骨关节炎
医学
痹症科
SIRT6型
炎症
癌症研究
内科学
信号转导
炎症反应
巨噬细胞
内分泌学
免疫学
滑膜
炎性关节炎
关节炎
药理学
作者
Hao Wu,Weixue Sun,Qian Zhang,Gong Cheng,Zhilin Cao
标识
DOI:10.1186/s13075-025-03680-y
摘要
PURPOSE: This study aimed to evaluate the therapeutic effects of Omentin-1 on osteoarthritis and explore its protective mechanisms. METHODS: . After five weeks of Omentin-1 injection, we evaluated M1 and M2 macrophage distribution in the mouse synovium and measured inflammatory factor levels. Matrix proteins related to cartilage repair were detected, and safranin O-green and toluidine blue staining were used to evaluate the repair. Furthermore, we evaluated how Omentin-1 regulated macrophage polarization and explored potential mechanisms. RESULT: Omentin-1 was low in osteoarthritis mice and linked to M1 macrophage polarization. It protected these mice by reducing synovial inflammation, decreasing M1 macrophages, increasing M2 macrophages, and lowering pro-inflammatory factors while raising anti-inflammatory factors and minimizing inflammatory cell infiltration in the synovium. Omentin-1 enhanced Collagen II and α-SMA expression in cartilage, aiding repair. Further mechanistic studies indicated that Omentin-1 can enhance the expression of SIRT6 in the joint tissues of mice with osteoarthritis. Omentin-1's inhibition of inflammation in osteoarthritis mice was linked to SIRT6. CONCLUSION: Elevated Omentin-1 levels can mitigate the inflammatory response in osteoarthritis by enhancing SIRT6 expression, inhibiting inflammatory factors, suppressing M1 macrophages, and increasing M2 macrophages.
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