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Equine osteoarthritis: Strategies to enhance mesenchymal stromal cell-based acellular therapies
Osteoarthritis (OA) is a degenerative disease that eventually leads to the complete degradation of articular cartilage. Articular cartilage has limited intrinsic capacity for self-repair and, to date, there is no curative treatment for OA. Humans and horses have a similar articular cartilage and OA...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950114/ https://www.ncbi.nlm.nih.gov/pubmed/36846261 http://dx.doi.org/10.3389/fvets.2023.1115774 |
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author | Jammes, Manon Contentin, Romain Cassé, Frédéric Galéra, Philippe |
author_facet | Jammes, Manon Contentin, Romain Cassé, Frédéric Galéra, Philippe |
author_sort | Jammes, Manon |
collection | PubMed |
description | Osteoarthritis (OA) is a degenerative disease that eventually leads to the complete degradation of articular cartilage. Articular cartilage has limited intrinsic capacity for self-repair and, to date, there is no curative treatment for OA. Humans and horses have a similar articular cartilage and OA etiology. Thus, in the context of a One Health approach, progress in the treatment of equine OA can help improve horse health and can also constitute preclinical studies for human medicine. Furthermore, equine OA affects horse welfare and leads to significant financial losses in the equine industry. In the last few years, the immunomodulatory and cartilage regenerative potentials of mesenchymal stromal cells (MSCs) have been demonstrated, but have also raised several concerns. However, most of MSC therapeutic properties are contained in their secretome, particularly in their extracellular vesicles (EVs), a promising avenue for acellular therapy. From tissue origin to in vitro culture methods, various aspects must be taken into consideration to optimize MSC secretome potential for OA treatment. Immunomodulatory and regenerative properties of MSCs can also be enhanced by recreating a pro-inflammatory environment to mimic an in vivo pathological setting, but more unusual methods also deserve to be investigated. Altogether, these strategies hold substantial potential for the development of MSC secretome-based therapies suitable for OA management. The aim of this mini review is to survey the most recent advances on MSC secretome research with regard to equine OA. |
format | Online Article Text |
id | pubmed-9950114 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99501142023-02-25 Equine osteoarthritis: Strategies to enhance mesenchymal stromal cell-based acellular therapies Jammes, Manon Contentin, Romain Cassé, Frédéric Galéra, Philippe Front Vet Sci Veterinary Science Osteoarthritis (OA) is a degenerative disease that eventually leads to the complete degradation of articular cartilage. Articular cartilage has limited intrinsic capacity for self-repair and, to date, there is no curative treatment for OA. Humans and horses have a similar articular cartilage and OA etiology. Thus, in the context of a One Health approach, progress in the treatment of equine OA can help improve horse health and can also constitute preclinical studies for human medicine. Furthermore, equine OA affects horse welfare and leads to significant financial losses in the equine industry. In the last few years, the immunomodulatory and cartilage regenerative potentials of mesenchymal stromal cells (MSCs) have been demonstrated, but have also raised several concerns. However, most of MSC therapeutic properties are contained in their secretome, particularly in their extracellular vesicles (EVs), a promising avenue for acellular therapy. From tissue origin to in vitro culture methods, various aspects must be taken into consideration to optimize MSC secretome potential for OA treatment. Immunomodulatory and regenerative properties of MSCs can also be enhanced by recreating a pro-inflammatory environment to mimic an in vivo pathological setting, but more unusual methods also deserve to be investigated. Altogether, these strategies hold substantial potential for the development of MSC secretome-based therapies suitable for OA management. The aim of this mini review is to survey the most recent advances on MSC secretome research with regard to equine OA. Frontiers Media S.A. 2023-02-10 /pmc/articles/PMC9950114/ /pubmed/36846261 http://dx.doi.org/10.3389/fvets.2023.1115774 Text en Copyright © 2023 Jammes, Contentin, Cassé and Galéra. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Veterinary Science Jammes, Manon Contentin, Romain Cassé, Frédéric Galéra, Philippe Equine osteoarthritis: Strategies to enhance mesenchymal stromal cell-based acellular therapies |
title | Equine osteoarthritis: Strategies to enhance mesenchymal stromal cell-based acellular therapies |
title_full | Equine osteoarthritis: Strategies to enhance mesenchymal stromal cell-based acellular therapies |
title_fullStr | Equine osteoarthritis: Strategies to enhance mesenchymal stromal cell-based acellular therapies |
title_full_unstemmed | Equine osteoarthritis: Strategies to enhance mesenchymal stromal cell-based acellular therapies |
title_short | Equine osteoarthritis: Strategies to enhance mesenchymal stromal cell-based acellular therapies |
title_sort | equine osteoarthritis: strategies to enhance mesenchymal stromal cell-based acellular therapies |
topic | Veterinary Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950114/ https://www.ncbi.nlm.nih.gov/pubmed/36846261 http://dx.doi.org/10.3389/fvets.2023.1115774 |
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