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Age-dependent alteration of TGF-β signalling in osteoarthritis

Osteoarthritis (OA) is a disease of articular cartilage, with aging as the main risk factor. In OA, changes in chondrocytes lead to the autolytic destruction of cartilage. Transforming growth factor-β has recently been demonstrated to signal not only via activin receptor-like kinase 5 (ALK5)-induced...

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Autores principales: van der Kraan, Peter M., Goumans, Marie-José, Blaney Davidson, Esmeralda, ten Dijke, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3250613/
https://www.ncbi.nlm.nih.gov/pubmed/21638205
http://dx.doi.org/10.1007/s00441-011-1194-6
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author van der Kraan, Peter M.
Goumans, Marie-José
Blaney Davidson, Esmeralda
ten Dijke, Peter
author_facet van der Kraan, Peter M.
Goumans, Marie-José
Blaney Davidson, Esmeralda
ten Dijke, Peter
author_sort van der Kraan, Peter M.
collection PubMed
description Osteoarthritis (OA) is a disease of articular cartilage, with aging as the main risk factor. In OA, changes in chondrocytes lead to the autolytic destruction of cartilage. Transforming growth factor-β has recently been demonstrated to signal not only via activin receptor-like kinase 5 (ALK5)-induced Smad2/3 phosphorylation, but also via ALK1-induced Smad1/5/8 phosphorylation in articular cartilage. In aging cartilage and experimental OA, the ratio ALK1/ALK5 has been found to be increased, and the expression of ALK1 is correlated with matrix metalloproteinase-13 expression. The age-dependent shift towards Smad1/5/8 signalling might trigger the differentiation of articular chondrocytes with an autolytic phenotype.
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spelling pubmed-32506132012-01-11 Age-dependent alteration of TGF-β signalling in osteoarthritis van der Kraan, Peter M. Goumans, Marie-José Blaney Davidson, Esmeralda ten Dijke, Peter Cell Tissue Res Review Osteoarthritis (OA) is a disease of articular cartilage, with aging as the main risk factor. In OA, changes in chondrocytes lead to the autolytic destruction of cartilage. Transforming growth factor-β has recently been demonstrated to signal not only via activin receptor-like kinase 5 (ALK5)-induced Smad2/3 phosphorylation, but also via ALK1-induced Smad1/5/8 phosphorylation in articular cartilage. In aging cartilage and experimental OA, the ratio ALK1/ALK5 has been found to be increased, and the expression of ALK1 is correlated with matrix metalloproteinase-13 expression. The age-dependent shift towards Smad1/5/8 signalling might trigger the differentiation of articular chondrocytes with an autolytic phenotype. Springer-Verlag 2011-06-04 2012 /pmc/articles/PMC3250613/ /pubmed/21638205 http://dx.doi.org/10.1007/s00441-011-1194-6 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Review
van der Kraan, Peter M.
Goumans, Marie-José
Blaney Davidson, Esmeralda
ten Dijke, Peter
Age-dependent alteration of TGF-β signalling in osteoarthritis
title Age-dependent alteration of TGF-β signalling in osteoarthritis
title_full Age-dependent alteration of TGF-β signalling in osteoarthritis
title_fullStr Age-dependent alteration of TGF-β signalling in osteoarthritis
title_full_unstemmed Age-dependent alteration of TGF-β signalling in osteoarthritis
title_short Age-dependent alteration of TGF-β signalling in osteoarthritis
title_sort age-dependent alteration of tgf-β signalling in osteoarthritis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3250613/
https://www.ncbi.nlm.nih.gov/pubmed/21638205
http://dx.doi.org/10.1007/s00441-011-1194-6
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