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Signaling Pathways in Cartilage Repair

In adult healthy cartilage, chondrocytes are in a quiescent phase characterized by a fine balance between anabolic and catabolic activities. In ageing, degenerative joint diseases and traumatic injuries of cartilage, a loss of homeostatic conditions and an up-regulation of catabolic pathways occur....

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Detalles Bibliográficos
Autores principales: Mariani, Erminia, Pulsatelli, Lia, Facchini, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057753/
https://www.ncbi.nlm.nih.gov/pubmed/24837833
http://dx.doi.org/10.3390/ijms15058667
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author Mariani, Erminia
Pulsatelli, Lia
Facchini, Andrea
author_facet Mariani, Erminia
Pulsatelli, Lia
Facchini, Andrea
author_sort Mariani, Erminia
collection PubMed
description In adult healthy cartilage, chondrocytes are in a quiescent phase characterized by a fine balance between anabolic and catabolic activities. In ageing, degenerative joint diseases and traumatic injuries of cartilage, a loss of homeostatic conditions and an up-regulation of catabolic pathways occur. Since cartilage differentiation and maintenance of homeostasis are finely tuned by a complex network of signaling molecules and biophysical factors, shedding light on these mechanisms appears to be extremely relevant for both the identification of pathogenic key factors, as specific therapeutic targets, and the development of biological approaches for cartilage regeneration. This review will focus on the main signaling pathways that can activate cellular and molecular processes, regulating the functional behavior of cartilage in both physiological and pathological conditions. These networks may be relevant in the crosstalk among joint compartments and increased knowledge in this field may lead to the development of more effective strategies for inducing cartilage repair.
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spelling pubmed-40577532014-06-16 Signaling Pathways in Cartilage Repair Mariani, Erminia Pulsatelli, Lia Facchini, Andrea Int J Mol Sci Review In adult healthy cartilage, chondrocytes are in a quiescent phase characterized by a fine balance between anabolic and catabolic activities. In ageing, degenerative joint diseases and traumatic injuries of cartilage, a loss of homeostatic conditions and an up-regulation of catabolic pathways occur. Since cartilage differentiation and maintenance of homeostasis are finely tuned by a complex network of signaling molecules and biophysical factors, shedding light on these mechanisms appears to be extremely relevant for both the identification of pathogenic key factors, as specific therapeutic targets, and the development of biological approaches for cartilage regeneration. This review will focus on the main signaling pathways that can activate cellular and molecular processes, regulating the functional behavior of cartilage in both physiological and pathological conditions. These networks may be relevant in the crosstalk among joint compartments and increased knowledge in this field may lead to the development of more effective strategies for inducing cartilage repair. Molecular Diversity Preservation International (MDPI) 2014-05-15 /pmc/articles/PMC4057753/ /pubmed/24837833 http://dx.doi.org/10.3390/ijms15058667 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Mariani, Erminia
Pulsatelli, Lia
Facchini, Andrea
Signaling Pathways in Cartilage Repair
title Signaling Pathways in Cartilage Repair
title_full Signaling Pathways in Cartilage Repair
title_fullStr Signaling Pathways in Cartilage Repair
title_full_unstemmed Signaling Pathways in Cartilage Repair
title_short Signaling Pathways in Cartilage Repair
title_sort signaling pathways in cartilage repair
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057753/
https://www.ncbi.nlm.nih.gov/pubmed/24837833
http://dx.doi.org/10.3390/ijms15058667
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