Cucurbitacin E inhibits TNF-α-induced inflammatory cytokine production in human synoviocyte MH7A cells via suppression of PI3K/Akt/NF-κB pathways

被引:74
作者
Jia, Qingyun [1 ,2 ,3 ]
Cheng, Wenxiang [1 ]
Yue, Ye [1 ]
Hu, Yipping [1 ]
Zhang, Jian [4 ]
Pan, Xiaohua [5 ]
Xu, Zhanwang [2 ]
Zhang, Peng [1 ,6 ]
机构
[1] Chinese Acad Sci, Shenzhen Inst Adv Technol, Translat Med R&D Ctr, Shenzhen 518055, Peoples R China
[2] Shandong Univ Tradit Chinese Med, Jinan 250355, Peoples R China
[3] Rizhao Hosp Tradit Chinese Med, Dept Orthoped, Rizhao 276800, Peoples R China
[4] Chinese Acad Sci, Shenzhen Inst Adv Technol, Lab Reprod Hlth, Shenzhen 518655, Peoples R China
[5] Shenzhen Baoan Peoples Hosp, Dept Orthoped, Shenzhen 518100, Peoples R China
[6] Shenzhen Bioact Mat Engn Lab Med, Shenzhen 518100, Peoples R China
基金
中国国家自然科学基金;
关键词
Cucurbitacin E; Rheumatoid arthritis; HP-kappa B; PI3K/Akt; Inflammation; MH7A; NF-KAPPA-B; RHEUMATOID-ARTHRITIS; ANTIINFLAMMATORY ACTIVITIES; CANCER CELLS; ACTIVATION; KINASE; CHEMOKINES; APOPTOSIS; DISEASE; BINDING;
D O I
10.1016/j.intimp.2015.08.026
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Increasing studies indicated that Cucurbitacin E (CuE), a compound isolated from Cucurbitaceae, has been shown anti-inflammatory effect. However, the effect of CuE on rheumatoid arthritis (RA) inflammatory response and its potential molecular mechanism are still unknown. In this study, we demonstrated that CuE significantly suppressed TNF-alpha-induced inflammatory cytokines production interleukin-1 beta (IL-1 beta), interleukin-6 (IL-6), and interleukin-8 (IL-8) mRNA and protein expression in human synoviocyte MH7A cells. Furthermore, we found that CuE also inhibited TNF-alpha-induced phosphorylation of NF-kappa Bp65, IKK alpha/beta, and I kappa B alpha in a dose-and time-dependent manner as well as NF-kappa Bp65 nuclear translocation. Finally, we showed that CuE blocked the upstream targets of NF-kappa B pathway RIP1/PI3K/Akt. Interestingly, PI3K inhibitor LY294002 completely blocked the TNF-alpha-induced activation of p85, Akt and the whole cascade of the NF-kappa B signaling components and suppressed inflammatory cytokines production in mRNA and protein levels similarly as CuE. Our studies provided the first evidence that CuE inhibited TNF-alpha-induced inflammatory cytokine production in human synoviocyte MH7A cells via modulation of PI3K/Akt/NF-kappa B pathway. These findings indicated that CuE is a potential candidate for RA therapy. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:884 / 890
页数:7
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