BMSCs-derived Mitochondria Improve Osteoarthritis by Ameliorating Mitochondrial Dysfunction and Promoting Mitochondrial Biogenesis in Chondrocytes

被引:31
作者
Yu, Mingchuan [1 ]
Wang, Di [1 ]
Chen, Xiang [1 ]
Zhong, Da [1 ]
Luo, Jun [1 ]
机构
[1] Nanchang Univ, Dept Rehabil Med, Affiliated Hosp 2, 1 Minde Rd, Nanchang 330006, Jiangxi, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Osteoarthritis; Mitochondrial dysfunction; Microvesicle; Mitochondrial transplantation; Mitochondrial biogenesis; TRANSPLANTATION; PROGRESSION; EXOSOMES;
D O I
10.1007/s12015-022-10436-7
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Bone marrow mesenchymal stem cells (BMSCs)-derived exosomes and microvesicles can effectively improve knee osteoarthritis. We found that microvesicles performed a superior effect on improving mitochondrial function in chondrocytes than exosomes, which may be related to the ability of microvesicles carrying active mitochondria to replace damaged ones in chondrocytes. This study investigated the therapeutic effect of direct mitochondrial transplantation (MT) on knee osteoarthritis. IL-1 beta stimulated the osteoarthritis phenotype of rat chondrocytes, and the effect of BMSCs-derived mitochondria transplantation was observed in vitro. Knee osteoarthritis rat model was established by collagenase induction to observe the effect of intra-articular injection of mitochondria. Results showed that the mitochondria of BMSCs could be ingested by rat chondrocytes via co-incubation in vitro, and significantly improved osteoarthritis phenotype and mitochondrial function, and inhibited chondrocytes apoptosis. In vivo, BMSCs-derived mitochondria could be ingested by cartilage via intra-articular injection, ameliorated pathological cartilage injury, suppressed inflammation, inhibited chondrocytes apoptosis, and improved osteoarthritis phenotype. In addition, MT promoted mitochondrial biogenesis in chondrocytes by activating PGC-1 alpha signaling. All above results suggest that BMSCs-derived mitochondria transplantation ameliorates knee osteoarthritis by improving chondrocytes mitochondrial dysfunction and promoting mitochondrial biogenesis.
引用
收藏
页码:3092 / 3111
页数:20
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