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Updated: Sep 24, 2025

Cecal Ligation and Puncture-induced Sepsis as a Model To Study Autophagy in Mice
Published on: February 9, 2014
Proteotoxic stress disrupts epithelial integrity by inducing MTOR sequestration and autophagy overactivation
Xiaoxiang Cheng1,2, Pei Zhang1, Hongyu Zhao2
1Centre of Reproduction, Development and Aging, Faculty of Health Sciences, University of Macau, Taipa, Macau, China.
Abstract:
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.
Insights
Loss of RIKE-1 protein causes proteotoxic stress, leading to overactivated autophagy and impaired epithelial integrity in C. elegans. Restoring proteostasis rescues these defects, highlighting RIKE-1
Area of Science:
- Cell Biology
- Molecular Biology
- Genetics
Background:
- Autophagy is a conserved degradation system crucial for cellular homeostasis.
- While generally cytoprotective, overactivated autophagy can be cytotoxic, but its causes are not fully understood.
- Epithelial integrity is vital for organismal function and can be compromised by cellular stress.
Purpose of the Study:
- To investigate the intracellular causes of cytotoxic overactivated autophagy.
- To elucidate the role of the RING and Kelch repeat-containing protein C53A5.6/RIKE-1 in regulating autophagy and epithelial integrity.
- To identify mechanisms by which proteotoxic stress impacts autophagy and cellular function.
Main Methods:
- Utilized Caenorhabditis elegans as a model organism.
- Investigated the effects of C53A5.6/RIKE-1 deficiency on autophagy, proteostasis, and epithelial morphology.
- Employed genetic manipulation to block autophagosome formation and modulate insulin/IGF-1 signaling.
- Analyzed LET-363/MTOR complex sequestration and endosomal trafficking.
Main Results:
- Loss of C53A5.6/RIKE-1 induces sustained proteotoxic stress, leading to LET-363/MTOR complex aggregation and autophagy overactivation.
- This overactivation impairs epithelial integrity by disrupting endosomal trafficking and intestinal morphology.
- Inhibition of autophagy ameliorates defects caused by C53A5.6/RIKE-1 loss, but does not affect LET-363/MTOR aggregation.
- Enhancing proteostasis via reduced DAF-2 insulin/IGF1 signaling alleviates LET-363/MTOR aggregation and rescues epithelial defects.
Conclusions:
- C53A5.6/RIKE-1-mediated proteostasis is essential for maintaining basal autophagy levels.
- Dysregulation of proteostasis can lead to cytotoxic autophagy and compromised epithelial integrity.
- Targeting proteostasis pathways offers a potential strategy to manage autophagy-related cellular damage.
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