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Sox9 Potentiates BMP2-Induced Chondrogenic Differentiation and Inhibits BMP2-Induced Osteogenic Differentiation

Bone morphogenetic protein 2 (BMP2) is one of the key chondrogenic growth factors involved in the cartilage regeneration. However, it also exhibits osteogenic abilities and triggers endochondral ossification. Effective chondrogenesis and inhibition of BMP2-induced osteogenesis and endochondral ossif...

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Detalles Bibliográficos
Autores principales: Liao, Junyi, Hu, Ning, Zhou, Nian, Lin, Liangbo, Zhao, Chen, Yi, Shixiong, Fan, Tingxu, Bao, Wei, Liang, Xi, Chen, Hong, Xu, Wei, Chen, Cheng, Cheng, Qiang, Zeng, Yongming, Si, Weike, Yang, Zhong, Huang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3923876/
https://www.ncbi.nlm.nih.gov/pubmed/24551211
http://dx.doi.org/10.1371/journal.pone.0089025
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author Liao, Junyi
Hu, Ning
Zhou, Nian
Lin, Liangbo
Zhao, Chen
Yi, Shixiong
Fan, Tingxu
Bao, Wei
Liang, Xi
Chen, Hong
Xu, Wei
Chen, Cheng
Cheng, Qiang
Zeng, Yongming
Si, Weike
Yang, Zhong
Huang, Wei
author_facet Liao, Junyi
Hu, Ning
Zhou, Nian
Lin, Liangbo
Zhao, Chen
Yi, Shixiong
Fan, Tingxu
Bao, Wei
Liang, Xi
Chen, Hong
Xu, Wei
Chen, Cheng
Cheng, Qiang
Zeng, Yongming
Si, Weike
Yang, Zhong
Huang, Wei
author_sort Liao, Junyi
collection PubMed
description Bone morphogenetic protein 2 (BMP2) is one of the key chondrogenic growth factors involved in the cartilage regeneration. However, it also exhibits osteogenic abilities and triggers endochondral ossification. Effective chondrogenesis and inhibition of BMP2-induced osteogenesis and endochondral ossification can be achieved by directing the mesenchymal stem cells (MSCs) towards chondrocyte lineage with chodrogenic factors, such as Sox9. Here we investigated the effects of Sox9 on BMP2-induced chondrogenic and osteogenic differentiation of MSCs. We found exogenous overexpression of Sox9 enhanced the BMP2-induced chondrogenic differentiation of MSCs in vitro. Also, it inhibited early and late osteogenic differentiation of MSCs in vitro. Subcutaneous stem cell implantation demonstrated Sox9 potentiated BMP2-induced cartilage formation and inhibited endochondral ossification. Mouse limb cultures indicated that BMP2 and Sox9 acted synergistically to stimulate chondrocytes proliferation, and Sox9 inhibited BMP2-induced chondrocytes hypertrophy and ossification. This study strongly suggests that Sox9 potentiates BMP2-induced MSCs chondrogenic differentiation and cartilage formation, and inhibits BMP2-induced MSCs osteogenic differentiation and endochondral ossification. Thus, exogenous overexpression of Sox9 in BMP2-induced mesenchymal stem cells differentiation may be a new strategy for cartilage tissue engineering.
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spelling pubmed-39238762014-02-18 Sox9 Potentiates BMP2-Induced Chondrogenic Differentiation and Inhibits BMP2-Induced Osteogenic Differentiation Liao, Junyi Hu, Ning Zhou, Nian Lin, Liangbo Zhao, Chen Yi, Shixiong Fan, Tingxu Bao, Wei Liang, Xi Chen, Hong Xu, Wei Chen, Cheng Cheng, Qiang Zeng, Yongming Si, Weike Yang, Zhong Huang, Wei PLoS One Research Article Bone morphogenetic protein 2 (BMP2) is one of the key chondrogenic growth factors involved in the cartilage regeneration. However, it also exhibits osteogenic abilities and triggers endochondral ossification. Effective chondrogenesis and inhibition of BMP2-induced osteogenesis and endochondral ossification can be achieved by directing the mesenchymal stem cells (MSCs) towards chondrocyte lineage with chodrogenic factors, such as Sox9. Here we investigated the effects of Sox9 on BMP2-induced chondrogenic and osteogenic differentiation of MSCs. We found exogenous overexpression of Sox9 enhanced the BMP2-induced chondrogenic differentiation of MSCs in vitro. Also, it inhibited early and late osteogenic differentiation of MSCs in vitro. Subcutaneous stem cell implantation demonstrated Sox9 potentiated BMP2-induced cartilage formation and inhibited endochondral ossification. Mouse limb cultures indicated that BMP2 and Sox9 acted synergistically to stimulate chondrocytes proliferation, and Sox9 inhibited BMP2-induced chondrocytes hypertrophy and ossification. This study strongly suggests that Sox9 potentiates BMP2-induced MSCs chondrogenic differentiation and cartilage formation, and inhibits BMP2-induced MSCs osteogenic differentiation and endochondral ossification. Thus, exogenous overexpression of Sox9 in BMP2-induced mesenchymal stem cells differentiation may be a new strategy for cartilage tissue engineering. Public Library of Science 2014-02-13 /pmc/articles/PMC3923876/ /pubmed/24551211 http://dx.doi.org/10.1371/journal.pone.0089025 Text en © 2014 Liao et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Liao, Junyi
Hu, Ning
Zhou, Nian
Lin, Liangbo
Zhao, Chen
Yi, Shixiong
Fan, Tingxu
Bao, Wei
Liang, Xi
Chen, Hong
Xu, Wei
Chen, Cheng
Cheng, Qiang
Zeng, Yongming
Si, Weike
Yang, Zhong
Huang, Wei
Sox9 Potentiates BMP2-Induced Chondrogenic Differentiation and Inhibits BMP2-Induced Osteogenic Differentiation
title Sox9 Potentiates BMP2-Induced Chondrogenic Differentiation and Inhibits BMP2-Induced Osteogenic Differentiation
title_full Sox9 Potentiates BMP2-Induced Chondrogenic Differentiation and Inhibits BMP2-Induced Osteogenic Differentiation
title_fullStr Sox9 Potentiates BMP2-Induced Chondrogenic Differentiation and Inhibits BMP2-Induced Osteogenic Differentiation
title_full_unstemmed Sox9 Potentiates BMP2-Induced Chondrogenic Differentiation and Inhibits BMP2-Induced Osteogenic Differentiation
title_short Sox9 Potentiates BMP2-Induced Chondrogenic Differentiation and Inhibits BMP2-Induced Osteogenic Differentiation
title_sort sox9 potentiates bmp2-induced chondrogenic differentiation and inhibits bmp2-induced osteogenic differentiation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3923876/
https://www.ncbi.nlm.nih.gov/pubmed/24551211
http://dx.doi.org/10.1371/journal.pone.0089025
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