Liu Yuqin, Nie Ming, Li Xueyi, Wang Hao, Ren Shaoju, Zou Dezheng, Liu Jianhui, Li Ruidong
College of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing, 400054, China.
Center for Joint Surgery, Department of Orthopedic Surgery, the Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, China.
Appl Biochem Biotechnol. 2025 Jan;197(1):518-533. doi: 10.1007/s12010-024-05047-6. Epub 2024 Aug 27.
Osteoarthritis (OA) is the most common degenerative joint disease affecting millions of people worldwide. Garlic-derived exosomes (GDEs) are nanoparticles extracted from garlic that exhibit anti-inflammatory effects on other diseases, but the effect of GDEs on OA has not been elucidated. In this study, GDEs were extracted and characterized. Chondrocytes were treated with IL-1β and incubated with GDEs in vitro, and the expression of cartilage matrix components (collagen II and aggrecan) and matrix degrading enzymes (MMP3 and MMP9) was evaluated via Western blotting. Changes in the MAPK pathway was also examined using Western blotting. The transcriptomic changes associated with GDE intervention were evaluated using high-throughput RNA-seq method. In vivo, we used anterior cruciate ligament transection (ACLT) combined with destabilization of the medial meniscus (DMM) surgery to establish a mouse OA model, and GDEs was intraarticularly injected into the joint cavity. The therapeutic effect of GDE was evaluated by behavioral and histopathological analysis. The results showed that IL-1β treatment inhibited the expression of collagen II and aggrecan, and upregulated the expression of MMP3 and MMP9, while GDE intervention alleviated these effects. GDEs also inhibited the phosphorylation of ERK, JNK, and P38. In vivo, GDE alleviated the sensitivity to heat stimulation and altered walking gait in a mouse OA model. Histopathological analysis indicated that GDE intervention ameliorated joint destruction in the knee joint without obvious toxicity. The results proved that GDEs alleviated the progression of OA in vitro and in vivo, and may be a potential disease-modifying drug for OA.
骨关节炎(OA)是影响全球数百万人的最常见的退行性关节疾病。大蒜衍生的外泌体(GDEs)是从大蒜中提取的纳米颗粒,对其他疾病具有抗炎作用,但GDEs对OA的作用尚未阐明。在本研究中,提取并表征了GDEs。用IL-1β处理软骨细胞,并在体外与GDEs孵育,通过蛋白质印迹法评估软骨基质成分(胶原蛋白II和聚集蛋白聚糖)和基质降解酶(MMP3和MMP9)的表达。还使用蛋白质印迹法检测了MAPK途径的变化。使用高通量RNA测序方法评估与GDE干预相关的转录组变化。在体内,我们使用前交叉韧带横断术(ACLT)联合内侧半月板不稳定(DMM)手术建立小鼠OA模型,并将GDEs关节腔内注射。通过行为学和组织病理学分析评估GDE的治疗效果。结果表明,IL-1β处理抑制了胶原蛋白II和聚集蛋白聚糖的表达,并上调了MMP3和MMP9的表达,而GDE干预减轻了这些作用。GDEs还抑制了ERK、JNK和P38的磷酸化。在体内,GDE减轻了小鼠OA模型对热刺激的敏感性并改变了行走步态。组织病理学分析表明,GDE干预改善了膝关节的关节破坏,且无明显毒性。结果证明,GDEs在体外和体内均减轻了OA的进展,可能是一种潜在的OA病情改善药物。