坏死性下垂
布雷菲尔德A
化学
肿瘤坏死因子α
细胞凋亡
磷酸化
细胞生物学
程序性细胞死亡
真菌
生物化学
植物
生物
高尔基体
免疫学
细胞
作者
Jiayi Shi,Chao‐Feng Wang,Ming‐Min Xie,You‐Jia Hao,Ning Wang,Hua‐Bin Ma,Xian‐Wen Yang
标识
DOI:10.1002/cbdv.202200696
摘要
From the deep-sea-derived Fusarium sp. ZEN-48, four known compounds were obtained. Their structures were established by extensive analyses of the NMR, HR-ESI-MS, and the X-ray crystallographic data as brefeldin A (BFA, 1), brevianamide F (2), N-acetyltryptamine (3), and (+)-diaporthin (4). Although BFA was extensively investigated for its potent bioactivities, its role on TNFα-induced necroptosis was incompletely understood. In this study, BFA showed significant inhibition on TNFα-induced necroptosis by disrupting the necrosome formation and suppressing the phosphorylation of RIPK3 and MLKL (IC50 =0.5 μM). While, it had no effect on TNFα-induced NF-κB/MAPKs activation and apoptosis. The finding raised significant implications of BFA for necroptosis-related inflammatory disease therapy and new drug development from marine fungi.
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