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TGFβ/BMP Signaling Pathway in Cartilage Homeostasis
Cartilage homeostasis is governed by articular chondrocytes via their ability to modulate extracellular matrix production and degradation. In turn, chondrocyte activity is regulated by growth factors such as those of the transforming growth factor β (TGFβ) family. Members of this family include the...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769927/ https://www.ncbi.nlm.nih.gov/pubmed/31450621 http://dx.doi.org/10.3390/cells8090969 |
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author | Thielen, Nathalie G.M. van der Kraan, Peter M. van Caam, Arjan P.M. |
author_facet | Thielen, Nathalie G.M. van der Kraan, Peter M. van Caam, Arjan P.M. |
author_sort | Thielen, Nathalie G.M. |
collection | PubMed |
description | Cartilage homeostasis is governed by articular chondrocytes via their ability to modulate extracellular matrix production and degradation. In turn, chondrocyte activity is regulated by growth factors such as those of the transforming growth factor β (TGFβ) family. Members of this family include the TGFβs, bone morphogenetic proteins (BMPs), and growth and differentiation factors (GDFs). Signaling by this protein family uniquely activates SMAD-dependent signaling and transcription but also activates SMAD-independent signaling via MAPKs such as ERK and TAK1. This review will address the pivotal role of the TGFβ family in cartilage biology by listing several TGFβ family members and describing their signaling and importance for cartilage maintenance. In addition, it is discussed how (pathological) processes such as aging, mechanical stress, and inflammation contribute to altered TGFβ family signaling, leading to disturbed cartilage metabolism and disease. |
format | Online Article Text |
id | pubmed-6769927 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67699272019-10-30 TGFβ/BMP Signaling Pathway in Cartilage Homeostasis Thielen, Nathalie G.M. van der Kraan, Peter M. van Caam, Arjan P.M. Cells Review Cartilage homeostasis is governed by articular chondrocytes via their ability to modulate extracellular matrix production and degradation. In turn, chondrocyte activity is regulated by growth factors such as those of the transforming growth factor β (TGFβ) family. Members of this family include the TGFβs, bone morphogenetic proteins (BMPs), and growth and differentiation factors (GDFs). Signaling by this protein family uniquely activates SMAD-dependent signaling and transcription but also activates SMAD-independent signaling via MAPKs such as ERK and TAK1. This review will address the pivotal role of the TGFβ family in cartilage biology by listing several TGFβ family members and describing their signaling and importance for cartilage maintenance. In addition, it is discussed how (pathological) processes such as aging, mechanical stress, and inflammation contribute to altered TGFβ family signaling, leading to disturbed cartilage metabolism and disease. MDPI 2019-08-24 /pmc/articles/PMC6769927/ /pubmed/31450621 http://dx.doi.org/10.3390/cells8090969 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Thielen, Nathalie G.M. van der Kraan, Peter M. van Caam, Arjan P.M. TGFβ/BMP Signaling Pathway in Cartilage Homeostasis |
title | TGFβ/BMP Signaling Pathway in Cartilage Homeostasis |
title_full | TGFβ/BMP Signaling Pathway in Cartilage Homeostasis |
title_fullStr | TGFβ/BMP Signaling Pathway in Cartilage Homeostasis |
title_full_unstemmed | TGFβ/BMP Signaling Pathway in Cartilage Homeostasis |
title_short | TGFβ/BMP Signaling Pathway in Cartilage Homeostasis |
title_sort | tgfβ/bmp signaling pathway in cartilage homeostasis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769927/ https://www.ncbi.nlm.nih.gov/pubmed/31450621 http://dx.doi.org/10.3390/cells8090969 |
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