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  • Title: A novel mechanism, uniquely dependent on mitochondrial calcium accumulation, whereby peroxynitrite promotes formation of superoxide/hydrogen peroxide and the ensuing strand scission of genomic DNA.
    Author: Guidarelli A, Fiorani M, Azzolini C, Cantoni O.
    Journal: Antioxid Redox Signal; 2010 Sep 15; 13(6):745-56. PubMed ID: 20136509.
    Abstract:
    High concentrations of peroxynitrite elicit delayed formation of DNA-damaging species through a mechanism dependent on mitochondrial Ca(2+) accumulation and inhibition of complex III. A second mechanism, requiring remarkably lower peroxynitrite concentrations, is observed in the presence of bona fide complex III inhibitors and is Ca(2+) independent. We now report evidence for a third mechanism, also operative with low peroxynitrite concentrations, independent of electron transport, and entirely based on mitochondrial Ca(2+) accumulation. This concept was established by using permeabilized respiration-proficient and -deficient U937 cells supplemented with Ca(2+), inhibitors of mitochondrial Ca(2+) accumulation, and specific respiratory-chain inhibitors. The results obtained were validated by experiments performed with intact cells, by using caffeine (Cf ) to promote mitochondrial Ca(2+) accumulation. Under these conditions, low concentrations of peroxynitrite, otherwise unable to generate detectable DNA cleavage, caused maximal DNA strand scission through a mechanism insensitive to respiratory-chain inhibitors or to the respiration-deficient phenotype. The effects of Cf were mimicked by other ryanodine receptor agonists, were suppressed by ryanodine, and were not observed in cells failing to express the ryanodine receptor, as differentiated U937 cells or human monocytes. This study provides evidence for a novel mechanism whereby peroxynitrite may indirectly mediate DNA strand scission under inflammatory conditions.
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