Bone Marrow MSC Secretome Increases Equine Articular Chondrocyte Collagen Accumulation and Their Migratory Capacities.

acellular therapy cartilage organoids cell secretome chondral defects extracellular vesicles horse in vitro repair mesenchymal stem cells osteoarthritis tissue engineering

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
21 May 2022
Historique:
received: 20 04 2022
revised: 17 05 2022
accepted: 19 05 2022
entrez: 28 5 2022
pubmed: 29 5 2022
medline: 1 6 2022
Statut: epublish

Résumé

Equine osteoarthritis (OA) leads to cartilage degradation with impaired animal well-being, premature cessation of sport activity, and financial losses. Mesenchymal stem cell (MSC)-based therapies are promising for cartilage repair, but face limitations inherent to the cell itself. Soluble mediators and extracellular vesicles (EVs) secreted by MSCs are the alternatives to overcome those limitations while preserving MSC restorative properties. The effect of equine bone marrow MSC secretome on equine articular chondrocytes (eACs) was analyzed with indirect co-culture and/or MSC-conditioned media (CM). The expression of healthy cartilage/OA and proliferation markers was evaluated in eACs (monolayers or organoids). In vitro repair experiments with MSC-CM were made to evaluate the proliferation and migration of eACs. The presence of nanosized EVs in MSC-CM was appraised with nanoparticle tracking assay and transmission electron microscopy. Our results demonstrated that the MSC secretome influences eAC phenotype by increasing cartilage functionality markers and cell migration in a greater way than MSCs, which could delay OA final outcomes. This study makes acellular therapy an appealing strategy to improve equine OA treatments. However, the MSC secretome contains a wide variety of soluble mediators and small EVs, such as exosomes, and further investigation must be performed to understand the mechanisms occurring behind these promising effects.

Identifiants

pubmed: 35628604
pii: ijms23105795
doi: 10.3390/ijms23105795
pmc: PMC9146805
pii:
doi:

Substances chimiques

Culture Media, Conditioned 0
Collagen 9007-34-5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Romain Contentin (R)

Normandie University, Unicaen, Biotargen, F-14000 Caen, France.

Manon Jammes (M)

Normandie University, Unicaen, Biotargen, F-14000 Caen, France.

Bastien Bourdon (B)

Normandie University, Unicaen, Biotargen, F-14000 Caen, France.

Frédéric Cassé (F)

Normandie University, Unicaen, Biotargen, F-14000 Caen, France.

Arnaud Bianchi (A)

Molecular Engineering and Articular Physiopathology (IMoPA), French National Center for Scientific Research (CNRS), Université de Lorraine, F-54000 Nancy, France.

Fabrice Audigié (F)

Center of Imaging and Research on Locomotor Affections on Equines (CIRALE), Unit Under Contract 957 Equine Biomechanics and Locomotor Disorders (USC 957 BPLC), French National Research Institute for Agriculture Food and Environment (INRAE), École Nationale Vétérinaire d'Alfort, F-94700 Maisons-Alfort, France.

Thomas Branly (T)

Normandie University, Unicaen, Biotargen, F-14000 Caen, France.

Émilie Velot (É)

Molecular Engineering and Articular Physiopathology (IMoPA), French National Center for Scientific Research (CNRS), Université de Lorraine, F-54000 Nancy, France.

Philippe Galéra (P)

Normandie University, Unicaen, Biotargen, F-14000 Caen, France.

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Classifications MeSH