Li Yu, Ouyang Yu, Lang Ruibo, He Jing, Zheng Shuo, Ao Chunchun, Jiang Yijia, Xiao Huan, Li Mao, Li Changyong, Wu Dongcheng
R&D Center, Wuhan Hamilton Biotechnology Co. Ltd, Wuhan, Hubei, China.
School of Public Health, Hubei University of Medicine, Shiyan, Hubei, China.
Stem Cells Int. 2025 Aug 30;2025:7558817. doi: 10.1155/sci/7558817. eCollection 2025.
Osteoarthritis (OA) is the leading joint disease that causes joint pain and disability. Despite increasing progress regarding the therapeutic potential of human umbilical cord mesenchymal stem cells (UC-MSCs) for OA, effective strategies for the treatment of OA using UC-MSCs have not yet been developed in clinical practice. Our present study has proven that the early stage in OA rats is the main development stage of nod-like receptor heat protein domain protein 3 (NLRP3)-mediated synovial inflammation. The middle stage in OA rats is the main development stage of chondrocyte apoptosis. The late stage in OA rats is the main development stage of synovial fibrosis. The treatment of UC-MSCs in the early and middle stages of OA significantly reduced cartilage damage in rats, and improved the pathological structure of the knee joint. In comparison, UC-MSCs effectively reduced chondrocyte apoptosis in the early and middle stages of OA rats, but they only effectively reduced NLRP3-mediated synovial inflammation in the early stages of OA rats. Experiments in vitro showed that UC-MSCs could inhibit NLRP3-mediated pyroptosis of rat primary synovial cells (Rat-scs). In conclusion, our findings suggest that UC-MSCs exert therapeutic effects on OA, at least in part, through inhibiting NLRP3-mediated synovial inflammation in the early stage of OA.
骨关节炎(OA)是导致关节疼痛和残疾的主要关节疾病。尽管人类脐带间充质干细胞(UC-MSCs)治疗OA的潜在疗效取得了越来越多的进展,但在临床实践中尚未开发出使用UC-MSCs治疗OA的有效策略。我们目前的研究证明,OA大鼠的早期是核苷酸结合寡聚化结构域样受体热蛋白结构域相关蛋白3(NLRP3)介导的滑膜炎症的主要发展阶段。OA大鼠的中期是软骨细胞凋亡的主要发展阶段。OA大鼠的晚期是滑膜纤维化的主要发展阶段。在OA的早期和中期用UC-MSCs治疗可显著减少大鼠的软骨损伤,并改善膝关节的病理结构。相比之下,UC-MSCs在OA大鼠的早期和中期有效减少软骨细胞凋亡,但仅在OA大鼠的早期有效减少NLRP3介导的滑膜炎症。体外实验表明,UC-MSCs可抑制大鼠原代滑膜细胞(Rat-scs)的NLRP3介导的焦亡。总之,我们的研究结果表明,UC-MSCs至少部分地通过抑制OA早期NLRP3介导的滑膜炎症对OA发挥治疗作用。