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Human Osteochondral Explants as an Ex Vivo Model of Osteoarthritis for the Assessment of a Novel Class of Orthobiologics

Osteoarthritis (OA) is a highly prevalent joint disease still lacking effective treatments. Its multifactorial etiology hampers the development of relevant preclinical models to evaluate innovative therapeutic solutions. In the last decade, the potential of Mesenchymal Stem Cell (MSC) secretome, or...

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Autores principales: Giannasi, Chiara, Mangiavini, Laura, Niada, Stefania, Colombo, Andrea, Della Morte, Elena, Vismara, Valeria, Ambrosanio, Andrea, Savadori, Paolo, Casati, Sara, Peretti, Giuseppe M., Brini, Anna Teresa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9229444/
https://www.ncbi.nlm.nih.gov/pubmed/35745803
http://dx.doi.org/10.3390/pharmaceutics14061231
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author Giannasi, Chiara
Mangiavini, Laura
Niada, Stefania
Colombo, Andrea
Della Morte, Elena
Vismara, Valeria
Ambrosanio, Andrea
Savadori, Paolo
Casati, Sara
Peretti, Giuseppe M.
Brini, Anna Teresa
author_facet Giannasi, Chiara
Mangiavini, Laura
Niada, Stefania
Colombo, Andrea
Della Morte, Elena
Vismara, Valeria
Ambrosanio, Andrea
Savadori, Paolo
Casati, Sara
Peretti, Giuseppe M.
Brini, Anna Teresa
author_sort Giannasi, Chiara
collection PubMed
description Osteoarthritis (OA) is a highly prevalent joint disease still lacking effective treatments. Its multifactorial etiology hampers the development of relevant preclinical models to evaluate innovative therapeutic solutions. In the last decade, the potential of Mesenchymal Stem Cell (MSC) secretome, or conditioned medium (CM), has emerged as an alternative to cell therapy. Here, we investigated the effects of the CM from adipose MSCs (ASCs), accounting for both soluble factors and extracellular vesicles, on human osteochondral explants. Biopsies, isolated from total knee replacement surgery, were cultured without additional treatment or with the CM from 10(6) ASCs, both in the absence and in the presence of 10 ng/mL TNFα. Tissue viability and several OA-related hallmarks were monitored at 1, 3 and 6 days. Specimen viability was maintained over culture. After 3 days, TNFα induced the enhancement of matrix metalloproteinase activity and glycosaminoglycan release, both efficiently counteracted by CM. The screening of inflammatory lipids, proteases and cytokines outlined interesting modulations, driving the attention to new players in the OA process. Here, we confirmed the promising beneficial action of ASC secretome in the OA context and profiled several bioactive factors involved in its progression, in the perspective of accelerating an answer to its unmet clinical needs.
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spelling pubmed-92294442022-06-25 Human Osteochondral Explants as an Ex Vivo Model of Osteoarthritis for the Assessment of a Novel Class of Orthobiologics Giannasi, Chiara Mangiavini, Laura Niada, Stefania Colombo, Andrea Della Morte, Elena Vismara, Valeria Ambrosanio, Andrea Savadori, Paolo Casati, Sara Peretti, Giuseppe M. Brini, Anna Teresa Pharmaceutics Article Osteoarthritis (OA) is a highly prevalent joint disease still lacking effective treatments. Its multifactorial etiology hampers the development of relevant preclinical models to evaluate innovative therapeutic solutions. In the last decade, the potential of Mesenchymal Stem Cell (MSC) secretome, or conditioned medium (CM), has emerged as an alternative to cell therapy. Here, we investigated the effects of the CM from adipose MSCs (ASCs), accounting for both soluble factors and extracellular vesicles, on human osteochondral explants. Biopsies, isolated from total knee replacement surgery, were cultured without additional treatment or with the CM from 10(6) ASCs, both in the absence and in the presence of 10 ng/mL TNFα. Tissue viability and several OA-related hallmarks were monitored at 1, 3 and 6 days. Specimen viability was maintained over culture. After 3 days, TNFα induced the enhancement of matrix metalloproteinase activity and glycosaminoglycan release, both efficiently counteracted by CM. The screening of inflammatory lipids, proteases and cytokines outlined interesting modulations, driving the attention to new players in the OA process. Here, we confirmed the promising beneficial action of ASC secretome in the OA context and profiled several bioactive factors involved in its progression, in the perspective of accelerating an answer to its unmet clinical needs. MDPI 2022-06-10 /pmc/articles/PMC9229444/ /pubmed/35745803 http://dx.doi.org/10.3390/pharmaceutics14061231 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Giannasi, Chiara
Mangiavini, Laura
Niada, Stefania
Colombo, Andrea
Della Morte, Elena
Vismara, Valeria
Ambrosanio, Andrea
Savadori, Paolo
Casati, Sara
Peretti, Giuseppe M.
Brini, Anna Teresa
Human Osteochondral Explants as an Ex Vivo Model of Osteoarthritis for the Assessment of a Novel Class of Orthobiologics
title Human Osteochondral Explants as an Ex Vivo Model of Osteoarthritis for the Assessment of a Novel Class of Orthobiologics
title_full Human Osteochondral Explants as an Ex Vivo Model of Osteoarthritis for the Assessment of a Novel Class of Orthobiologics
title_fullStr Human Osteochondral Explants as an Ex Vivo Model of Osteoarthritis for the Assessment of a Novel Class of Orthobiologics
title_full_unstemmed Human Osteochondral Explants as an Ex Vivo Model of Osteoarthritis for the Assessment of a Novel Class of Orthobiologics
title_short Human Osteochondral Explants as an Ex Vivo Model of Osteoarthritis for the Assessment of a Novel Class of Orthobiologics
title_sort human osteochondral explants as an ex vivo model of osteoarthritis for the assessment of a novel class of orthobiologics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9229444/
https://www.ncbi.nlm.nih.gov/pubmed/35745803
http://dx.doi.org/10.3390/pharmaceutics14061231
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