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依利替康阻断白介素-17A 和肿瘤坏死因子-α 在细胞上皮中的协同作用,并缓解急性胰腺炎相关急性肺损伤。

Ellipticine blocks synergistic effects of IL-17A and TNF-α in epithelial cells and alleviates severe acute pancreatitis-associated acute lung injury.

机构信息

Engineering Research Center of Cell & Therapeutic Antibody, Ministry of Education, School of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, PR China.

Engineering Research Center of Cell & Therapeutic Antibody, Ministry of Education, School of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, PR China; Anhui Province Key Laboratory of Translational Cancer Research, Bengbu Medical College, Bengbu, Anhui Province 233003, PR China.

出版信息

Biochem Pharmacol. 2020 Jul;177:113992. doi: 10.1016/j.bcp.2020.113992. Epub 2020 Apr 23.

DOI:10.1016/j.bcp.2020.113992
PMID:32335141
Abstract

IL-17A combined with TNF-α plays a vital role in inflammatory response and interference of the synergistic effect is an effective strategy for treating inflammatory diseases. Ellipticine, a natural alkaloid, has biological activities on anti-tumor and anti-HIV. However, it is still unknown whether ellipticine can inhibit IL-17A and TNF-α-mediated signaling and has treatment effect on PALI. Here, we reported that ellipticine significantly inhibited the production of pro-inflammatory cytokines and chemokines in pulmonary epithelial cell BEAS-2B treated with IL-17A and TNF-α, but not IL-17A or TNF-α alone. Meanwhile, ellipticine attenuated NF-κB and MAPKs activation in response to IL-17A and TNF-α treatment, inhibited Act1 and TRAF6-mediated NF-κB activation, and blocked the interaction of Act1 with TRAF6. Furthermore, we found that ellipticine significantly alleviated CAE and LPS-induced SAP/PALI. Ellipticine treatment dramatically reduced inflammatory cells infiltration, MPO activity, serum amylase and lipase activity and the protein concentration of BALF. Collectively, our findings indicate that ellipticine inhibits the synergistic effect of IL-17A and TNF-α by targeting on Act1 and TRAF6 interaction and is a potential therapeutic agent for the treatment of SAP/PALI.

摘要

IL-17A 与 TNF-α 共同发挥重要作用,干扰协同效应是治疗炎症性疾病的有效策略。依替膦酸,一种天然生物碱,具有抗肿瘤和抗 HIV 的生物活性。然而,目前尚不清楚依替膦酸是否可以抑制 IL-17A 和 TNF-α 介导的信号转导,以及对 PALI 是否具有治疗作用。在这里,我们报道了依替膦酸可显著抑制 IL-17A 和 TNF-α 处理的肺上皮细胞 BEAS-2B 中促炎细胞因子和趋化因子的产生,但对单独的 IL-17A 或 TNF-α 没有作用。同时,依替膦酸减弱了 NF-κB 和 MAPKs 对 IL-17A 和 TNF-α 处理的激活,抑制了 Act1 和 TRAF6 介导的 NF-κB 激活,并阻断了 Act1 与 TRAF6 的相互作用。此外,我们发现依替膦酸可显著减轻 CAE 和 LPS 诱导的 SAP/PALI。依替膦酸治疗可显著减少炎症细胞浸润、MPO 活性、血清淀粉酶和脂肪酶活性以及 BALF 中的蛋白浓度。综上所述,我们的研究结果表明,依替膦酸通过靶向 Act1 和 TRAF6 相互作用抑制 IL-17A 和 TNF-α 的协同效应,是治疗 SAP/PALI 的潜在治疗剂。

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