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. 1988 Sep;82(3):1040–1050. doi: 10.1172/JCI113660

Oxidant-induced DNA damage of target cells.

I Schraufstätter 1, P A Hyslop 1, J H Jackson 1, C G Cochrane 1
PMCID: PMC303618  PMID: 2843565

Abstract

In this study we examined the leukocytic oxidant species that induce oxidant damage of DNA in whole cells. H2O2 added extracellularly in micromolar concentrations (10-100 microM) induced DNA strand breaks in various target cells. The sensitivity of a specific target cell was inversely correlated to its catalase content and the rate of removal of H2O2 by the target cell. Oxidant species produced by xanthine oxidase/purine or phorbol myristate acetate-stimulated monocytes induced DNA breakage of target cells in proportion to the amount of H2O2 generated. These DNA strand breaks were prevented by extracellular catalase, but not by superoxide dismutase. Cytotoxic doses of HOCl, added to target cells, did not induce DNA strand breakage, and myeloperoxidase added extracellularly in the presence of an H2O2-generating system, prevented the formation of DNA strand breaks in proportion to its H2O2 degrading capacity. The studies also indicated that H2O2 formed hydroxyl radical (.OH) intracellularly, which appeared to be the most likely free radical responsible for DNA damage: .OH was detected in cells exposed to H2O2; the DNA base, deoxyguanosine, was hydroxylated in cells exposed to H2O2; and intracellular iron was essential for induction of DNA strand breaks.

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Selected References

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  1. Albrich J. M., McCarthy C. A., Hurst J. K. Biological reactivity of hypochlorous acid: implications for microbicidal mechanisms of leukocyte myeloperoxidase. Proc Natl Acad Sci U S A. 1981 Jan;78(1):210–214. doi: 10.1073/pnas.78.1.210. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Althaus F. R., Lawrence S. D., Sattler G. L., Pitot H. C. ADP-ribosyltransferase activity in cultured hepatocytes. Interactions with DNA repair. J Biol Chem. 1982 May 25;257(10):5528–5535. [PubMed] [Google Scholar]
  3. Armel P. R., Strniste G. F., Wallace S. S. Studies on Escherichia coli x-ray endonuclease specificity. Roles of hydroxyl and reducing radicals in the production of DNA lesions. Radiat Res. 1977 Feb;69(2):328–338. [PubMed] [Google Scholar]
  4. Badwey J. A., Karnovsky M. L. Active oxygen species and the functions of phagocytic leukocytes. Annu Rev Biochem. 1980;49:695–726. doi: 10.1146/annurev.bi.49.070180.003403. [DOI] [PubMed] [Google Scholar]
  5. Berkow R. L., Tzeng D. Y., Williams L. V., Baehner R. L. The comparative responses of human polymorphonuclear leukocytes obtained by counterflow centrifugal elutriation and Ficoll-Hypaque density centrifugation. I. Resting volume, stimulus-induced superoxide production, and primary and specific granule release. J Lab Clin Med. 1983 Nov;102(5):732–742. [PubMed] [Google Scholar]
  6. Birnboim H. C. DNA strand breakage in human leukocytes exposed to a tumor promoter, phorbol myristate acetate. Science. 1982 Mar 5;215(4537):1247–1249. doi: 10.1126/science.6276978. [DOI] [PubMed] [Google Scholar]
