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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

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 th...

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Autores principales: Chen, Huan-Da, Kao, Cheng-Yuan, Liu, Bang-Yu, Huang, Shin-Whei, Kuo, Cheng-Ju, Ruan, Jhen-Wei, Lin, Yen-Hung, Huang, Cheng-Rung, Chen, Yu-Hung, Wang, Horng-Dar, Aroian, Raffi V., Chen, Chang-Shi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324838/
https://www.ncbi.nlm.nih.gov/pubmed/27875098
http://dx.doi.org/10.1080/15548627.2016.1256933
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author Chen, Huan-Da
Kao, Cheng-Yuan
Liu, Bang-Yu
Huang, Shin-Whei
Kuo, Cheng-Ju
Ruan, Jhen-Wei
Lin, Yen-Hung
Huang, Cheng-Rung
Chen, Yu-Hung
Wang, Horng-Dar
Aroian, Raffi V.
Chen, Chang-Shi
author_facet Chen, Huan-Da
Kao, Cheng-Yuan
Liu, Bang-Yu
Huang, Shin-Whei
Kuo, Cheng-Ju
Ruan, Jhen-Wei
Lin, Yen-Hung
Huang, Cheng-Rung
Chen, Yu-Hung
Wang, Horng-Dar
Aroian, Raffi V.
Chen, Chang-Shi
author_sort Chen, Huan-Da
collection PubMed
description 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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spelling pubmed-53248382017-03-02 HLH-30/TFEB-mediated autophagy functions in a cell-autonomous manner for epithelium intrinsic cellular defense against bacterial pore-forming toxin in C. elegans Chen, Huan-Da Kao, Cheng-Yuan Liu, Bang-Yu Huang, Shin-Whei Kuo, Cheng-Ju Ruan, Jhen-Wei Lin, Yen-Hung Huang, Cheng-Rung Chen, Yu-Hung Wang, Horng-Dar Aroian, Raffi V. Chen, Chang-Shi Autophagy Basic Research Paper 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. Taylor & Francis 2016-11-22 /pmc/articles/PMC5324838/ /pubmed/27875098 http://dx.doi.org/10.1080/15548627.2016.1256933 Text en © 2017 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Basic Research Paper
Chen, Huan-Da
Kao, Cheng-Yuan
Liu, Bang-Yu
Huang, Shin-Whei
Kuo, Cheng-Ju
Ruan, Jhen-Wei
Lin, Yen-Hung
Huang, Cheng-Rung
Chen, Yu-Hung
Wang, Horng-Dar
Aroian, Raffi V.
Chen, Chang-Shi
HLH-30/TFEB-mediated autophagy functions in a cell-autonomous manner for epithelium intrinsic cellular defense against bacterial pore-forming toxin in C. elegans
title HLH-30/TFEB-mediated autophagy functions in a cell-autonomous manner for epithelium intrinsic cellular defense against bacterial pore-forming toxin in C. elegans
title_full HLH-30/TFEB-mediated autophagy functions in a cell-autonomous manner for epithelium intrinsic cellular defense against bacterial pore-forming toxin in C. elegans
title_fullStr HLH-30/TFEB-mediated autophagy functions in a cell-autonomous manner for epithelium intrinsic cellular defense against bacterial pore-forming toxin in C. elegans
title_full_unstemmed HLH-30/TFEB-mediated autophagy functions in a cell-autonomous manner for epithelium intrinsic cellular defense against bacterial pore-forming toxin in C. elegans
title_short HLH-30/TFEB-mediated autophagy functions in a cell-autonomous manner for epithelium intrinsic cellular defense against bacterial pore-forming toxin in C. elegans
title_sort hlh-30/tfeb-mediated autophagy functions in a cell-autonomous manner for epithelium intrinsic cellular defense against bacterial pore-forming toxin in c. elegans
topic Basic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324838/
https://www.ncbi.nlm.nih.gov/pubmed/27875098
http://dx.doi.org/10.1080/15548627.2016.1256933
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