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Terminalia Chebula provides protection against dual modes of necroptotic and apoptotic cell death upon death receptor ligation

机译:Terminalia Chebula提供了针对死亡受体结扎后坏死性和凋亡性细胞死亡的双重模式的保护

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Death receptor (DR) ligation elicits two different modes of cell death (necroptosis and apoptosis) depending on the cellular context. By screening a plant extract library from cells undergoing necroptosis or apoptosis, we identified a water extract of Terminalia chebula (WETC) as a novel and potent dual inhibitor of DR-mediated cell death. Investigation of the underlying mechanisms of its anti-necroptotic and anti-apoptotic action revealed that WETC or its constituents (e.g., gallic acid) protected against tumor necrosis factor-induced necroptosis via the suppression of TNF-induced ROS without affecting the upstream signaling events. Surprisingly, WETC also provided protection against DR-mediated apoptosis by inhibition of the caspase cascade. Furthermore, it activated the autophagy pathway via suppression of mTOR. Of the WETC constituents, punicalagin and geraniin appeared to possess the most potent anti-apoptotic and autophagy activation effect. Importantly, blockage of autophagy with pharmacological inhibitors or genetic silencing of Atg5 selectively abolished the anti-apoptotic function of WETC. These results suggest that WETC protects against dual modes of cell death upon DR ligation. Therefore, WETC might serve as a potential treatment for diseases characterized by aberrantly sensitized apoptotic or non-apoptotic signaling cascades.
机译:死亡受体(DR)的连接会根据细胞情况引发两种不同的细胞死亡模式(坏死和凋亡)。通过从经历坏死或凋亡的细胞中筛选植物提取物文库,我们确定了Terminalia chebula(WETC)的水提取物是DR介导的细胞死亡的新型有效双重抑制剂。对它的抗坏死性和抗凋亡作用的潜在机制的研究表明,WETC或其成分(例如没食子酸)通过抑制TNF引起的ROS而保护了肿瘤坏死因子引起的坏死性细胞,而不影响上游信号转导事件。出人意料的是,WETC还通过抑制caspase级联反应,提供了针对DR介导的细胞凋亡的保护作用。此外,它通过抑制mTOR激活了自噬途径。在WETC成分中,punicalagin和geraniin似乎具有最有效的抗凋亡和自噬激活作用。重要的是,用药理学抑制剂阻止自噬或Atg5的基因沉默选择性地废除了WETC的抗凋亡功能。这些结果表明,WETC可防止DR结扎后细胞死亡的双重模式。因此,WETC可以作为以异常敏化的凋亡或非凋亡信号转导级联为特征的疾病的潜在治疗方法。

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