  7. Birnboim H. C., Jevcak J. J. Fluorometric method for rapid detection of DNA strand breaks in human white blood cells produced by low doses of radiation. Cancer Res. 1981 May;41(5):1889–1892. [PubMed] [Google Scholar]
  8. Birnboim H. C., Kanabus-Kaminska M. The production of DNA strand breaks in human leukocytes by superoxide anion may involve a metabolic process. Proc Natl Acad Sci U S A. 1985 Oct;82(20):6820–6824. doi: 10.1073/pnas.82.20.6820. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Bradley M. O., Erickson L. C. Comparison of the effects of hydrogen peroxide and x-ray irradiation on toxicity, mutation, and DNA damage/repair in mammalian cells (V-79). Biochim Biophys Acta. 1981 Jun 26;654(1):135–141. doi: 10.1016/0005-2787(81)90146-5. [DOI] [PubMed] [Google Scholar]
  10. Brawn K., Fridovich I. DNA strand scission by enzymically generated oxygen radicals. Arch Biochem Biophys. 1981 Feb;206(2):414–419. doi: 10.1016/0003-9861(81)90108-9. [DOI] [PubMed] [Google Scholar]
  11. Brehe J. E., Burch H. B. Enzymatic assay for glutathione. Anal Biochem. 1976 Jul;74(1):189–197. doi: 10.1016/0003-2697(76)90323-7. [DOI] [PubMed] [Google Scholar]
  12. Burger R. M., Projan S. J., Horwitz S. B., Peisach J. The DNA cleavage mechanism of iron-bleomycin. Kinetic resolution of strand scission from base propenal release. J Biol Chem. 1986 Dec 5;261(34):15955–15959. [PubMed] [Google Scholar]
  13. Chance B., Sies H., Boveris A. Hydroperoxide metabolism in mammalian organs. Physiol Rev. 1979 Jul;59(3):527–605. doi: 10.1152/physrev.1979.59.3.527. [DOI] [PubMed] [Google Scholar]
  14. Cohen J. J., Duke R. C. Glucocorticoid activation of a calcium-dependent endonuclease in thymocyte nuclei leads to cell death. J Immunol. 1984 Jan;132(1):38–42. [PubMed] [Google Scholar]
  15. Fantone J. C., Ward P. A. Role of oxygen-derived free radicals and metabolites in leukocyte-dependent inflammatory reactions. Am J Pathol. 1982 Jun;107(3):395–418. [PMC free article] [PubMed] [Google Scholar]
  16. Fariss M. W., Pascoe G. A., Reed D. J. Vitamin E reversal of the effect of extracellular calcium on chemically induced toxicity in hepatocytes. Science. 1985 Feb 15;227(4688):751–754. doi: 10.1126/science.3918345. [DOI] [PubMed] [Google Scholar]
  17. Finkelstein E., Rosen G. M., Rauckman E. J. Spin trapping of superoxide and hydroxyl radical: practical aspects. Arch Biochem Biophys. 1980 Mar;200(1):1–16. doi: 10.1016/0003-9861(80)90323-9. [DOI] [PubMed] [Google Scholar]
  18. Floyd R. A., Lewis C. A. Hydroxyl free radical formation from hydrogen peroxide by ferrous iron-nucleotide complexes. Biochemistry. 1983 May 24;22(11):2645–2649. doi: 10.1021/bi00280a008. [DOI] [PubMed] [Google Scholar]
  19. Floyd R. A., Watson J. J., Harris J., West M., Wong P. K. Formation of 8-hydroxydeoxyguanosine, hydroxyl free radical adduct of DNA in granulocytes exposed to the tumor promoter, tetradecanoylphorbolacetate. Biochem Biophys Res Commun. 1986 Jun 13;137(2):841–846. doi: 10.1016/0006-291x(86)91156-3. [DOI] [PubMed] [Google Scholar]
  20. Floyd R. A., Watson J. J., Wong P. K. Sensitive assay of hydroxyl free radical formation utilizing high pressure liquid chromatography with electrochemical detection of phenol and salicylate hydroxylation products. J Biochem Biophys Methods. 1984 Dec;10(3-4):221–235. doi: 10.1016/0165-022x(84)90042-3. [DOI] [PubMed] [Google Scholar]
