Autophagic Degradation Is Involved in Cell Protection against Ricin Toxin

Toxins (Basel). 2023 Apr 23;15(5):304. doi: 10.3390/toxins15050304.

Abstract

Autophagy is a complex and highly regulated degradative process, which acts as a survival pathway in response to cellular stress, starvation and pathogen infection. Ricin toxin is a plant toxin produced by the castor bean and classified as a category B biothreat agent. Ricin toxin inhibits cellular protein synthesis by catalytically inactivating ribosomes, leading to cell death. Currently, there is no licensed treatment for patients exposed to ricin. Ricin-induced apoptosis has been extensively studied; however, whether its intoxication via protein synthesis inhibition affects autophagy is not yet resolved. In this work, we demonstrated that ricin intoxication is accompanied by its own autophagic degradation in mammalian cells. Autophagy deficiency, by knocking down ATG5, attenuates ricin degradation, thus aggravating ricin-induced cytotoxicity. Additionally, the autophagy inducer SMER28 (Small Molecule Enhancer 28) partially protects cells against ricin cytotoxicity, an effect not observed in autophagy-deficient cells. These results demonstrate that autophagic degradation acts as a survival response of cells against ricin intoxication. This suggests that stimulation of autophagic degradation may be a strategy to counteract ricin intoxication.

Keywords: ATG5; SMER28; autophagy; degradation; ricin toxin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Autophagy
  • Cytoprotection
  • Humans
  • Mammals / metabolism
  • Proteins
  • Ricin* / metabolism
  • Ricin* / toxicity

Substances

  • Ricin
  • Proteins

Grants and funding

This work was funded by the joint ministerial program of R&D against CBRNE risks, CEA and under Contracts ANR-18-CE18-0016 (LeishmaStop), ANR-20-CE18-0016 (SMERSEC) and ANR-20-SEBM-0001-01(PLANT). SIMoS and SCBM are members of the Laboratory of Excellence LERMIT, supported by a grant from the Agence Nationale de la Recherche (ANR-10-LABX-33). A.F. is a research associate of the FRS-FNRS.