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HLH-30/TFEB-mediated autophagy functions in a cell-autonomous manner for epithelium intrinsic cellular defense against bacterial pore-forming toxin in C-elegans

机译:HLH-30 / TFEB介导的自噬作用以细胞 - 自主方式用于上皮内皮细胞防御C-elegans中的细菌孔隙成形毒素

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摘要

Autophagy is an evolutionarily conserved intracellular system that maintains cellular homeostasis by degrading and recycling damaged cellular components. The transcription factor HLH-30/TFEB-mediated autophagy has been reported to regulate tolerance to bacterial infection, but less is known about the bona fide bacterial effector that activates HLH-30 and autophagy. Here, we reveal that bacterial membrane pore-forming toxin (PFT) induces autophagy in an HLH-30-dependent manner in Caenorhabditis elegans. Moreover, autophagy controls the susceptibility of animals to PFT toxicity through xenophagic degradation of PFT and repair of membrane-pore cell-autonomously in the PFT-targeted intestinal cells in C. elegans. These results demonstrate that autophagic pathways and autophagy are induced partly at the transcriptional level through HLH-30 activation and are required to protect metazoan upon PFT intoxication. Together, our data show a new and powerful connection between HLH-30-mediated autophagy and epithelium intrinsic cellular defense against the single most common mode of bacterial attack in vivo.
机译:自噬是一种进化保守的细胞内系统,通过降解和再循环受损的细胞组分来维持细胞稳态。据报道,转录因子HLH-30 / TFEB介导的自噬用于调节细菌感染的耐受,但是关于激活HLH-30和自噬的真菌细菌效应较少。在这里,我们揭示了细菌膜孔隙成形毒素(PFT)以HLH-30依赖性方式诱导自噬胶囊杆菌。此外,自噬通过通过在C.秀丽隐杆线虫的PFT靶向肠细胞中的姜黄和膜 - 孔细胞修复的仇外食管和修复,对动物对PFT毒性的易感性控制于PFT毒性。这些结果表明,通过HLH-30活化部分地在转录水平上诱导自噬途径和自噬,并且需要在PFT中毒时保护甲卓酮。在一起,我们的数据显示了HLH-30介导的自噬和上皮内皮内部细胞防御与体内单一最常见的细菌攻击模式之间的新的和强大的联系。

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