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Neural cell adhesion molecule regulates chondrocyte hypertrophy in chondrogenic differentiation and experimental osteoarthritis
Chondrocyte hypertrophy‐like change is an important pathological process of osteoarthritis (OA), but the mechanism remains largely unknown. Neural cell adhesion molecule (NCAM) is highly expressed and involved in the chondrocyte differentiation of mesenchymal stem cells (MSCs). In this study, we fou...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988767/ https://www.ncbi.nlm.nih.gov/pubmed/31742919 http://dx.doi.org/10.1002/sctm.19-0190 |
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author | Cheng, Bin‐Feng Lian, Jun‐Jiang Yang, Hai‐Jie Wang, Lei Yu, Hao‐Heng Bi, Jia‐Jia Gao, Yao‐Xin Chen, Su‐Juan Wang, Mian Feng, Zhi‐Wei |
author_facet | Cheng, Bin‐Feng Lian, Jun‐Jiang Yang, Hai‐Jie Wang, Lei Yu, Hao‐Heng Bi, Jia‐Jia Gao, Yao‐Xin Chen, Su‐Juan Wang, Mian Feng, Zhi‐Wei |
author_sort | Cheng, Bin‐Feng |
collection | PubMed |
description | Chondrocyte hypertrophy‐like change is an important pathological process of osteoarthritis (OA), but the mechanism remains largely unknown. Neural cell adhesion molecule (NCAM) is highly expressed and involved in the chondrocyte differentiation of mesenchymal stem cells (MSCs). In this study, we found that NCAM deficiency accelerates chondrocyte hypertrophy in articular cartilage and growth plate of OA mice. NCAM deficiency leads to hypertrophic chondrocyte differentiation in both murine MSCs and chondrogenic cells, in which extracellular signal‐regulated kinase (ERK) signaling plays an important role. Moreover, NCAM expression is downregulated in an interleukin‐1β‐stimulated OA cellular model and monosodium iodoacetate‐induced OA rats. Overexpression of NCAM substantially inhibits hypertrophic differentiation in the OA cellular model. In conclusion, NCAM could inhibit hypertrophic chondrocyte differentiation of MSCs by inhibiting ERK signaling and reduce chondrocyte hypertrophy in experimental OA model, suggesting the potential utility of NCAM as a novel therapeutic target for alleviating chondrocyte hypertrophy of OA. |
format | Online Article Text |
id | pubmed-6988767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69887672020-02-03 Neural cell adhesion molecule regulates chondrocyte hypertrophy in chondrogenic differentiation and experimental osteoarthritis Cheng, Bin‐Feng Lian, Jun‐Jiang Yang, Hai‐Jie Wang, Lei Yu, Hao‐Heng Bi, Jia‐Jia Gao, Yao‐Xin Chen, Su‐Juan Wang, Mian Feng, Zhi‐Wei Stem Cells Transl Med Tissue‐specific Progenitor and Stem Cells Chondrocyte hypertrophy‐like change is an important pathological process of osteoarthritis (OA), but the mechanism remains largely unknown. Neural cell adhesion molecule (NCAM) is highly expressed and involved in the chondrocyte differentiation of mesenchymal stem cells (MSCs). In this study, we found that NCAM deficiency accelerates chondrocyte hypertrophy in articular cartilage and growth plate of OA mice. NCAM deficiency leads to hypertrophic chondrocyte differentiation in both murine MSCs and chondrogenic cells, in which extracellular signal‐regulated kinase (ERK) signaling plays an important role. Moreover, NCAM expression is downregulated in an interleukin‐1β‐stimulated OA cellular model and monosodium iodoacetate‐induced OA rats. Overexpression of NCAM substantially inhibits hypertrophic differentiation in the OA cellular model. In conclusion, NCAM could inhibit hypertrophic chondrocyte differentiation of MSCs by inhibiting ERK signaling and reduce chondrocyte hypertrophy in experimental OA model, suggesting the potential utility of NCAM as a novel therapeutic target for alleviating chondrocyte hypertrophy of OA. John Wiley & Sons, Inc. 2019-11-19 /pmc/articles/PMC6988767/ /pubmed/31742919 http://dx.doi.org/10.1002/sctm.19-0190 Text en © 2019 The Authors. stem cells translational medicine published by Wiley Periodicals, Inc. on behalf of AlphaMed Press This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Tissue‐specific Progenitor and Stem Cells Cheng, Bin‐Feng Lian, Jun‐Jiang Yang, Hai‐Jie Wang, Lei Yu, Hao‐Heng Bi, Jia‐Jia Gao, Yao‐Xin Chen, Su‐Juan Wang, Mian Feng, Zhi‐Wei Neural cell adhesion molecule regulates chondrocyte hypertrophy in chondrogenic differentiation and experimental osteoarthritis |
title | Neural cell adhesion molecule regulates chondrocyte hypertrophy in chondrogenic differentiation and experimental osteoarthritis |
title_full | Neural cell adhesion molecule regulates chondrocyte hypertrophy in chondrogenic differentiation and experimental osteoarthritis |
title_fullStr | Neural cell adhesion molecule regulates chondrocyte hypertrophy in chondrogenic differentiation and experimental osteoarthritis |
title_full_unstemmed | Neural cell adhesion molecule regulates chondrocyte hypertrophy in chondrogenic differentiation and experimental osteoarthritis |
title_short | Neural cell adhesion molecule regulates chondrocyte hypertrophy in chondrogenic differentiation and experimental osteoarthritis |
title_sort | neural cell adhesion molecule regulates chondrocyte hypertrophy in chondrogenic differentiation and experimental osteoarthritis |
topic | Tissue‐specific Progenitor and Stem Cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988767/ https://www.ncbi.nlm.nih.gov/pubmed/31742919 http://dx.doi.org/10.1002/sctm.19-0190 |
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