  21. Goldstein S., Czapski G. The role and mechanism of metal ions and their complexes in enhancing damage in biological systems or in protecting these systems from the toxicity of O2-. J Free Radic Biol Med. 1986;2(1):3–11. doi: 10.1016/0748-5514(86)90117-0. [DOI] [PubMed] [Google Scholar]
  22. Griffith O. W. Determination of glutathione and glutathione disulfide using glutathione reductase and 2-vinylpyridine. Anal Biochem. 1980 Jul 15;106(1):207–212. doi: 10.1016/0003-2697(80)90139-6. [DOI] [PubMed] [Google Scholar]
  23. Griffith O. W., Meister A. Potent and specific inhibition of glutathione synthesis by buthionine sulfoximine (S-n-butyl homocysteine sulfoximine). J Biol Chem. 1979 Aug 25;254(16):7558–7560. [PubMed] [Google Scholar]
  24. Guilbault G. G., Brignac P. J., Jr, Juneau M. New substrates for the fluorometric determination of oxidative enzymes. Anal Chem. 1968 Jul;40(8):1256–1263. doi: 10.1021/ac60264a027. [DOI] [PubMed] [Google Scholar]
  25. Gutteridge J. M. Ferrous-salt-promoted damage to deoxyribose and benzoate. The increased effectiveness of hydroxyl-radical scavengers in the presence of EDTA. Biochem J. 1987 May 1;243(3):709–714. doi: 10.1042/bj2430709. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Halliwell B., Gutteridge J. M. Oxygen free radicals and iron in relation to biology and medicine: some problems and concepts. Arch Biochem Biophys. 1986 May 1;246(2):501–514. doi: 10.1016/0003-9861(86)90305-x. [DOI] [PubMed] [Google Scholar]
  27. Hinshaw D. B., Sklar L. A., Bohl B., Schraufstatter I. U., Hyslop P. A., Rossi M. W., Spragg R. G., Cochrane C. G. Cytoskeletal and morphologic impact of cellular oxidant injury. Am J Pathol. 1986 Jun;123(3):454–464. [PMC free article] [PubMed] [Google Scholar]
  28. Hutchinson F. Chemical changes induced in DNA by ionizing radiation. Prog Nucleic Acid Res Mol Biol. 1985;32:115–154. doi: 10.1016/s0079-6603(08)60347-5. [DOI] [PubMed] [Google Scholar]
  29. Hyslop P. A., Hinshaw D. B., Halsey W. A., Jr, Schraufstätter I. U., Sauerheber R. D., Spragg R. G., Jackson J. H., Cochrane C. G. Mechanisms of oxidant-mediated cell injury. The glycolytic and mitochondrial pathways of ADP phosphorylation are major intracellular targets inactivated by hydrogen peroxide. J Biol Chem. 1988 Feb 5;263(4):1665–1675. [PubMed] [Google Scholar]
  30. Hyslop P. A., Hinshaw D. B., Schraufstätter I. U., Sklar L. A., Spragg R. G., Cochrane C. G. Intracellular calcium homeostasis during hydrogen peroxide injury to cultured P388D1 cells. J Cell Physiol. 1986 Dec;129(3):356–366. doi: 10.1002/jcp.1041290314. [DOI] [PubMed] [Google Scholar]
  31. Hyslop P. A., Sklar L. A. A quantitative fluorimetric assay for the determination of oxidant production by polymorphonuclear leukocytes: its use in the simultaneous fluorimetric assay of cellular activation processes. Anal Biochem. 1984 Aug 15;141(1):280–286. doi: 10.1016/0003-2697(84)90457-3. [DOI] [PubMed] [Google Scholar]
