenerative tissues such as articular cartilage represents a novel strategy that integrates regeneration biology with regenerative medicine.
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spelling pubmed-106511022023-11-08 Induced regeneration of articular cartilage – identification of a dormant regeneration program for a non-regenerative tissue Lin, Yu-Lieh Yu, Ling Yan, Mingquan Zimmel, Katherine Qureshi, Osama Imholt, Felisha Li, Tao Ivanov, Ivan Brunauer, Regina Dawson, Lindsay Muneoka, Ken Development Stem Cells and Regeneration A mouse organoid culture model was developed to regenerate articular cartilage by sequential treatment with BMP2 and BMP9 (or GDF2) that parallels induced joint regeneration at digit amputation wounds in vivo. BMP9-induced chondrogenesis was used to identify clonal cell lines for articular chondrocyte and hypertrophic chondrocyte progenitor cells from digit fibroblasts. A protocol that includes cell aggregation enhanced by BMP2 followed by BMP9-induced chondrogenesis resulted in the differentiation of organized layers of articular chondrocytes, similar to the organization of middle and deep zones of articular cartilage in situ, and retained a differentiated phenotype following transplantation. In addition, the differentiation of a non-chondrogenic connective tissue layer containing articular chondrocyte progenitor cells demonstrated that progenitor cell sequestration is coupled with articular cartilage differentiation at a clonal level. The studies identify a dormant endogenous regenerative program for a non-regenerative tissue in which fibroblast-derived progenitor cells can be induced to initiate morphogenetic and differentiative programs that include progenitor cell sequestration. The identification of dormant regenerative programs in non-regenerative tissues such as articular cartilage represents a novel strategy that integrates regeneration biology with regenerative medicine. The Company of Biologists Ltd 2023-11-08 /pmc/articles/PMC10651102/ /pubmed/37882667 http://dx.doi.org/10.1242/dev.201894 Text en © 2023. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Stem Cells and Regeneration
Lin, Yu-Lieh
Yu, Ling
Yan, Mingquan
Zimmel, Katherine
Qureshi, Osama
Imholt, Felisha
Li, Tao
Ivanov, Ivan
Brunauer, Regina
Dawson, Lindsay
Muneoka, Ken
Induced regeneration of articular cartilage – identification of a dormant regeneration program for a non-regenerative tissue
title Induced regeneration of articular cartilage – identification of a dormant regeneration program for a non-regenerative tissue
title_full Induced regeneration of articular cartilage – identification of a dormant regeneration program for a non-regenerative tissue
title_fullStr Induced regeneration of articular cartilage – identification of a dormant regeneration program for a non-regenerative tissue
title_full_unstemmed Induced regeneration of articular cartilage – identification of a dormant regeneration program for a non-regenerative tissue
title_short Induced regeneration of articular cartilage – identification of a dormant regeneration program for a non-regenerative tissue
title_sort induced regeneration of articular cartilage – identification of a dormant regeneration program for a non-regenerative tissue
topic Stem Cells and Regeneration
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651102/
https://www.ncbi.nlm.nih.gov/pubmed/37882667
http://dx.doi.org/10.1242/dev.201894
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