Nuclear translocation of endonuclease G and apoptosis-inducing factor during acetaminophen-induced liver cell injury

Toxicol Sci. 2006 Nov;94(1):217-25. doi: 10.1093/toxsci/kfl077. Epub 2006 Aug 8.

Abstract

Mitochondrial dysfunction and internucleosomal DNA fragmentation are well-recognized features of acetaminophen (AAP)-induced hepatocyte cell death. However, the endonucleases responsible for this effect have not been identified. Apoptosis-inducing factor (AIF) and endonuclease G are nucleases located in the intermembrane space of mitochondria. AIF is thought to trigger chromatin condensation and induce cleavage of DNA into high molecular weight fragments (50-300 kb), and endonuclease G can produce oligonucleosomal DNA fragments. Therefore, the objective of this investigation was to test the hypothesis that endonuclease G and AIF could be involved in AAP-induced nuclear DNA fragmentation. Using immunofluorescence microscopy, it was shown that in primary cultured mouse hepatocytes, endonuclease G and AIF translocated to the nucleus between 3 and 6 h after exposure to 5 mM AAP. In contrast, other mitochondrial intermembrane proteins such as cytochrome c or the second mitochondria-derived activator of caspases (Smac) did not accumulate in the nucleus. The translocation of AIF and endonuclease G correlated with mitochondrial dysfunction as indicated by the progressive loss of the mitochondrial membrane potential (measured with the JC-1 assay) and the appearance of nuclear DNA fragments in the cytosol (determined by an anti-histone ELISA). Pretreatment with 20mM N-acetylcysteine prevented mitochondrial dysfunction, the nuclear translocation of endonuclease G and AIF, and the nuclear DNA fragmentation. The data support the conclusion that endonuclease G and AIF translocate to the nucleus in response to AAP-induced mitochondrial dysfunction and may be responsible, at least in part, for the initial DNA fragmentation during AAP hepatotoxicity.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acetaminophen / toxicity*
  • Acetylcysteine / pharmacology
  • Active Transport, Cell Nucleus
  • Animals
  • Apoptosis Inducing Factor / metabolism*
  • Apoptosis Regulatory Proteins
  • Benzimidazoles / metabolism
  • Carbocyanines / metabolism
  • Carrier Proteins / metabolism
  • Cell Nucleus / drug effects*
  • Cell Nucleus / metabolism
  • Cell Survival / drug effects
  • Cells, Cultured
  • Cytochromes c / metabolism
  • DNA Fragmentation / drug effects
  • Endodeoxyribonucleases / metabolism*
  • Hepatocytes / cytology
  • Hepatocytes / drug effects*
  • Hepatocytes / metabolism
  • Immunohistochemistry / methods
  • Male
  • Membrane Potential, Mitochondrial / drug effects
  • Mice
  • Mice, Inbred C3H
  • Microscopy, Fluorescence / methods
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Mitochondria / physiology
  • Mitochondrial Proteins / metabolism

Substances

  • Apoptosis Inducing Factor
  • Apoptosis Regulatory Proteins
  • Benzimidazoles
  • Carbocyanines
  • Carrier Proteins
  • Diablo protein, mouse
  • Mitochondrial Proteins
  • 5,5',6,6'-tetrachloro-1,1',3,3'-tetraethylbenzimidazolocarbocyanine
  • Acetaminophen
  • Cytochromes c
  • Endodeoxyribonucleases
  • endonuclease G
  • Acetylcysteine