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PMID: 180060 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Chemiluminescence and superoxide production by myeloperoxidase-deficient leukocytes.

The Journal of clinical investigation ·Vol. 58 ·No. 1 ·1976-07-00 ·Pages 50-60

Rosen H, Klebanoff SJ

Abstract

The role of superoxide anion- and myeloperoxidase-dependent reactions in the light emission by phagocytosing polymorphonuclear leukocytes has been investigated using leukocytes that lack myeloperoxidase, inhibitors (azide, superoxide dismutase), and model systems. Our earlier finding that oxygen consumption, glucose C-1 oxidation, and formate oxidation are greater in polymorphonuclear leukocytes that lack myeloperoxidase than in normal cells during phagocytosis has been confirmed with leukocytes from two newly described myeloperoxidase-deficient siblings. Although the maximal rate of superoxide anion production by myeloperoxidase-deficient leukocytes is not significantly different from that of normal cells, superoxide production falls off less rapidly with time so that with prolonged incubation, it is greater in myeloperoxidase-deficient than in normal cells. Chemiluminescence by myeloperoxidase-deficient leukocytes during the early postphagocytic period however is decreased. Light emission by normal leukocytes is strongly inhibited by both superoxide dismutase and azide, whereas that of myeloperoxidase-deficient leukocytes, while still strongly inhibited by superoxide dismutase is considerably less sensitive to azide. Zymosan, the phagocytic particle employed in the intact cell system, considerably increased the chemiluminescence of a cell-free superoxide-H2O2 generating system (xanthine-xanthine oxidase) and a system containing myeloperoxidase, H2O2, and chloride. Light emission by the xanthine oxidase model system is strongly inhibited by superoxide dismutase and is not inhibited by azide, whereas the myeloperoxidase-dependent model system is strongly inhibited by azide but only slightly inhibited by superoxide dismutase. These findings suggest that light emission by phagocytosing polymorphonuclear leukocytes is dependent on both myeloperoxidase-catalyzed reactions and the superoxide anion, and involves in part the excitation of the ingested particle. These studies are discussed in relation to the role of the superoxide anion and chemiluminescence in the microbicidal activity of the polymorphonuclear leukocyte.

MeSH Terms
Anions Azides/pharmacology Cell-Free System Chlorides/pharmacology Depression, Chemical Formates/metabolism Glucose/metabolism Humans Hydrogen Peroxide/pharmacology Leukocytes/enzymology,metabolism Luminescent Measurements Models, Biological Oxidation-Reduction Oxygen/biosynthesis Oxygen Consumption Peroxidase/deficiency,pharmacology Peroxidases/deficiency Superoxide Dismutase/pharmacology Superoxides/biosynthesis Xanthine Oxidase/pharmacology Xanthines/pharmacology
Chemicals
Anions Azides Chlorides Formates Xanthines Superoxides Hydrogen Peroxide Peroxidases Peroxidase Superoxide Dismutase Xanthine Oxidase Glucose Oxygen
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Rosen H
Klebanoff S J
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38 references, click to expand
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Article Info
Journal
The Journal of clinical investigation
Abbr.
J Clin Invest
ISSN
0021-9738
Published
1976-07-00
Pages
50-60
Language
English
Region
United States
NLM ID
7802877
PMCID
PMC333154
Subset
IM
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