The Influence of Superoxide on the Production of Hypochlorous Acid by Human Neutrophils

References

• Weiss S. J., LoBuglio A. F. Phagocyte-generated oxygen metabolites and cellular injury. Laboratory Investigation. 1982; 47: 5–18
   PubMed Web of Science ®Google Scholar
• Weiss S. J., Klein R., Slivka A., Wei M. Chlorination of taurine by human neutrophils. Evidence for hypochlorous acid generation. Journal of Clinical Investigation. 1982; 70: 598–607
   PubMed Web of Science ®Google Scholar
• Footc C. S., Goyne T. E., Lehrer R. I. Assessment of chlorination by human neutrophils. Nature 1953; 301: 715–716
   Google Scholar
• Harrison J. E., Schultz J. Studies on the chlorinating activity of myeloperoxidase. Jouranl of Biological Chemistry. 1976; 251: 1371–1374
   PubMed Web of Science ®Google Scholar
• Makino R., Tanaka T., Iizuka T., Ishimura Y., Kancgasaki S. Stoichiometric conversion of oxygen to superoxide anion during the respiratory burst in neutrophils. Journal of Biological Chemistry. 1986; 261: 11444–11447
   PubMedGoogle Scholar
• Odajima Y., Yamazaki I. Myeloperoxidase of the leukocytes of normal blood. III The reaction of ferric myeloperoxidase with superoxide anion. Biochimica Biophysica Acta. 1972; 284: 355–359
   PubMedGoogle Scholar
• Kettle A. J., Winterbourn C. C. Superoxide modulates the activity of myeloperoxidase and optimizes the production of hypochlorous acid. Biochemical Journal. 1988; 252: 529–536
   PubMed Web of Science ®Google Scholar
• Kettle A. J., Winterbourn C. C. The influence of superoxide on the kinetics of myeloperoxidase measured with a H2O2 electrode. Biochemical Journal. 1989; 263: 823–828
   PubMed Web of Science ®Google Scholar
• Winterbourn C. C., Garcia R., Segal A. W. Production of the superoxide adduct of myeloperoxidase (compound III) by stimulated neutrophils and its reactivity with hydrogen peroxide and chloride. Biocliemical Journal. 1985; 228: 583–592
   PubMed Web of Science ®Google Scholar
• Clark R. A., Stone P. J., El-hag A., Calore J. D., Franzblau C. Myeloperoxidasecatalysed inactivation of α1 -protease inhibitor by human neutrophils. The Journal of Biological Chemistry. 1981; 256: 3348–3353
   PubMed Web of Science ®Google Scholar
• Kettle A. J., Winterbourn C. C. Superoxide enhances the production of hypochlorous acid by stimulated human neutrophils. BBA 1990, In Press.
   PubMedGoogle Scholar
• Boyum A. Isolation of mononuclear cells and granulocytes from human blood. Isolation of mononuclear cells by one centrifugation; and of granulocytes by combining centrifugation and sedimentation at Ig. Scandinavian Journal of Clinical Investigation (Suppl.) 1968; 21: 77–89
   PubMed Web of Science ®Google Scholar
• Odajima T., Yamazaki I. Myeloperoxidase of the leukocytes of normal blood. I. Reaction of myeloperoxidase with hydrogen peroxide. Biochimica Biophysica Acta. 1970; 206: 71–77
   PubMedGoogle Scholar
• Hager L. P., Morris D. R., Brown F. S., Ebenvein H. Chloroperoxidase. II. Utilization of halogen ions. The Journal of Biological Chemistry. 1966; 241: 1769–1777
   PubMed Web of Science ®Google Scholar
• Halliwell B., Gutteridge J. M. C. Free radicals in human disease. Molecular Aspects of Medicine. 1985; 8: 89–193
   PubMed Web of Science ®Google Scholar
• Tsan M. F. Myeloperoxidase-mediated oxidation of methionine and amino acid decarboxylation. Infection and Immunisation 1982; 36: 136–141
   PubMedGoogle Scholar
• Winterbourn C. C. Comparative reactivities of various biological compounds with myeloperoxidase-hydrogen peroxidechloride, and similarity of the oxidant to hypochlorite. Biochimica Biophysica Acta 1985; 840: 204–210
   PubMed Web of Science ®Google Scholar
• Bolscher B. G. J. M., Zoutberg G. R., Cuperus R. A., Wever R. Vitamin C stimulates the chlorinating activity of human myeloperoxidase. Bicohimica Biopliysica Acta. 1984; 784: 189–191
   PubMed Web of Science ®Google Scholar
• Kettle A. J., Winterbourn C. C. The mechanism of myeloperoxidase-dependent chlorination of monochlorodimedon. Biochimica Biophysica Acta. 1988; 957: 185–181
   PubMed Web of Science ®Google Scholar
• Cohen M. S., Britigan B. E., Hassett D. J., Rosen G. M. Do human neutrophils form hydroxyl radical? Evaluation of an unresolved controversy. Free Radical Biological Medicine 1988; 5: 81–88
   PubMed Web of Science ®Google Scholar
• Winterbourn C. C. Myeloperoxidase as an effective inhibitor of hydroxyl radical production. The Journal of Clinical Invesligalion. 1986; 18: 545–550
   Google Scholar
• Salin M. L., McCord J. M. Free radicals and inflammation: Protection of phagocytosing leukocytes by superoxide disrnutase. The Journal of Clinical Invesrigarion. 1975; 56: 1319–1323
   PubMed Web of Science ®Google Scholar
• Johnston R. B., Jr., Keele B. B., Jr., Misra H., Lehmeyer J. E., Webb L. S., Haehner R. L., Rajagopalan K. V. The role of superoxide anion generation in phagocytic bactericidial activity. Studies with normal and chronic granulomatous disease leukocytes. The Journal of Clinical Invesligalion. 1975; 55: 1357–1372
   PubMed Web of Science ®Google Scholar
• Sasada M., Kubo A., Nishimura T., Kakita T., Moriguchi T., Yamamoto K., Uchino H. Canadacidal activity of monocyte-derived human niacrophages. Relationship between candidal killing and oxygen radical generation by human macrophages. Journal pf Lcukocyte Biology 1987; 41: 289–294
   PubMed Web of Science ®Google Scholar