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Integrins, cadherins and channels in cartilage mechanotransduction: perspectives for future regeneration strategies
Articular cartilage consists of hyaline cartilage, is a major constituent of the human musculoskeletal system and has critical functions in frictionless joint movement and articular homoeostasis. Osteoarthritis (OA) is an inflammatory disease of articular cartilage, which promotes joint degeneration...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8724267/ https://www.ncbi.nlm.nih.gov/pubmed/34702419 http://dx.doi.org/10.1017/erm.2021.16 |
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author | Dieterle, Martin Philipp Husari, Ayman Rolauffs, Bernd Steinberg, Thorsten Tomakidi, Pascal |
author_facet | Dieterle, Martin Philipp Husari, Ayman Rolauffs, Bernd Steinberg, Thorsten Tomakidi, Pascal |
author_sort | Dieterle, Martin Philipp |
collection | PubMed |
description | Articular cartilage consists of hyaline cartilage, is a major constituent of the human musculoskeletal system and has critical functions in frictionless joint movement and articular homoeostasis. Osteoarthritis (OA) is an inflammatory disease of articular cartilage, which promotes joint degeneration. Although it affects millions of people, there are no satisfying therapies that address this disease at the molecular level. Therefore, tissue regeneration approaches aim at modifying chondrocyte biology to mitigate the consequences of OA. This requires appropriate biochemical and biophysical stimulation of cells. Regarding the latter, mechanotransduction of chondrocytes and their precursor cells has become increasingly important over the last few decades. Mechanotransduction is the transformation of external biophysical stimuli into intracellular biochemical signals, involving sensor molecules at the cell surface and intracellular signalling molecules, so-called mechano-sensors and -transducers. These signalling events determine cell behaviour. Mechanotransducing ion channels and gap junctions additionally govern chondrocyte physiology. It is of great scientific and medical interest to induce a specific cell behaviour by controlling these mechanotransduction pathways and to translate this knowledge into regenerative clinical therapies. This review therefore focuses on the mechanotransduction properties of integrins, cadherins and ion channels in cartilaginous tissues to provide perspectives for cartilage regeneration. |
format | Online Article Text |
id | pubmed-8724267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-87242672022-01-14 Integrins, cadherins and channels in cartilage mechanotransduction: perspectives for future regeneration strategies Dieterle, Martin Philipp Husari, Ayman Rolauffs, Bernd Steinberg, Thorsten Tomakidi, Pascal Expert Rev Mol Med Review Articular cartilage consists of hyaline cartilage, is a major constituent of the human musculoskeletal system and has critical functions in frictionless joint movement and articular homoeostasis. Osteoarthritis (OA) is an inflammatory disease of articular cartilage, which promotes joint degeneration. Although it affects millions of people, there are no satisfying therapies that address this disease at the molecular level. Therefore, tissue regeneration approaches aim at modifying chondrocyte biology to mitigate the consequences of OA. This requires appropriate biochemical and biophysical stimulation of cells. Regarding the latter, mechanotransduction of chondrocytes and their precursor cells has become increasingly important over the last few decades. Mechanotransduction is the transformation of external biophysical stimuli into intracellular biochemical signals, involving sensor molecules at the cell surface and intracellular signalling molecules, so-called mechano-sensors and -transducers. These signalling events determine cell behaviour. Mechanotransducing ion channels and gap junctions additionally govern chondrocyte physiology. It is of great scientific and medical interest to induce a specific cell behaviour by controlling these mechanotransduction pathways and to translate this knowledge into regenerative clinical therapies. This review therefore focuses on the mechanotransduction properties of integrins, cadherins and ion channels in cartilaginous tissues to provide perspectives for cartilage regeneration. Cambridge University Press 2021-10-27 /pmc/articles/PMC8724267/ /pubmed/34702419 http://dx.doi.org/10.1017/erm.2021.16 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited. |
spellingShingle | Review Dieterle, Martin Philipp Husari, Ayman Rolauffs, Bernd Steinberg, Thorsten Tomakidi, Pascal Integrins, cadherins and channels in cartilage mechanotransduction: perspectives for future regeneration strategies |
title | Integrins, cadherins and channels in cartilage mechanotransduction: perspectives for future regeneration strategies |
title_full | Integrins, cadherins and channels in cartilage mechanotransduction: perspectives for future regeneration strategies |
title_fullStr | Integrins, cadherins and channels in cartilage mechanotransduction: perspectives for future regeneration strategies |
title_full_unstemmed | Integrins, cadherins and channels in cartilage mechanotransduction: perspectives for future regeneration strategies |
title_short | Integrins, cadherins and channels in cartilage mechanotransduction: perspectives for future regeneration strategies |
title_sort | integrins, cadherins and channels in cartilage mechanotransduction: perspectives for future regeneration strategies |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8724267/ https://www.ncbi.nlm.nih.gov/pubmed/34702419 http://dx.doi.org/10.1017/erm.2021.16 |
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