  32. Jackson J. H., Schraufstatter I. U., Hyslop P. A., Vosbeck K., Sauerheber R., Weitzman S. A., Cochrane C. G. Role of oxidants in DNA damage. Hydroxyl radical mediates the synergistic DNA damaging effects of asbestos and cigarette smoke. J Clin Invest. 1987 Oct;80(4):1090–1095. doi: 10.1172/JCI113165. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Johnson K. J., Fantone J. C., 3rd, Kaplan J., Ward P. A. In vivo damage of rat lungs by oxygen metabolites. J Clin Invest. 1981 Apr;67(4):983–993. doi: 10.1172/JCI110149. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Kasai H., Nishimura S. Hydroxylation of deoxyguanosine at the C-8 position by ascorbic acid and other reducing agents. Nucleic Acids Res. 1984 Feb 24;12(4):2137–2145. doi: 10.1093/nar/12.4.2137. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Kensler T. W., Bush D. M., Kozumbo W. J. Inhibition of tumor promotion by a biomimetic superoxide dismutase. Science. 1983 Jul 1;221(4605):75–77. doi: 10.1126/science.6857269. [DOI] [PubMed] [Google Scholar]
  36. Klein S. M., Cohen G., Cederbaum A. I. Production of formaldehyde during metabolism of dimethyl sulfoxide by hydroxyl radical generating systems. Biochemistry. 1981 Oct 13;20(21):6006–6012. doi: 10.1021/bi00524a013. [DOI] [PubMed] [Google Scholar]
  37. Kuchino Y., Mori F., Kasai H., Inoue H., Iwai S., Miura K., Ohtsuka E., Nishimura S. Misreading of DNA templates containing 8-hydroxydeoxyguanosine at the modified base and at adjacent residues. Nature. 1987 May 7;327(6117):77–79. doi: 10.1038/327077a0. [DOI] [PubMed] [Google Scholar]
  38. Lesko S. A., Lorentzen R. J., Ts'o P. O. Role of superoxide in deoxyribonucleic acid strand scission. Biochemistry. 1980 Jun 24;19(13):3023–3028. doi: 10.1021/bi00554a029. [DOI] [PubMed] [Google Scholar]
  39. Lynch R. E., Fridovich I. Permeation of the erythrocyte stroma by superoxide radical. J Biol Chem. 1978 Jul 10;253(13):4697–4699. [PubMed] [Google Scholar]
  40. McWilliams R. S., Cross W. G., Kaplan J. G., Birnboim H. C. Rapid rejoining of DNA strand breaks in resting human lymphocytes after irradiation by low doses of 60Co gamma rays or 14.6-MeV neutrons. Radiat Res. 1983 Jun;94(3):499–507. [PubMed] [Google Scholar]
  41. Nathan C. F., Brukner L. H., Silverstein S. C., Cohn Z. A. Extracellular cytolysis by activated macrophages and granulocytes. I. Pharmacologic triggering of effector cells and the release of hydrogen peroxide. J Exp Med. 1979 Jan 1;149(1):84–99. doi: 10.1084/jem.149.1.84. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Nathan C. F., Silverstein S. C., Brukner L. H., Cohn Z. A. Extracellular cytolysis by activated macrophages and granulocytes. II. Hydrogen peroxide as a mediator of cytotoxicity. J Exp Med. 1979 Jan 1;149(1):100–113. doi: 10.1084/jem.149.1.100. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. O'Donnell-Tormey J., DeBoer C. J., Nathan C. F. Resistance of human tumor cells in vitro to oxidative cytolysis. J Clin Invest. 1985 Jul;76(1):80–86. doi: 10.1172/JCI111981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Omann G. M., Swann W. N., Oades Z. G., Parkos C. A., Jesaitis A. J., Sklar L. A. N-formylpeptide-receptor dynamics, cytoskeletal activation, and intracellular calcium response in human neutrophil cytoplasts. J Immunol. 1987 Nov 15;139(10):3447–3455. [PubMed] [Google Scholar]
  45. Paglia D. E., Valentine W. N. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clin Med. 1967 Jul;70(1):158–169. [PubMed] [Google Scholar]
