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PMID: 6594417 Published · ppublish English Journal Article

Activation of a NADPH oxidase from horse polymorphonuclear leukocytes in a cell-free system.

Journal of leukocyte biology ·Vol. 36 ·No. 6 ·1984-12-00 ·Pages 751-9

Heyneman RA, Vercauteren RE

Abstract

A postnuclear cell fraction from resting horse polymorphonuclear (PMN) leukocytes incubated with fatty acid-salt ions such as oleate or linoleate generated a NADPH-dependent oxygen consumption and superoxide production. Oxidative activity was negligible or absent in the postnuclear fraction from mononuclear leukocytes, p-chloromercuribenzene sulfonic acid-treated granulocytes, and granulocytes from a patient with chronic granulomatous disease. Although consistently associated with the membrane fraction from resting PMN leukocytes, the superoxide-generating activity was shown to be dependent on a thus far unknown cytosolic constituent. The apparent Km's for NADPH and NADH (66 and 1,600 microM, respectively), the pH optimum for the reaction (7.0), the cyanide insensitivity, and transient nature of the reaction together with the stoichiometric relationship between oxygen uptake and NADPH oxidation led to the conclusion that in the presence of cytosol a cell-free latent respiratory burst oxidase can be converted into an active enzyme by interaction with oleate micelles.

MeSH Terms
Animals Enzyme Activation Horses Hydrogen-Ion Concentration Kinetics Leukapheresis NADH, NADPH Oxidoreductases/blood NADPH Oxidases Neutrophils/cytology,enzymology,metabolism Oxygen Consumption Subcellular Fractions/enzymology
Chemicals
NADH, NADPH Oxidoreductases NADPH Oxidases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Heyneman R A
Vercauteren R E
Article Info
Journal
Journal of leukocyte biology
Abbr.
J Leukoc Biol
ISSN
0741-5400
Published
1984-12-00
Pages
751-9
Language
English
Region
United States
NLM ID
8405628
Subset
IM
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