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Generation of superoxide anion and chemiluminescence by human monocytes during phagocytosis and on contact with surface-bound immunoglobulin G.

R B Johnston, +2 more
- 01 Jun 1976 - 
- Vol. 143, Iss: 6, pp 1551-1556
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TLDR
Oxygen metabolites released from mononuclear phagocytes are highly reactive and could play a part in both the beneficial and detrimental aspects of chronic inflammation.
Abstract
Extent of O-2-release and chemiluminescence, attributed to singlet oxygen, has been compared in human monocytes and neutrophils during phagocytosis, stimulation by the surface-active agent phorbol myristate acetate, or contact with aggregated IgG in a model of immune complex disease. Monocytes generated O-2-and chemiluminescence with each of the three stimuli, although values were significantly less than those of neutrophils from the same individuals. Lymphocytes had no significant activity in either assay with any stimulus. Oxygen metabolites released from mononuclear phagocytes are highly reactive and could play a part in both the beneficial and detrimental aspects of chronic inflammation.

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Production of Large Amounts of Hydrogen Peroxide by Human Tumor Cells

TL;DR: Constitutive generation of large amounts of reactive oxygen intermediates, if it occurs in vivo, might contribute to the ability of some tumors to mutate, inhibit antiproteases, injure local tissues, and therefore promote tumor heterogeneity, invasion, and metastasis.
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Increased superoxide anion production by immunologically activated and chemically elicited macrophages.

TL;DR: It is concluded that the phagocytosis- associated respiratory burst is significantly enhanced in mononuclear phagocytes obtained ai~r chemical inflammation or BCG infection.
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Receptors for C3b and C3bi promote phagocytosis but not the release of toxic oxygen from human phagocytes

TL;DR: The C3b and C3bi receptors of monocytes and granulocytes do not signal the generation of toxic oxygen intermediates from these cells, and release of H2O2 is measured during spreading on ligand-coated culture surfaces.
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Extracellular cytolysis by activated macrophages and granulocytes. II. Hydrogen peroxide as a mediator of cytotoxicity.

TL;DR: It is demonstrated that release of H2O2 was both necessary and sufficient for cytolysis by BCG-activated macrophages and by granulocytes when pharmacologically triggered, and that lactoperoxidase may have diverted H 2O2 from the oxidation of target cells to oxidation of substances in serum.
References
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Journal ArticleDOI

Biological defense mechanisms. The production by leukocytes of superoxide, a potential bactericidal agent.

TL;DR: O(2) (-) is made by leukocytes under circumstances which suggest that it may be involved in bacterial killing, and is identified as the agent responsible for the leukocyte-mediated reduction of cytochrome c.
Book

Free radical mechanisms in tissue injury

TL;DR: This short review of free radicals discusses certain types of free radical, such as nitroxyl-radicals and free radicals stabilized by steric or derealization features, which are stable enough to be crystallised and stored at temperatures above 0°.
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Evidence for the generation of an electronic excitation state(s) in human polymorphonuclear leukocytes and its participation in bactericidal activity

TL;DR: It is proposed that the CL of PMN reflects the generation of singlet oxygen, 1 0 2 , which acts per , se , as the bactericidal and/or CL species.
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The role of superoxide anion generation in phagocytic bactericidal activity. Studies with normal and chronic granulomatous disease leukocytes.

TL;DR: It would seem clear from these and other studies that the granulo cyte elaborates O2- as a concomitant of the respiratory burst that occurs with phagocytosis, and a requirement for .OH in thephagocytic bactericidal event might explain the apparent requirement for both O1- and H2O2 for such activity.
Journal ArticleDOI

Antimicrobial mechanisms in neutrophilic polymorphonuclear leukocytes.

TL;DR: Particular organisms are susceptible to more than one antimicrobial system and thus may be effectively handled by back-up systems when one is absent, and an organism normally killed by the peroxidase system may be handled less efficiently but adequately when MPO is absent by other oxygen-dependent antimicrobial systems.
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