Alterations of the Oxidative Metabolism and Other Microbicidal Activities of Human Polymorphonuclear Leukocytes By Zinc

References

• Mills C. F. Biochemical roles of trace elements. Progression in Clinical Biology Research 1981; 77: 179–188
   Google Scholar
• Macartney H. W., Tschesche H. The metal ion requirement for activation of latent collagenase from human polymorpho-nuclcar leukocytes. Hoppe-Sevleh Z. Physiol. Chem. 1981; 362: 1523–1531
   Google Scholar
• Gainer J. H. Effects of heavy metals and the deficiency of zinc on mortality rates in mice infected with encephalomyocarditis virus. American Journal of Veterinary Research 1977; 38: 869–872
   PubMed Web of Science ®Google Scholar
• Evans G. W. Zinc and its deficiency diseases. Clinical Physiology of Biochemistry 1986; 4: 94–98
   PubMedGoogle Scholar
• Haynes D. C., Gershwin M. E., Golub M. S., Cheung A., Hurley L. S., Hendrickx A. Studies of marginal zinc deprivation in rhesus monkeys: VI. Influence on the immunohematology of infants in the first year. American Journal of Clinical Nutrition 1985; 42: 252–262
   PubMedGoogle Scholar
• Chandra R. K., Dayton D. H. Trace clement regulation of immunity and infection. Nutrition Research 1982; 2: 721–733
   Web of Science ®Google Scholar
• Koller L. D. Immunotoxicology of heavy metals. Internation Journal of Immunopharmacology 1980; 2: 269–279
   PubMed Web of Science ®Google Scholar
• Chandra R. K. Excessive intake of zinc impairs immune responses. JAMA 1984; 252: 1443–1446
   PubMed Web of Science ®Google Scholar
• Yatsuyanagi J., Iwai K., Ogiso T. Suppressive effect of zinc on some functions of neutrophils: Studies with carrageenan-induced inflammation in rats. Chemistry and Pharmacology Bulletin 1987; 35: 699–704
   Google Scholar
• Skornik W. A., Brain J. D. Relative toxicity of inhaled metal sulfate salts for pulmonary macrophages. American Review of Respiratory Disease 1983; 128: 297–303
   PubMedGoogle Scholar
• Chvapil M., Stankova L., Zukoski Ch., IV, Zukoski Ch., III. Inhibition of some functions of polymorphonuclear leukocytes by in vitro zinc. Journal of Laboratory Clinical Medicine 1977; 89: 135–146
   PubMed Web of Science ®Google Scholar
• Babior B. M. Oxygen-dependent microbial killing by phagocytes. New England Journal of Medicine. 1978; 298: 659–668
   PubMed Web of Science ®Google Scholar
• Fridovich I. Superoxide radical and the bactericidal action of phagocytes. New England Journal Medicine 1974; 290: 624–625
   Google Scholar
• Beswick P. H., Brannen P. C., Hurles S. S. The effects of smoking and zinc on the oxidative reactions of human neutrophils. Journal of Clinical Laboratory Immunology 1986; 21: 71–75
   Google Scholar
• Amoruso M. A., Witz G., Goldstein B. D. Enhancement of rat and human phagocyte superoxide anion radical production by cadmium in vitro. Toxicology Letters 1982; 10: 133–138
   PubMed Web of Science ®Google Scholar
• Malamud D., Scott A., Shapiro D., Shapiro I. M. Low levels of mercury inhibit the respiratory burst in human polymorphonuclear leukocytes. Biochemistry and Biophysics Research Communications 1985; 128: 1145–1151
   PubMed Web of Science ®Google Scholar
• Bainton D. F. Sequential degranulation of the two types of polymorphonuclear leukocyte granules during phagocytosis of microorganisms. Journal of Cell Biology 1973; 58: 249–264
   PubMed Web of Science ®Google Scholar
• Böyum A. Isolation of mononuclear cells and granulocytes from human blood. Scandanavian Journal of Clinical Laboratory Investigation 1968; 21: 77–89
   PubMed Web of Science ®Google Scholar
• Baginski B. Einfluβ von Blei und Cadmium auf die Vitalität und Phagozytosefähigkeit humaner polymorphkerniger Leukozyten. Zbl. Bakt. Hyg., I. Abt. Orig. 1985; B 181: 461–468
