Chemiluminescence and superoxide production by myeloperoxidase-deficient leukocytes.
Open Access
- 1 July 1976
- journal article
- research article
- Published by American Society for Clinical Investigation in Journal of Clinical Investigation
- Vol. 58 (1) , 50-60
- https://doi.org/10.1172/jci108458
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.This publication has 37 references indexed in Scilit:
- The role of superoxide anion generation in phagocytic bactericidal activity. Studies with normal and chronic granulomatous disease leukocytes.Journal of Clinical Investigation, 1975
- The role of pH in the chemiluminescent response of the myeloperoxidase-halide-HOOH antimicrobial systemBiochemical and Biophysical Research Communications, 1975
- Halide dependence of the myeloperoxidase-mediated antimicrobial system of the polymorphonuclear leukocyte in the phenomenon of electronic excitationBiochemical and Biophysical Research Communications, 1975
- The superoxide anion and singlet molecular oxygen: Their role in the microbicidal activity of the polymorphonuclear leukocyteBiochemical and Biophysical Research Communications, 1974
- Is singlet oxygen a substrate for superoxide dismutase? NoFEBS Letters, 1974
- Production of superoxide radical during the decomposition of potassium peroxochromate(V)Biochemistry, 1974
- Singlet molecular oxygen in biological systems: Non-quenching of singlet oxygen-mediated chemiluminescence by superoxide dismutaseBiochemical and Biophysical Research Communications, 1974
- Evidence for the generation of an electronic excitation state(s) in human polymorphonuclear leukocytes and its participation in bactericidal activityBiochemical and Biophysical Research Communications, 1972
- Erythrocuprein and singlet oxygenFEBS Letters, 1972
- The microestimation of succinate and the extinction coefficient of cytochrome cBiochimica et Biophysica Acta, 1959