ACY-1215 exhibits anti-inflammatory and chondroprotective effects in human osteoarthritis chondrocytes via inhibition of STAT3 and NF-κB signaling pathways

被引:43
作者
Cheng, Chao [1 ]
Shan, Wenshan [2 ]
Huang, Wei [2 ,4 ]
Ding, Zhenfei [2 ]
Cui, Guanjun [2 ]
Liu, Fuen [2 ]
Lu, Wei [2 ]
Xu, Jiegou [3 ]
He, Wei [3 ]
Yin, Zongsheng [1 ]
机构
[1] Anhui Med Univ, Affiliated Hosp 4, Dept Orthopaed, 372 Tun Xi Rd, Hefei 230032, Anhui, Peoples R China
[2] Anhui Med Univ, Affiliated Hosp 1, Dept Orthopaed, 218 Ji Xi Rd, Hefei 230032, Anhui, Peoples R China
[3] Anhui Med Univ, Sch Basic Med Sci, 81 Mei Shan Rd, Hefei 230032, Anhui, Peoples R China
[4] Univ Sci & Technol China, Affiliated Hosp USTC 1, Div Life Sci & Med, Dept Orthopaed, 17 Lu Jiang Rd, Hefei 230001, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Osteoarthritis; ACY-1215; HDAC6; STAT3; NF-kappa B; Chondrocytes; SELECTIVE COX-2 INHIBITION; GENE-EXPRESSION; PROSTAGLANDIN E-2; II COLLAGEN; IN-VITRO; CARTILAGE; INTERLEUKIN-1-BETA; DEGRADATION; ACTIVATION; ARTHRITIS;
D O I
10.1016/j.biopha.2018.11.017
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Cartilage degeneration is a basic pathological feature of osteoarthritis (OA), and there is growing evidence that it is associated with inflammation. ACY-1215, a selective HDAC6 inhibitor, has been reported to have anti-inflammatory effects. Here, we investigated the anti-inflammatory and chondroprotective effects of ACY-1215 in IL-1 beta-stimulated human primary chondrocytes and C28/I2 cells. The results suggested that ACY-1215 can markedly suppress the expression of inflammatory factors, including IL-1 beta and IL-6 in human primary chondrocytes and C28/I2 cells. Furthermore, ACY-1215 exerts potent chondroprotection through the amelioration of cartilage degradation by inhibiting the expression of matrix-degrading proteases, including MMP-1 and MMP-13 in chondrocytes. These effects may be related to ACY-1215 induced down-regulation of NF-kappa B and STAT3 pathways in OA chondrocytes. Taken together, our results show that ACY-1215 may be a potential and promising therapeutic drug for the management of OA.
引用
收藏
页码:2464 / 2471
页数:8
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