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. 1973 Mar;52(3):741-4.
doi: 10.1172/JCI107236.

Biological defense mechanisms. The production by leukocytes of superoxide, a potential bactericidal agent

Biological defense mechanisms. The production by leukocytes of superoxide, a potential bactericidal agent

B M Babior et al. J Clin Invest. 1973 Mar.

Abstract

As a highly reactive substance produced in biological systems by the one-electron reduction of oxygen, superoxide (O(2) (-)) seemed a likely candidate as a bactericidal agent in leukocytes. The reduction of cytochrome c, a process in which O(2) (-) may serve as an electron donor, was found to occur when the cytochrome was incubated with leukocytes. O(2) (-) was identified as the agent responsible for the leukocyte-mediated reduction of cytochrome c by the demonstration that the reaction was abolished by superoxide dismutase, an enzyme that destroys O(2) (-), but not by boiled dismutase, albumin, or catalase. Leukocyte O(2) (-) production doubled in the presence of latex particles. The average rate of formation of O(2) (-) in the presence of these particles was 1.03 nmol/10(7) cells per 15 min. This rate, however, is only a lower limit of the true rate of O(2) (-) production, since any O(2) (-) which reacted with constituents other than cytochrome c would have gone undetected. Thus. O(2) (-) is made by leukocytes under circumstances which suggest that it may be involved in bacterial killing.

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References

    1. J Exp Med. 1967 Dec 1;126(6):1063-78 - PubMed
    1. Biochim Biophys Acta. 1968 Feb 1;156(1):168-78 - PubMed
    1. Semin Hematol. 1968 Apr;5(2):156-65 - PubMed
    1. J Bacteriol. 1969 Jun;98(3):996-1004 - PubMed
    1. J Biol Chem. 1969 Nov 25;244(22):6049-55 - PubMed