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

نویسندگان

  • Huan-Da Chen
  • Cheng-Yuan Kao
  • Bang-Yu Liu
  • Shin-Whei Huang
  • Cheng-Ju Kuo
  • Jhen-Wei Ruan
  • Yen-Hung Lin
  • Cheng-Rung Huang
  • Yu-Hung Chen
  • Horng-Dar Wang
  • Raffi V. Aroian
  • Chang-Shi Chen
چکیده

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.

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عنوان ژورنال:

دوره 13  شماره 

صفحات  -

تاریخ انتشار 2017