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Proteotoxic stress disrupts epithelial integrity by inducing MTOR sequestration and autophagy overactivation

Macroautophagy/autophagy, an evolutionarily conserved degradation system, serves to clear intracellular components through the lysosomal pathway. Mounting evidence has revealed cytoprotective roles of autophagy; however, the intracellular causes of overactivated autophagy, which has cytotoxic effect...

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Autores principales: Cheng, Xiaoxiang, Zhang, Pei, Zhao, Hongyu, Zheng, Hui, Zheng, Kai, Zhang, Hong, Zhang, Hongjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9809964/
https://www.ncbi.nlm.nih.gov/pubmed/35521960
http://dx.doi.org/10.1080/15548627.2022.2071381
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author Cheng, Xiaoxiang
Zhang, Pei
Zhao, Hongyu
Zheng, Hui
Zheng, Kai
Zhang, Hong
Zhang, Hongjie
author_facet Cheng, Xiaoxiang
Zhang, Pei
Zhao, Hongyu
Zheng, Hui
Zheng, Kai
Zhang, Hong
Zhang, Hongjie
author_sort Cheng, Xiaoxiang
collection PubMed
description Macroautophagy/autophagy, an evolutionarily conserved degradation system, serves to clear intracellular components through the lysosomal pathway. Mounting evidence has revealed cytoprotective roles of autophagy; however, the intracellular causes of overactivated autophagy, which has cytotoxic effects, remain elusive. Here we show that sustained proteotoxic stress induced by loss of the RING and Kelch repeat-containing protein C53A5.6/RIKE-1 induces sequestration of LET-363/MTOR complex and overactivation of autophagy, and consequently impairs epithelial integrity in C. elegans. In C53A5.6/RIKE-1-deficient animals, blocking autophagosome formation effectively prevents excessive endosomal degradation, mitigates mislocalization of intestinal membrane components and restores intestinal lumen morphology. However, autophagy inhibition does not affect LET-363/MTOR aggregation in animals with compromised C53A5.6/RIKE-1 function. Improving proteostasis capacity by reducing DAF-2 insulin/IGF1 signaling markedly relieves the aggregation of LET-363/MTOR and alleviates autophagy overactivation, which in turn reverses derailed endosomal trafficking and rescues epithelial morphogenesis defects in C53A5.6/RIKE-1-deficient animals. Hence, our studies reveal that C53A5.6/RIKE-1-mediated proteostasis is critical for maintaining the basal level of autophagy and epithelial integrity. Abbreviations: ACT-5: actin 5; ACTB: actin beta; ALs: autolysosomes; APs: autophagosomes; AJM-1: apical junction molecule; ATG: autophagy related; C. elegans: Caenorhabditis elegans; CPL-1: cathepsin L family; DAF: abnormal dauer formation; DLG-1: Drosophila discs large homolog; ERM-1: ezrin/radixin/moesin; EPG: ectopic P granule; GFP: freen fluorescent protein; HLH-30: helix loop helix; HSP: heat shock protein; LAAT-1: lysosome associated amino acid transporter; LET: lethal; LGG-1: LC3, GABARAP and GATE-16 family; LMP-1: LAMP (lysosome-associated membrane protein) homolog; MTOR: mechanistic target of rapamycin kinase; NUC-1: abnormal nuclease; PEPT-1/OPT-2: Peptide transporter family; PGP-1: P-glycoprotein related; RAB: RAB family; RIKE-1: RING and Kelch repeat-containing protein; SLCF-1: solute carrier family; SQST-1: sequestosome related; SPTL-1: serine palmitoyl transferase family.
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spelling pubmed-98099642023-01-04 Proteotoxic stress disrupts epithelial integrity by inducing MTOR sequestration and autophagy overactivation Cheng, Xiaoxiang Zhang, Pei Zhao, Hongyu Zheng, Hui Zheng, Kai Zhang, Hong Zhang, Hongjie Autophagy Research Paper Macroautophagy/autophagy, an evolutionarily conserved degradation system, serves to clear intracellular components through the lysosomal pathway. Mounting evidence has revealed cytoprotective roles of autophagy; however, the intracellular causes of overactivated autophagy, which has cytotoxic effects, remain elusive. Here we show that sustained proteotoxic stress induced by loss of the RING and Kelch repeat-containing protein C53A5.6/RIKE-1 induces sequestration of LET-363/MTOR complex and overactivation of autophagy, and consequently impairs epithelial integrity in C. elegans. In C53A5.6/RIKE-1-deficient animals, blocking autophagosome formation effectively prevents excessive endosomal degradation, mitigates mislocalization of intestinal membrane components and restores intestinal lumen morphology. However, autophagy inhibition does not affect LET-363/MTOR aggregation in animals with compromised C53A5.6/RIKE-1 function. Improving proteostasis capacity by reducing DAF-2 insulin/IGF1 signaling markedly relieves the aggregation of LET-363/MTOR and alleviates autophagy overactivation, which in turn reverses derailed endosomal trafficking and rescues epithelial morphogenesis defects in C53A5.6/RIKE-1-deficient animals. Hence, our studies reveal that C53A5.6/RIKE-1-mediated proteostasis is critical for maintaining the basal level of autophagy and epithelial integrity. Abbreviations: ACT-5: actin 5; ACTB: actin beta; ALs: autolysosomes; APs: autophagosomes; AJM-1: apical junction molecule; ATG: autophagy related; C. elegans: Caenorhabditis elegans; CPL-1: cathepsin L family; DAF: abnormal dauer formation; DLG-1: Drosophila discs large homolog; ERM-1: ezrin/radixin/moesin; EPG: ectopic P granule; GFP: freen fluorescent protein; HLH-30: helix loop helix; HSP: heat shock protein; LAAT-1: lysosome associated amino acid transporter; LET: lethal; LGG-1: LC3, GABARAP and GATE-16 family; LMP-1: LAMP (lysosome-associated membrane protein) homolog; MTOR: mechanistic target of rapamycin kinase; NUC-1: abnormal nuclease; PEPT-1/OPT-2: Peptide transporter family; PGP-1: P-glycoprotein related; RAB: RAB family; RIKE-1: RING and Kelch repeat-containing protein; SLCF-1: solute carrier family; SQST-1: sequestosome related; SPTL-1: serine palmitoyl transferase family. Taylor & Francis 2022-05-06 /pmc/articles/PMC9809964/ /pubmed/35521960 http://dx.doi.org/10.1080/15548627.2022.2071381 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Cheng, Xiaoxiang
Zhang, Pei
Zhao, Hongyu
Zheng, Hui
Zheng, Kai
Zhang, Hong
Zhang, Hongjie
Proteotoxic stress disrupts epithelial integrity by inducing MTOR sequestration and autophagy overactivation
title Proteotoxic stress disrupts epithelial integrity by inducing MTOR sequestration and autophagy overactivation
title_full Proteotoxic stress disrupts epithelial integrity by inducing MTOR sequestration and autophagy overactivation
title_fullStr Proteotoxic stress disrupts epithelial integrity by inducing MTOR sequestration and autophagy overactivation
title_full_unstemmed Proteotoxic stress disrupts epithelial integrity by inducing MTOR sequestration and autophagy overactivation
title_short Proteotoxic stress disrupts epithelial integrity by inducing MTOR sequestration and autophagy overactivation
title_sort proteotoxic stress disrupts epithelial integrity by inducing mtor sequestration and autophagy overactivation
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9809964/
https://www.ncbi.nlm.nih.gov/pubmed/35521960
http://dx.doi.org/10.1080/15548627.2022.2071381
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