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Induction of oxidative DNA damage in U937 cells by TNF or anti-Fas stimulation

  1. Author:
    Nathan, I.
    Dizdaroglu, M.
    Bernstein, L.
    Junker, U.
    Lee, C.
    Muegge, K.
    Durum, S. K.
  2. Author Address

    Durum SK NCI, Lab Mol Immunol Frederick, MD 21702 USA NCI, Lab Mol Immunol Frederick, MD 21702 USA Natl Inst Stand & Technol, Chem Sci & Technol Lab Gaithersburg, MD 20899 USA Texas A&M Univ, Hlth Sci Ctr, Dept Pathol & Lab College Stn, TX 77843 USA NCI, SAIC Frederick, MD 21701 USA
    1. Year: 2000
  1. Journal: Cytokine
    1. 12
    2. 7
    3. Pages: 881-887
  2. Type of Article: Article
  1. Abstract:

    TNF and Fas signaling pathways are reported to induce mitochondrial damage associated with production of oxygen radicals. We examined whether such radical production elicited detectable nuclear DNA damage in U937 cells following treatment with TNF or with anti-Fas antibodies, Using GC-mass spectroscopy for analysing base oxidation, several oxidized species increased significantly following TNF treatment, whereas anti-Fas resulted in less detectable oxidative damage using this assay. Cytogenetic analysis showed that, in the presence of aphidicolin, which blocks several types of DNA repair, TNF induced extensive chromosomal damage. Aphidicolin also synergized with TNF and anti-Fas in inducing cell death which was prevented by reducing atmospheric oxygen or addition of n-acetyl cysteine, a scavenger of oxygen radicals. Thus, several lines of evidence point to the TNF and Fas pathways inducing extensive oxidative DNA damage and repair, and suggest potential roles for these pathways in mutagenesis and aging. (C) 2000 Academic Press. [References: 44]

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