Development and characterization of a humanized mouse model of osteoarthritis. Issue 6 (June 2022)

• Record Type: Journal Article
• Authors: Bodic, B.; Boutet, M.A.; Boyer, C.; Metayer, B.; Vignes, C.; Lesoeur, J.; Veziers, J.; Daguin, V.; Haspot, F.; Maugars, Y.; Djouad, F.; Guicheux, J.; Vinatier, C.
• Is Part Of: Osteoarthritis and cartilage. Volume 30:Issue 6(2022)
• Page Start: 875
• Page End: 885
• Publication Date: 2022-06
• Subjects: Osteoarthritis -- Animal model -- Humanized mouse -- DMM; Osteoarthritis -- Periodicals; Cartilage -- Periodicals; Osteoarthritis -- Periodicals; Cartilage -- Periodicals; Arthrose -- Périodiques; Articulations -- Maladies -- Périodiques; 616.7223005
• DOI: 10.1016/j.joca.2022.02.620
• Languages: English
• ISSNs: 1063-4584

Abstract

Summary: Objective: In light of the role of immune cells in OA pathogenesis, the development of sophisticated animal models closely mimicking the immune dysregulation during the disease development and progression could be instrumental for the preclinical evaluation of novel treatments. Among these models, immunologically humanized mice may represent a relevant system, particularly for testing immune-interacting DMOADs or cell therapies before their transfer to the clinic. Our objective, therefore, was to develop an experimental model of OA by destabilization of the medial meniscus (DMM) in humanized mice. Method: Irradiated 5-week-old NOD/LtSz-scid IL2Rγ null (NSG) mice were humanized by intravenous injection of CD34 + human hematopoietic stem cells. The engraftment efficiency was evaluated by flow cytometry 17 weeks after the humanization procedure. Humanized and non-humanized NSG mice underwent DMM or sham surgery and OA development was assessed 1, 6, and 12 weeks after the surgery. Results: 120 days after the humanization, human T and B lymphocytes, macrophages and NK cells, were present in the blood and spleen of the humanized NSG mice. The DMM surgery induced articular cartilage and meniscal alterations associated with an increase in OA and the meniscal score. Moreover, the surgery triggered an inflammatory response that was sustained at a low grade in the DMM group. Conclusions: Our study shows for the first time the feasibility of inducing OA by DMM in humanized mice. This novel OA model could constitute a useful tool to bridge the gap between the preclinical and clinical evaluation of immune interacting DMOADs and cell-based therapies.