Mitochondrial oxygen consumption inhibition importance for TMT-dependent cell death in undifferentiated PC12 cells

Neurochem Int. 2008 May;52(6):1092-9. doi: 10.1016/j.neuint.2007.11.008. Epub 2007 Dec 4.

Abstract

The evolving role of mitochondria as a target for different death-inducing noxae prompted us to investigate trimethyltin (TMT)-dependent effects on mitochondrial functionality. For this purpose, we used a homogeneous cell culture model represented by undifferentiated PC12 cells. Mitochondria isolated from PC12 cells treated with TMT for 6, 12 and 24h, showed a time-dependent inhibition of ADP-stimulated oxygen consumption using succinate or glutamate/malate as substrate. Using a fluorescent assay, the effect of TMT on mitochondrial membrane potential (delta Psi) in PC12 cells was also determined. After 24h in culture, a strong loss of mitochondrial membrane potential (delta Psi) was observed in TMT-treated cells. Collapse of mitochondrial membrane potential correlated with an increased expression of bax/bcl-2 ratio, as evaluated by polymerase chain reaction. Western blotting and spectrophotometric analysis showed that cytochrome c release and activation of caspase 3 were concurrently induced. Our findings suggest that inhibition of mitochondrial respiration represents the early toxic event for cell death in PC12 due to trimethyltin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Apoptosis / physiology
  • Caspase 3 / drug effects
  • Caspase 3 / metabolism
  • Cell Respiration / drug effects
  • Cell Respiration / physiology
  • Cytochromes c / drug effects
  • Cytochromes c / metabolism
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / physiology
  • Membrane Potential, Mitochondrial / drug effects
  • Membrane Potential, Mitochondrial / physiology
  • Mitochondria / drug effects*
  • Mitochondria / metabolism
  • Nerve Degeneration / chemically induced*
  • Nerve Degeneration / metabolism
  • Nerve Degeneration / physiopathology
  • Neurotoxins / toxicity
  • Oxygen Consumption / drug effects*
  • Oxygen Consumption / physiology
  • PC12 Cells
  • Proto-Oncogene Proteins c-bcl-2 / drug effects
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Rats
  • Trimethyltin Compounds / toxicity*
  • bcl-2-Associated X Protein / drug effects
  • bcl-2-Associated X Protein / metabolism

Substances

  • Neurotoxins
  • Proto-Oncogene Proteins c-bcl-2
  • Trimethyltin Compounds
  • bcl-2-Associated X Protein
  • trimethyltin
  • Cytochromes c
  • Caspase 3