The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Chemiluminescence and superoxide production by myeloperoxidase-deficient leukocytes.
Open accessAbstract
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.
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Cites
Physical and chemical properties of singlet molecular oxygen
Kearns, D. R. (1971) · Chemical Reviews · doi:10.1021/cr60272a004 · Cited by 913
Cited by
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KLEBANOFF, S. J. (1980) · Annals of Internal Medicine · doi:10.7326/0003-4819-93-3-480 · Cited by 868
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Nauseef, W. M. (2007) · Immunological Reviews · doi:10.1111/j.1600-065x.2007.00550.x · Cited by 756
Heyworth, P. G., Cross, A. R., & Curnutte, J. T. (2003) · Current Opinion in Immunology · doi:10.1016/s0952-7915(03)00109-2 · Cited by 396
Ulfig, A., & Leichert, L. I. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03591-y · Cited by 239
Detection of superoxide anion and hydrogen peroxide production by cellular NADPH oxidases
Nauseef, W. M. (2014) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2013.04.040 · Cited by 180
Metadata
- Authors
- Rosen, H., & Klebanoff, S. J.
- Venue
- Journal of Clinical Investigation
- Published
- 1976-07-01
- Volume
- 58
- Issue
- 1
- Pages
- 50-60
- ISSN
- 0021-9738 (ISSN-L)
- OpenAlex
- W2113015414
- Cited by
- 368
- References
- 1
- FWCI
- 9.70
- Type
- journal article
- Language
- en
- Open access
- bronze
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- Rosen, H., & Klebanoff, S. J. (1976). Chemiluminescence and superoxide production by myeloperoxidase-deficient leukocytes. Journal of Clinical Investigation. https://doi.org/10.1172/jci108458
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