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Discerning the spatio-temporal disease patterns of surgically induced OA mouse models
Osteoarthritis (OA) is the most common cause of disability in ageing societies, with no effective therapies available to date. Two preclinical models are widely used to validate novel OA interventions (MCL-MM and DMM). Our aim is to discern disease dynamics in these models to provide a clear timelin...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459499/ https://www.ncbi.nlm.nih.gov/pubmed/30973882 http://dx.doi.org/10.1371/journal.pone.0213734 |
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author | Haase, Tobias Sunkara, Vikram Kohl, Benjamin Meier, Carola Bußmann, Patricia Becker, Jessica Jagielski, Michal von Kleist, Max Ertel, Wolfgang |
author_facet | Haase, Tobias Sunkara, Vikram Kohl, Benjamin Meier, Carola Bußmann, Patricia Becker, Jessica Jagielski, Michal von Kleist, Max Ertel, Wolfgang |
author_sort | Haase, Tobias |
collection | PubMed |
description | Osteoarthritis (OA) is the most common cause of disability in ageing societies, with no effective therapies available to date. Two preclinical models are widely used to validate novel OA interventions (MCL-MM and DMM). Our aim is to discern disease dynamics in these models to provide a clear timeline in which various pathological changes occur. OA was surgically induced in mice by destabilisation of the medial meniscus. Analysis of OA progression revealed that the intensity and duration of chondrocyte loss and cartilage lesion formation were significantly different in MCL-MM vs DMM. Firstly, apoptosis was seen prior to week two and was narrowly restricted to the weight bearing area. Four weeks post injury the magnitude of apoptosis led to a 40–60% reduction of chondrocytes in the non-calcified zone. Secondly, the progression of cell loss preceded the structural changes of the cartilage spatio-temporally. Lastly, while proteoglycan loss was similar in both models, collagen type II degradation only occurred more prominently in MCL-MM. Dynamics of chondrocyte loss and lesion formation in preclinical models has important implications for validating new therapeutic strategies. Our work could be helpful in assessing the feasibility and expected response of the DMM- and the MCL-MM models to chondrocyte mediated therapies. |
format | Online Article Text |
id | pubmed-6459499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-64594992019-05-03 Discerning the spatio-temporal disease patterns of surgically induced OA mouse models Haase, Tobias Sunkara, Vikram Kohl, Benjamin Meier, Carola Bußmann, Patricia Becker, Jessica Jagielski, Michal von Kleist, Max Ertel, Wolfgang PLoS One Research Article Osteoarthritis (OA) is the most common cause of disability in ageing societies, with no effective therapies available to date. Two preclinical models are widely used to validate novel OA interventions (MCL-MM and DMM). Our aim is to discern disease dynamics in these models to provide a clear timeline in which various pathological changes occur. OA was surgically induced in mice by destabilisation of the medial meniscus. Analysis of OA progression revealed that the intensity and duration of chondrocyte loss and cartilage lesion formation were significantly different in MCL-MM vs DMM. Firstly, apoptosis was seen prior to week two and was narrowly restricted to the weight bearing area. Four weeks post injury the magnitude of apoptosis led to a 40–60% reduction of chondrocytes in the non-calcified zone. Secondly, the progression of cell loss preceded the structural changes of the cartilage spatio-temporally. Lastly, while proteoglycan loss was similar in both models, collagen type II degradation only occurred more prominently in MCL-MM. Dynamics of chondrocyte loss and lesion formation in preclinical models has important implications for validating new therapeutic strategies. Our work could be helpful in assessing the feasibility and expected response of the DMM- and the MCL-MM models to chondrocyte mediated therapies. Public Library of Science 2019-04-11 /pmc/articles/PMC6459499/ /pubmed/30973882 http://dx.doi.org/10.1371/journal.pone.0213734 Text en © 2019 Haase et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Haase, Tobias Sunkara, Vikram Kohl, Benjamin Meier, Carola Bußmann, Patricia Becker, Jessica Jagielski, Michal von Kleist, Max Ertel, Wolfgang Discerning the spatio-temporal disease patterns of surgically induced OA mouse models |
title | Discerning the spatio-temporal disease patterns of surgically induced OA mouse models |
title_full | Discerning the spatio-temporal disease patterns of surgically induced OA mouse models |
title_fullStr | Discerning the spatio-temporal disease patterns of surgically induced OA mouse models |
title_full_unstemmed | Discerning the spatio-temporal disease patterns of surgically induced OA mouse models |
title_short | Discerning the spatio-temporal disease patterns of surgically induced OA mouse models |
title_sort | discerning the spatio-temporal disease patterns of surgically induced oa mouse models |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459499/ https://www.ncbi.nlm.nih.gov/pubmed/30973882 http://dx.doi.org/10.1371/journal.pone.0213734 |
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