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.

Autophagy
|May 6, 2022
PubMed

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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