   Google Scholar
• Schmid L., Brune K. Assessment of phagocytic and antimicrobial activity of human granulocytes. Infection and Immunity 1974; 10: 1120–1126
   PubMed Web of Science ®Google Scholar
• Goldstein I. M., Roos D., Kaplan H. B., Weissmann G. J. Complement and immunoglobulins stimulate superoxide production by human leukocytes independently of phagocytosis. Clinical Investigation 1975; 56: 1155–1163
   Google Scholar
• Baginski B. Effect of mercuric chloride on microbicidal activities of human polymorphonuclear leukocytes. Toxicology. 1988; 50: 247–256
   PubMedGoogle Scholar
• Hildebrandt A. G., Roots I. Reduced Nicotinamide adenine dinucleotide phosphate (NAD-PH)-dependent formation and breakdown of hydrogen peroxide during mixed function oxidation reactions in liver microsomes. Archives of Biochemistry and Biophysics 1975; 171: 385–397
   PubMed Web of Science ®Google Scholar
• Allen R. C., Loose L. D. Phagocytic activation of a luminol-dependent chemiluminescence in rabbit alveolar and peritoneal macrophages. Biochemistry and Biophysics Research Communications 1976; 69: 245–252
   PubMed Web of Science ®Google Scholar
• Dahlgren C., Stendahl O. Role of myeloperoxidase in luminol-dependent chemiluminescence of polymorphonuclear leukocytes. Infection and Immunity 1983; 39: 736–741
   PubMed Web of Science ®Google Scholar
• Allen R. C. Lucigenin chemiluminescence: A new approach to the study of polymorphonuclear leukocyte redox activity. Bioluminescence and Chemiluminescence, M. A. DeLuca, W. D. McElroy. Academic Press, New York 1981; 63–72
   Google Scholar
• Gyllenhammar H. Lucigenin chemiluminescence in the assessment of neutrophil superoxide production. Journal of Immunology Methods 1987; 97: 209–213
   PubMed Web of Science ®Google Scholar
• Versieck J., Barbier F., Speecke A., Hoste J. Plasma-zinc levels. The Lancet 1974; 682
   Google Scholar
• Venge P., Hällgren R., Stalenheim G., Olsson I. Effects of serum and cations on the selective release of granular proteins from human neutrophils during phagocytosis. Scandanavian Journal of Haematologv 1979; 22: 317–326
   PubMedGoogle Scholar
• de Chatelet L. R., Lees C. J., Walsh C. E., Long G. D., Shirley P. S. Comparison of the calcium ionophore and phorbol myristatc acetate on the initiation of the respiratory burst in human neutrophils. Infection and Immunity 1982; 38: 969–974
   Google Scholar
• Bender J. G., van Epps D. E. Stimulus interactions in release of superoxide anion (O2−) from human neutrophils. Further evidence for multiple pathways of activation. Inflammation 1985; 9: 67–79
   Google Scholar
• Christiansen N. O., Larsen C. S., Juhl H., Esmann V. Membrane-associated protein kinase C activity in superoxide-producing human polymorphonuclear leukocytes. Journal of Leukocyte Biology. 1988; 44: 33–40
   Google Scholar
• Nishihira J., O'Flaherty J. T. Phorbol myristate acetate receptors in human polymorphonuclear neutrophils. Journal of Immunology 1985; 135: 3439–3447
   Google Scholar
• Baginski B., Holzwig D., Helmrich R. Lead effects on human polymorphonuclear leukocytes - promotion of inflammatory reactions?. Heavy metals in the hydrological cycle, M. Astruc, J. N. Lester. Selper Ltd., London 1988; 35–40
   Google Scholar
• Sacks T., Moldow Ch. F., Craddock Ph. R., Bowers T. K., Jakob H. S. Oxygen radicals mediate endothelial cell damage by complement- stimulated granulocytes. Journal of Clinical Investigation 1978; 61: 1161–1167
   PubMed Web of Science ®Google Scholar
• Ward P. A. Role of toxic oxygen products from phagocytic cells in tissue injury. Advances in Shock Research 1983; 10: 27–34
   PubMedGoogle Scholar