Peroxynitrite damages U937 cell DNA via the intermediate formation of mitochondrial oxidants

IUBMB Life. 2008 Nov;60(11):753-6. doi: 10.1002/iub.116.

Abstract

Eight years ago, we published in this journal the first evidence that peroxynitrite does not directly produce DNA single-strand breakage in intact U937 cells (Guidarelli et al., IUBMB Life, 50, 195-201). This event was rather attributed to the secondary reactive species produced at the mitochondrial level via a Ca2+-dependent reaction, in which ubisemiquinone serves as an electron donor. Under these conditions, electrons are directly transferred to molecular oxygen and superoxide/H2O2, and the ensuing DNA damage can therefore be produced in a time- dependent manner for at least 30 min. Formation of H2O2 and DNA single-strand breaks was therefore dependent on interference with electron transport at the complex III level as well as on mitochondrial Ca2+ accumulation. Further studies led to the demonstrations that peroxynitrite mobilizes Ca2+ from the ryanodine receptor. Finally, in U937 cells, a pro-monocytic cell line sharing with monocytes/macrophages the same signaling events to survive to peroxynitrite, mitochondrial H2O2 promotes inhibition of survival via tyrosine phosphatase activation, leading to ERK1/2 dephosphorylation and thus to upstream inhibition of the survival signaling.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Calcium / metabolism
  • DNA Damage*
  • DNA, Mitochondrial / metabolism
  • DNA, Single-Stranded / metabolism
  • Electron Transport / drug effects
  • Humans
  • Hydrogen Peroxide / pharmacology
  • Mitochondria / drug effects*
  • Mitochondria / metabolism
  • Models, Biological
  • Oxidants / metabolism*
  • Oxidants / pharmacology*
  • Peroxynitrous Acid / pharmacology*
  • Ryanodine / pharmacology
  • Superoxides / metabolism
  • U937 Cells

Substances

  • DNA, Mitochondrial
  • DNA, Single-Stranded
  • Oxidants
  • Superoxides
  • Peroxynitrous Acid
  • Ryanodine
  • Hydrogen Peroxide
  • Calcium