The production of DNA strand breaks in human leukocytes by superoxide anion may involve a metabolic process
Autor: | H C Birnboim, M Kanabus-Kaminska |
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Rok vydání: | 1985 |
Předmět: |
DNA Replication
DNA damage Deoxyglucose Superoxide dismutase chemistry.chemical_compound Reference Values Superoxides Leukocytes Extracellular Humans Calcimycin Multidisciplinary biology Superoxide Dismutase Chemistry Superoxide DNA replication DNA Catalase Kinetics Biochemistry biology.protein Sodium Fluoride Intracellular Research Article Phenanthrolines |
Zdroj: | Proceedings of the National Academy of Sciences. 82:6820-6824 |
ISSN: | 1091-6490 0027-8424 |
DOI: | 10.1073/pnas.82.20.6820 |
Popis: | H2O2 is known to be capable of inducing strand-break damage in intracellular DNA, but whether O2- also can do so in the absence of H2O2 is uncertain. The difficulty in distinguishing the effects of the two is that, under physiological conditions, dismutation of O2- to H2O2 can readily occur. When human leukocytes are stimulated with phorbol 12-myristate 13-acetate (PMA), they release O2-, and within a few minutes strand breakage in intracellular DNA can be observed. We have attempted to determine whether the O2- produced is itself capable of causing DNA damage or whether H2O2 alone, or in combination with O2-, is responsible for the observed damage. Addition of catalase (up to 250 micrograms/ml) to remove H2O2 prevented no more than about 50% of the DNA damage. The majority of the remaining damage could be blocked, in a dose-dependent manner, by superoxide dismutase (SOD) or a SOD-mimetic copper complex, identifying a fraction of damage to intracellular DNA dependent upon extracellular O2-. We studied this O2(-)-specific fraction through the use of three metabolic poisons (fluoride, 2-deoxyglucose, and A23187). These agents largely blocked DNA damage, while affecting extracellular O2- levels only slightly. For comparison, H2O2-induced DNA damage was studied with glucose oxidase to generate a flux of H2O2. The first two metabolic poisons had little effect, whereas A23187 did inhibit H2O2-induced DNA damage. We conclude that O2(-)-induced damage occurs through a mechanism that differs, at least in part, from the H2O2 damage pathway and that the former may involve one or more metabolic steps. |
Databáze: | OpenAIRE |
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