  46. Revak S. D., Rice C. L., Schraufstätter I. U., Halsey W. A., Jr, Bohl B. P., Clancy R. M., Cochrane C. G. Experimental pulmonary inflammatory injury in the monkey. J Clin Invest. 1985 Sep;76(3):1182–1192. doi: 10.1172/JCI112074. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Richmond R., Halliwell B., Chauhan J., Darbre A. Superoxide-dependent formation of hydroxyl radicals: detection of hydroxyl radicals by the hydroxylation of aromatic compounds. Anal Biochem. 1981 Dec;118(2):328–335. doi: 10.1016/0003-2697(81)90590-x. [DOI] [PubMed] [Google Scholar]
  48. Roos D., Voetman A. A., Meerhof L. J. Functional activity of enucleated human polymorphonuclear leukocytes. J Cell Biol. 1983 Aug;97(2):368–377. doi: 10.1083/jcb.97.2.368. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Roos D., Weening R. S., Wyss S. R., Aebi H. E. Protection of human neutrophils by endogenous catalase: studies with cells from catalase-deficient individuals. J Clin Invest. 1980 Jun;65(6):1515–1522. doi: 10.1172/JCI109817. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Roots R., Okada S. Estimation of life times and diffusion distances of radicals involved in x-ray-induced DNA strand breaks of killing of mammalian cells. Radiat Res. 1975 Nov;64(2):306–320. [PubMed] [Google Scholar]
  51. Sacks T., Moldow C. F., Craddock P. R., Bowers T. K., Jacob H. S. Oxygen radicals mediate endothelial cell damage by complement-stimulated granulocytes. An in vitro model of immune vascular damage. J Clin Invest. 1978 May;61(5):1161–1167. doi: 10.1172/JCI109031. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Schraufstatter I. U., Hinshaw D. B., Hyslop P. A., Spragg R. G., Cochrane C. G. Oxidant injury of cells. DNA strand-breaks activate polyadenosine diphosphate-ribose polymerase and lead to depletion of nicotinamide adenine dinucleotide. J Clin Invest. 1986 Apr;77(4):1312–1320. doi: 10.1172/JCI112436. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Schraufstatter I. U., Hyslop P. A., Hinshaw D. B., Spragg R. G., Sklar L. A., Cochrane C. G. Hydrogen peroxide-induced injury of cells and its prevention by inhibitors of poly(ADP-ribose) polymerase. Proc Natl Acad Sci U S A. 1986 Jul;83(13):4908–4912. doi: 10.1073/pnas.83.13.4908. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Schraufstätter I. U., Hinshaw D. B., Hyslop P. A., Spragg R. G., Cochrane C. G. Glutathione cycle activity and pyridine nucleotide levels in oxidant-induced injury of cells. J Clin Invest. 1985 Sep;76(3):1131–1139. doi: 10.1172/JCI112068. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Schraufstätter I. U., Revak S. D., Cochrane C. G. Proteases and oxidants in experimental pulmonary inflammatory injury. J Clin Invest. 1984 Apr;73(4):1175–1184. doi: 10.1172/JCI111303. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Simon R. H., Scoggin C. H., Patterson D. Hydrogen peroxide causes the fatal injury to human fibroblasts exposed to oxygen radicals. J Biol Chem. 1981 Jul 25;256(14):7181–7186. [PubMed] [Google Scholar]
  57. Slater T. F. Free-radical mechanisms in tissue injury. Biochem J. 1984 Aug 15;222(1):1–15. doi: 10.1042/bj2220001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. Spragg R. G., Hinshaw D. B., Hyslop P. A., Schraufstätter I. U., Cochrane C. G. Alterations in adenosine triphosphate and energy charge in cultured endothelial and P388D1 cells after oxidant injury. J Clin Invest. 1985 Oct;76(4):1471–1476. doi: 10.1172/JCI112126. [DOI] [PMC free article] [PubMed] [Google Scholar]
