骨关节炎
巨噬细胞极化
医学
细胞因子
巨噬细胞
脂肪因子
安普克
软骨
PI3K/AKT/mTOR通路
炎症
体内
促炎细胞因子
内科学
免疫学
癌症研究
内分泌学
信号转导
瘦素
病理
生物
细胞生物学
磷酸化
体外
肥胖
解剖
替代医学
生物技术
蛋白激酶A
生物化学
作者
Chih‐Yuan Ko,Yen‐You Lin,David Achudhan,Jun‐Way Chang,Shan‐Chi Liu,Chao-Yang Lai,Yuan‐Li Huang,Chun‐Hao Tsai,Yi‐Chin Fong,Hsien-Te Chen,Kun‐Tsan Lee,Chien‐Chung Huang,Ting‐Kuo Chang,Chih‐Hsin Tang
摘要
Osteoarthritis (OA) is a prevalent joint disease commonly associated with aging and obesity, which can lead to pain, stiffness, joint dysfunction, and disability. Omentin-1 (also called intelectin-1) is a newly discovered adipokine, which plays a protective role in suppressing the secretion of pro-inflammatory cytokines. Based on data from the Gene Expression Omnibus (GEO) dataset and clinical samples obtained at our institution revealed, determined that omentin-1 and IL-4 (an anti-inflammatory cytokine) levels were significantly lower in OA patients than in normal controls. Omentin-1 was shown to induce IL-4-depedent anti-inflammatory responses and M2 macrophage polarization in OA synovial fibroblasts via the PI3K, ERK, and AMPK pathways. Administering omentin-1 was shown to block cartilage degradation and bone erosion resulting from anterior cruciate ligament transection by inhibiting the production of pro-inflammatory cytokines and promoting M2 macrophage polarization in vivo. Our findings indicate omentin-1 as a promising therapeutic avenue for the treatment for OA.
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