Aflatoxin B1 induces ROS-dependent mitophagy by modulating the PINK1/Parkin pathway in HepG2 cells

Basic Clin Pharmacol Toxicol. 2024 Aug;135(2):195-209. doi: 10.1111/bcpt.14034. Epub 2024 May 28.

Abstract

Aflatoxin B1 (AFB1) is extremely harmful to both humans and animals. Mitophagy is a selective process of self-elimination and has an important role in controlling mitochondrial quality. The present study aimed to investigate the effect of reactive oxygen species (ROS) accumulation on AFB1-induced mitophagy in HepG2 cells to provide a new perspective from which to design novel therapeutic strategies to treat AFB1 poisoning. ROS release was induced in HepG2 cells with AFB1 (10 μmol/L). Cell autophagy activity, mitochondrial membrane potential (MMP), adenosine triphosphate (ATP) levels, Parkin translocation and both the transcription and expression of mitophagy-related proteins were measured when N-acetyl-L-cysteine (NAC) partially decreased the ROS level, while the knockdown of nuclear factor erythroid 2-related factor 2 (Nrf2) resulted in a large accumulation of ROS. The results reveal that NAC pretreatment ameliorated the decline in both the MMP and the ATP levels while also activating phosphoglycerate mutase 5 (PGAM5)-PTEN-induced kinase 1 (PINK1)/Parkin, while the Nrf2 knockdown group exhibited the opposite trend. These results suggest that AFB1-induced mitophagy in HepG2 cells depends on ROS, and proper ROS activates mitophagy to play a protective role.

Keywords: Nrf2; PINK1/Parkin; aflatoxins B1; mitophagy; reactive oxygen species.

MeSH terms

  • Acetylcysteine / pharmacology
  • Adenosine Triphosphate* / metabolism
  • Aflatoxin B1* / toxicity
  • Hep G2 Cells
  • Humans
  • Membrane Potential, Mitochondrial* / drug effects
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism
  • Mitophagy* / drug effects
  • NF-E2-Related Factor 2* / genetics
  • NF-E2-Related Factor 2* / metabolism
  • Phosphoprotein Phosphatases / genetics
  • Phosphoprotein Phosphatases / metabolism
  • Protein Kinases* / metabolism
  • Reactive Oxygen Species* / metabolism
  • Signal Transduction / drug effects
  • Ubiquitin-Protein Ligases* / genetics
  • Ubiquitin-Protein Ligases* / metabolism

Substances

  • parkin protein
  • Reactive Oxygen Species
  • Ubiquitin-Protein Ligases
  • PTEN-induced putative kinase
  • Protein Kinases
  • Aflatoxin B1
  • Adenosine Triphosphate
  • NF-E2-Related Factor 2
  • NFE2L2 protein, human
  • PGAM5 protein, human
  • Phosphoprotein Phosphatases
  • Acetylcysteine
  • Mitochondrial Proteins