  59. Stoewe R., Prütz W. A. Copper-catalyzed DNA damage by ascorbate and hydrogen peroxide: kinetics and yield. Free Radic Biol Med. 1987;3(2):97–105. doi: 10.1016/s0891-5849(87)80003-5. [DOI] [PubMed] [Google Scholar]
  60. Thurman R. G., Ley H. G., Scholz R. Hepatic microsomal ethanol oxidation. Hydrogen peroxide formation and the role of catalase. Eur J Biochem. 1972 Feb;25(3):420–430. doi: 10.1111/j.1432-1033.1972.tb01711.x. [DOI] [PubMed] [Google Scholar]
  61. Till G. O., Johnson K. J., Kunkel R., Ward P. A. Intravascular activation of complement and acute lung injury. Dependency on neutrophils and toxic oxygen metabolites. J Clin Invest. 1982 May;69(5):1126–1135. doi: 10.1172/JCI110548. [DOI] [PMC free article] [PubMed] [Google Scholar]
  62. Ueda K., Kobayashi S., Morita J., Komano T. Site-specific DNA damage caused by lipid peroxidation products. Biochim Biophys Acta. 1985 Apr 19;824(4):341–348. doi: 10.1016/0167-4781(85)90041-7. [DOI] [PubMed] [Google Scholar]
  63. Weiss S. J., Young J., LoBuglio A. F., Slivka A., Nimeh N. F. Role of hydrogen peroxide in neutrophil-mediated destruction of cultured endothelial cells. J Clin Invest. 1981 Sep;68(3):714–721. doi: 10.1172/JCI110307. [DOI] [PMC free article] [PubMed] [Google Scholar]
  64. Weitberg A. B., Weitzman S. A., Clark E. P., Stossel T. P. Effects of antioxidants on oxidant-induced sister chromatid exchange formation. J Clin Invest. 1985 Jun;75(6):1835–1841. doi: 10.1172/JCI111897. [DOI] [PMC free article] [PubMed] [Google Scholar]
  65. Weitzman S. A., Weitberg A. B., Clark E. P., Stossel T. P. Phagocytes as carcinogens: malignant transformation produced by human neutrophils. Science. 1985 Mar 8;227(4691):1231–1233. doi: 10.1126/science.3975611. [DOI] [PubMed] [Google Scholar]
  66. Weitzman S. A., Weitberg A. B., Clark E. P., Stossel T. P. Phagocytes as carcinogens: malignant transformation produced by human neutrophils. Science. 1985 Mar 8;227(4691):1231–1233. doi: 10.1126/science.3975611. [DOI] [PubMed] [Google Scholar]
  67. Winterbourn C. C., Hawkins R. E., Brian M., Carrell R. W. The estimation of red cell superoxide dismutase activity. J Lab Clin Med. 1975 Feb;85(2):337–341. [PubMed] [Google Scholar]
  68. Zimmerman R., Cerutti P. Active oxygen acts as a promoter of transformation in mouse embryo C3H/10T1/2/C18 fibroblasts. Proc Natl Acad Sci U S A. 1984 Apr;81(7):2085–2087. doi: 10.1073/pnas.81.7.2085. [DOI] [PMC free article] [PubMed] [Google Scholar]
  69. de Mello Filho A. C., Meneghini R. Protection of mammalian cells by o-phenanthroline from lethal and DNA-damaging effects produced by active oxygen species. Biochim Biophys Acta. 1985 Oct 30;847(1):82–89. doi: 10.1016/0167-4889(85)90156-9. [DOI] [PubMed] [Google Scholar]
  70. deAlvare L. R., Goda K., Kimura T. Mechanism of superoxide anion scavenging reaction by bis-(salicylato)-copper (II) complex. Biochem Biophys Res Commun. 1976 Apr 5;69(3):687–694. doi: 10.1016/0006-291x(76)90930-x. [DOI] [PubMed] [Google Scholar]
  71. van Steveninck J., van der Zee J., Dubbelman T. M. Site-specific and bulk-phase generation of hydroxyl radicals in the presence of cupric ions and thiol compounds. Biochem J. 1985 Nov 15;232(1):309–311. doi: 10.1042/bj2320309. [DOI] [PMC free article] [PubMed] [Google Scholar]

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