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Disorganization of chondrocyte columns in the growth plate does not aggravate experimental osteoarthritis in mice

Osteoarthritis (OA) is a multifactorial joint disease mainly affecting articular cartilage (AC) with a relevant biomechanical component. During endochondral ossification growth plate (GP) chondrocytes arrange in columns. GPs do not ossify in skeletally mature rodents. In neonatal mice, an altered jo...

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Autores principales: Lamuedra, Ana, Gratal, Paula, Calatrava, Lucía, Ruiz-Perez, Víctor Luis, Largo, Raquel, Herrero-Beaumont, Gabriel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329885/
https://www.ncbi.nlm.nih.gov/pubmed/32612184
http://dx.doi.org/10.1038/s41598-020-67518-0
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author Lamuedra, Ana
Gratal, Paula
Calatrava, Lucía
Ruiz-Perez, Víctor Luis
Largo, Raquel
Herrero-Beaumont, Gabriel
author_facet Lamuedra, Ana
Gratal, Paula
Calatrava, Lucía
Ruiz-Perez, Víctor Luis
Largo, Raquel
Herrero-Beaumont, Gabriel
author_sort Lamuedra, Ana
collection PubMed
description Osteoarthritis (OA) is a multifactorial joint disease mainly affecting articular cartilage (AC) with a relevant biomechanical component. During endochondral ossification growth plate (GP) chondrocytes arrange in columns. GPs do not ossify in skeletally mature rodents. In neonatal mice, an altered joint loading induces GP chondrocyte disorganization. We aimed to study whether experimental OA involves GP disorganization in adult mice and to assess if it may have additional detrimental effects on AC damage. Knee OA was induced by destabilization of the medial meniscus (DMM) in wild-type (WT) adult mice, and in Tamoxifen-inducible Ellis-van-Creveld syndrome protein (Evc) knockouts (Evc(cKO)), used as a model of GP disorganization due to Hedgehog signalling disruption. Chondrocyte column arrangement was assessed in the tibial GP and expressed as Column Index (CI). Both DMM-operated WT mice and non-operated-Evc(cKO) showed a decreased CI, indicating GP chondrocyte column disarrangement, although in the latter, it was not associated to AC damage. The most severe GP chondrocyte disorganization occurred in DMM-Evc(cKO) mice, in comparison to the other groups. However, this altered GP structure in DMM-Evc(cKO) mice did not exacerbate AC damage. Further studies are needed to confirm the lack of interference of GP alterations on the analysis of AC employing OA mice.
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spelling pubmed-73298852020-07-06 Disorganization of chondrocyte columns in the growth plate does not aggravate experimental osteoarthritis in mice Lamuedra, Ana Gratal, Paula Calatrava, Lucía Ruiz-Perez, Víctor Luis Largo, Raquel Herrero-Beaumont, Gabriel Sci Rep Article Osteoarthritis (OA) is a multifactorial joint disease mainly affecting articular cartilage (AC) with a relevant biomechanical component. During endochondral ossification growth plate (GP) chondrocytes arrange in columns. GPs do not ossify in skeletally mature rodents. In neonatal mice, an altered joint loading induces GP chondrocyte disorganization. We aimed to study whether experimental OA involves GP disorganization in adult mice and to assess if it may have additional detrimental effects on AC damage. Knee OA was induced by destabilization of the medial meniscus (DMM) in wild-type (WT) adult mice, and in Tamoxifen-inducible Ellis-van-Creveld syndrome protein (Evc) knockouts (Evc(cKO)), used as a model of GP disorganization due to Hedgehog signalling disruption. Chondrocyte column arrangement was assessed in the tibial GP and expressed as Column Index (CI). Both DMM-operated WT mice and non-operated-Evc(cKO) showed a decreased CI, indicating GP chondrocyte column disarrangement, although in the latter, it was not associated to AC damage. The most severe GP chondrocyte disorganization occurred in DMM-Evc(cKO) mice, in comparison to the other groups. However, this altered GP structure in DMM-Evc(cKO) mice did not exacerbate AC damage. Further studies are needed to confirm the lack of interference of GP alterations on the analysis of AC employing OA mice. Nature Publishing Group UK 2020-07-01 /pmc/articles/PMC7329885/ /pubmed/32612184 http://dx.doi.org/10.1038/s41598-020-67518-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lamuedra, Ana
Gratal, Paula
Calatrava, Lucía
Ruiz-Perez, Víctor Luis
Largo, Raquel
Herrero-Beaumont, Gabriel
Disorganization of chondrocyte columns in the growth plate does not aggravate experimental osteoarthritis in mice
title Disorganization of chondrocyte columns in the growth plate does not aggravate experimental osteoarthritis in mice
title_full Disorganization of chondrocyte columns in the growth plate does not aggravate experimental osteoarthritis in mice
title_fullStr Disorganization of chondrocyte columns in the growth plate does not aggravate experimental osteoarthritis in mice
title_full_unstemmed Disorganization of chondrocyte columns in the growth plate does not aggravate experimental osteoarthritis in mice
title_short Disorganization of chondrocyte columns in the growth plate does not aggravate experimental osteoarthritis in mice
title_sort disorganization of chondrocyte columns in the growth plate does not aggravate experimental osteoarthritis in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329885/
https://www.ncbi.nlm.nih.gov/pubmed/32612184
http://dx.doi.org/10.1038/s41598-020-67518-0
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