Mesenchymal stem/stromal cells-derived extracellular vesicles as a potentially more beneficial therapeutic strategy than MSC-based treatment in a mild metabolic osteoarthritis model
Warmink, Kelly; Rios, Jaqueline L; Varderidou-Minasian, Suzy; Torres-Torrillas, Marta; van Valkengoed, Devin R; Versteeg, Sabine; Eijkelkamp, Niels; Weinans, Harrie; Korthagen, Nicoline M; Lorenowicz, Magdalena J
(2023) Stem cell research & therapy, volume 14, issue 1
(Article)
Abstract
BACKGROUND: Mesenchymal stromal/stem cells (MSCs) and MSC-derived extracellular vesicles (MSC-EVs) hold promise as a disease modifying treatment in osteoarthritis (OA). Obesity, and its associated inflammation, contribute to OA development and metabolic OA represents a specific and significant group of the OA patient population. Given their immunomodulatory properties, MSC and MSC-EVs
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are especially interesting for this group of patients as a therapeutic option. Here, we were the first to compare the therapeutic efficacy of MSCs and MSC-EVs in a mild OA model taking these metabolic aspects into consideration. METHODS: Male Wistar-Han rats (Crl:WI(Han) (n = 36) were fed a high fat diet for 24 weeks, with unilateral induction of OA by groove surgery after 12 weeks. Eight days after surgery rats were randomized in three treatment groups receiving MSCs, MSC-EVs or vehicle injection. Pain-associated behavior, joint degeneration, and local and systemic inflammation were measured. RESULTS: We demonstrated that despite not having a significant therapeutic effect, MSC-EV treatment results in lower cartilage degeneration, less pain behaviour, osteophytosis and joint inflammation, than MSC treatment. Suggesting that MSC-EVs could be a more promising therapeutic strategy than MSCs in this mild metabolic OA model. CONCLUSION: In summary, we find that MSC treatment has negative effects on the joint in metabolic mild OA. This is an essential finding for the significant group of patients with metabolic OA phenotype, and might help to understand why clinical translation of MSC treatment shows varying therapeutic efficacy thus far. Our results also suggest that MSC-EV-based treatment might be a promising option for these patients, however MSC-EV therapeutic efficacy will need improvement.
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Keywords: Cartilage regeneration, Extracellular vesicles, Inflammation, Mesenchymal stem/stromal cells, Osteoarthritis, Rat high fat diet groove model, Molecular Medicine, Biochemistry, Genetics and Molecular Biology (miscellaneous), Medicine (miscellaneous), Cell Biology
ISSN: 1757-6512
Publisher: BioMed Central
Note: Funding Information: We would like to thank MultiPlex Core Facility (Laboratory of Translational Immunology, University Medical Center Utrecht, The Netherlands) for performing the 27-multiplex assay, the University Veterinary Diagnostic Laboratory (UVDL, University Utrecht, The Netherlands) for glucose and triglyceride measurements and Saskia Plomp for executing the surgeries. Funding Information: This research was funded by the Dutch Research Council (NWO), Domain Applied and Engineering Sciences (AES), Project Number: P15-23 project 2; and Translational Adult Stem Cell Research (TAS) Game changer grant from ZonMW (11600.420). The funding body had no role in study design, data collection, data analysis, data interpretation and writing the manuscript. Publisher Copyright: © 2023, The Author(s).
(Peer reviewed)