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Naked mole‐rats are extremely resistant to post‐traumatic osteoarthritis

Osteoarthritis (OA) is the most prevalent disabling disease, affecting quality of life and contributing to morbidity, particularly during aging. Current treatments for OA are limited to palliation: pain management and surgery for end‐stage disease. Innovative approaches and animal models are needed...

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Autores principales: Taguchi, Taketo, Kotelsky, Alexander, Takasugi, Masaki, Chang, Martin, Ke, Zhonghe, Betancourt, Megan, Buckley, Mark R., Zuscik, Michael, Seluanov, Andrei, Gorbunova, Vera
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7681040/
https://www.ncbi.nlm.nih.gov/pubmed/33112509
http://dx.doi.org/10.1111/acel.13255
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author Taguchi, Taketo
Kotelsky, Alexander
Takasugi, Masaki
Chang, Martin
Ke, Zhonghe
Betancourt, Megan
Buckley, Mark R.
Zuscik, Michael
Seluanov, Andrei
Gorbunova, Vera
author_facet Taguchi, Taketo
Kotelsky, Alexander
Takasugi, Masaki
Chang, Martin
Ke, Zhonghe
Betancourt, Megan
Buckley, Mark R.
Zuscik, Michael
Seluanov, Andrei
Gorbunova, Vera
author_sort Taguchi, Taketo
collection PubMed
description Osteoarthritis (OA) is the most prevalent disabling disease, affecting quality of life and contributing to morbidity, particularly during aging. Current treatments for OA are limited to palliation: pain management and surgery for end‐stage disease. Innovative approaches and animal models are needed to develop curative treatments for OA. Here, we investigated the naked mole‐rat (NMR) as a potential model of OA resistance. NMR is a small rodent with the maximum lifespan of over 30 years, resistant to a wide range of age‐related diseases. NMR tissues accumulate large quantities of unique, very high molecular weight, hyaluronan (HA). HA is a major component of cartilage and synovial fluid. Importantly, both HA molecular weight and cartilage stiffness decline with age and progression of OA. As increased polymer length is known to result in stiffer material, we hypothesized that NMR high molecular weight HA contributes to stiffer cartilage. Our analysis of biomechanical properties of NMR cartilage revealed that it is significantly stiffer than mouse cartilage. Furthermore, NMR chondrocytes were highly resistant to traumatic damage. In vivo experiments using an injury‐induced model of OA revealed that NMRs were highly resistant to OA. While similarly treated mice developed severe cartilage degeneration, NMRs did not show any signs of OA. Our study shows that NMRs are remarkably resistant to OA, and this resistance is likely conferred by high molecular weight HA. This work suggests that NMR is a useful model to study OA resistance and NMR high molecular weight HA may hold therapeutic potential for OA treatment.
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spelling pubmed-76810402020-11-27 Naked mole‐rats are extremely resistant to post‐traumatic osteoarthritis Taguchi, Taketo Kotelsky, Alexander Takasugi, Masaki Chang, Martin Ke, Zhonghe Betancourt, Megan Buckley, Mark R. Zuscik, Michael Seluanov, Andrei Gorbunova, Vera Aging Cell Original Articles Osteoarthritis (OA) is the most prevalent disabling disease, affecting quality of life and contributing to morbidity, particularly during aging. Current treatments for OA are limited to palliation: pain management and surgery for end‐stage disease. Innovative approaches and animal models are needed to develop curative treatments for OA. Here, we investigated the naked mole‐rat (NMR) as a potential model of OA resistance. NMR is a small rodent with the maximum lifespan of over 30 years, resistant to a wide range of age‐related diseases. NMR tissues accumulate large quantities of unique, very high molecular weight, hyaluronan (HA). HA is a major component of cartilage and synovial fluid. Importantly, both HA molecular weight and cartilage stiffness decline with age and progression of OA. As increased polymer length is known to result in stiffer material, we hypothesized that NMR high molecular weight HA contributes to stiffer cartilage. Our analysis of biomechanical properties of NMR cartilage revealed that it is significantly stiffer than mouse cartilage. Furthermore, NMR chondrocytes were highly resistant to traumatic damage. In vivo experiments using an injury‐induced model of OA revealed that NMRs were highly resistant to OA. While similarly treated mice developed severe cartilage degeneration, NMRs did not show any signs of OA. Our study shows that NMRs are remarkably resistant to OA, and this resistance is likely conferred by high molecular weight HA. This work suggests that NMR is a useful model to study OA resistance and NMR high molecular weight HA may hold therapeutic potential for OA treatment. John Wiley and Sons Inc. 2020-10-28 2020-11 /pmc/articles/PMC7681040/ /pubmed/33112509 http://dx.doi.org/10.1111/acel.13255 Text en © 2020 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Taguchi, Taketo
Kotelsky, Alexander
Takasugi, Masaki
Chang, Martin
Ke, Zhonghe
Betancourt, Megan
Buckley, Mark R.
Zuscik, Michael
Seluanov, Andrei
Gorbunova, Vera
Naked mole‐rats are extremely resistant to post‐traumatic osteoarthritis
title Naked mole‐rats are extremely resistant to post‐traumatic osteoarthritis
title_full Naked mole‐rats are extremely resistant to post‐traumatic osteoarthritis
title_fullStr Naked mole‐rats are extremely resistant to post‐traumatic osteoarthritis
title_full_unstemmed Naked mole‐rats are extremely resistant to post‐traumatic osteoarthritis
title_short Naked mole‐rats are extremely resistant to post‐traumatic osteoarthritis
title_sort naked mole‐rats are extremely resistant to post‐traumatic osteoarthritis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7681040/
https://www.ncbi.nlm.nih.gov/pubmed/33112509
http://dx.doi.org/10.1111/acel.13255
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