Yuqin Liu, Ming Nie, Xueyi Li, Hao Wang, Shaoju Ren, Dezheng Zou, Jianhui Liu, Ruidong Li
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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. 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引用次数: 0
摘要
骨关节炎(OA)是最常见的退行性关节疾病,影响着全球数百万人。大蒜衍生外泌体(GDEs)是从大蒜中提取的纳米颗粒,对其他疾病有抗炎作用,但GDEs对OA的作用尚未阐明。本研究提取并鉴定了 GDEs。软骨细胞经IL-1β处理后与GDEs体外培养,通过Western印迹法评估软骨基质成分(胶原蛋白II和凝集素)和基质降解酶(MMP3和MMP9)的表达。此外,还使用 Western 印迹法检测了 MAPK 通路的变化。使用高通量 RNA-seq 方法评估了与 GDE 干预相关的转录组变化。在体内,我们使用前交叉韧带切断术(ACLT)结合内侧半月板失稳(DMM)手术建立了小鼠 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了GDE的治疗效果。结果显示,IL-1β治疗抑制了胶原蛋白II和凝集素的表达,并上调了MMP3和MMP9的表达,而GDE的干预则减轻了这些影响。GDE 还能抑制 ERK、JNK 和 P38 的磷酸化。在体内,GDE 可减轻小鼠 OA 模型对热刺激的敏感性并改变行走步态。组织病理学分析表明,GDE干预可改善膝关节的关节破坏,且无明显毒性。研究结果证明,GDEs 在体外和体内都能缓解 OA 的进展,可能是一种潜在的 OA 疾病调节药物。
Garlic-derived Exosomes Alleviate Osteoarthritis Through Inhibiting the MAPK Signaling Pathway.
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.
期刊介绍:
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