TY - JOUR
T1 - New mesenchymal stem/stromal cell-based strategies for osteoarthritis treatment
T2 - targeting macrophage-mediated inflammation to restore joint homeostasis
AU - Araya-Sapag, María Jesús
AU - Lara-Barba, Eliana
AU - García-Guerrero, Cynthia
AU - Herrera-Luna, Yeimi
AU - Flores-Elías, Yesenia
AU - Bustamante-Barrientos, Felipe A.
AU - Albornoz, Guillermo G.
AU - Contreras-Fuentes, Consuelo
AU - Yantén-Fuentes, Liliana
AU - Luque-Campos, Noymar
AU - Vega-Letter, Ana María
AU - Toledo, Jorge
AU - Luz-Crawford, Patricia
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2025.
PY - 2025
Y1 - 2025
N2 - Macrophages are pivotal in osteoarthritis (OA) pathogenesis, as their dysregulated polarization can contribute to chronic inflammatory processes. This review explores the molecular and metabolic mechanisms that influence macrophage polarization and identifies potential strategies for OA treatment. Currently, non-surgical treatments for OA focus only on symptom management, and their efficacy is limited; thus, mesenchymal stem/stromal cells (MSCs) have gained attention for their anti-inflammatory and immunomodulatory capabilities. Emerging evidence suggests that small extracellular vesicles (sEVs) derived from MSCs can modulate macrophage function, thus offering potential therapeutic benefits in OA. Additionally, the transfer of mitochondria from MSCs to macrophages has shown promise in enhancing mitochondrial functionality and steering macrophages toward an anti-inflammatory M2-like phenotype. While further research is needed to confirm these findings, MSC-based strategies, including the use of sEVs and mitochondrial transfer, hold great promise for the treatment of OA and other chronic inflammatory diseases.
AB - Macrophages are pivotal in osteoarthritis (OA) pathogenesis, as their dysregulated polarization can contribute to chronic inflammatory processes. This review explores the molecular and metabolic mechanisms that influence macrophage polarization and identifies potential strategies for OA treatment. Currently, non-surgical treatments for OA focus only on symptom management, and their efficacy is limited; thus, mesenchymal stem/stromal cells (MSCs) have gained attention for their anti-inflammatory and immunomodulatory capabilities. Emerging evidence suggests that small extracellular vesicles (sEVs) derived from MSCs can modulate macrophage function, thus offering potential therapeutic benefits in OA. Additionally, the transfer of mitochondria from MSCs to macrophages has shown promise in enhancing mitochondrial functionality and steering macrophages toward an anti-inflammatory M2-like phenotype. While further research is needed to confirm these findings, MSC-based strategies, including the use of sEVs and mitochondrial transfer, hold great promise for the treatment of OA and other chronic inflammatory diseases.
KW - Homeostasis
KW - Macrophages
KW - Osteoarthritis
UR - http://www.scopus.com/inward/record.url?scp=105003454461&partnerID=8YFLogxK
U2 - 10.1007/s00109-025-02547-8
DO - 10.1007/s00109-025-02547-8
M3 - Review article
AN - SCOPUS:105003454461
SN - 0946-2716
JO - Journal of Molecular Medicine
JF - Journal of Molecular Medicine
ER -