4.8 Article

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

Journal

AUTOPHAGY
Volume 13, Issue 2, Pages 371-385

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/15548627.2016.1256933

Keywords

autophagy; C. elegans; effector triggered immunity (ETI); HLH-30; TFEB; intrinsic cellular defense (INCED); pore-forming toxin (PFT); surveillance immunity

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Funding

  1. NIH [R01GM071603]
  2. Ministry of Science and Technology, Taiwan [MOST 97-2311-B-006-007, 98-2311-B-006-002-MY3, 103-2311-B-006-005-MY3]

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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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