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Usage Information

Superoxide Production by Digitonin-Stimulated Guinea Pig Granulocytes: THE EFFECTS OF N-ETHYL MALEIMIDE, DIVALENT CATIONS, AND GLYCOLYTIC AND MITOCHONDRIAL INHIBITORS ON THE ACTIVATION OF THE SUPEROXIDE GENERATING SYSTEM
Harvey J. Cohen, Margaret E. Chovaniec
Harvey J. Cohen, Margaret E. Chovaniec
Published April 1, 1978
Citation Information: J Clin Invest. 1978;61(4):1088-1096. https://doi.org/10.1172/JCI109008.
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Superoxide Production by Digitonin-Stimulated Guinea Pig Granulocytes: THE EFFECTS OF N-ETHYL MALEIMIDE, DIVALENT CATIONS, AND GLYCOLYTIC AND MITOCHONDRIAL INHIBITORS ON THE ACTIVATION OF THE SUPEROXIDE GENERATING SYSTEM

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Abstract

N-ethylmaleimide, divalent cations, ethylene glycol bis (β aminoethyl ether) N,N,N′,N′,-tetraacetate, 2-deoxyglucose, cyanide, and dinitrophenol were examined for their effect on the ability of guinea pig granulocytes to generate superoxide (O2−) when stimulated by digitonin. N-ethylmaleimide (1 mM) inhibits only when added before complete activation of the O2− generating system, and at lower concentrations (0.05-0.2 mM) slows the activation process. Ca++ is required for maximum O2− generation, and Mg++ decreases the amount of Ca++ required. Ethylene glycol bis (β aminoethyl ether) N,N,N′,N′,-tetraacetate (10 mM) inhibits only if added before complete activation. Incubation of cells in 2-DOG causes a time- and concentration-dependent inhibition of O2− generation. It also increases the time required for activation of this system. Cyanide and dinitrophenol increase the rate of O2− production. However, when these compounds are added to cells whose O2− production is partially inhibited by incubation in 2-deoxyglucose, complete inhibition results. If cyanide or dinitrophenol is added after activation of 2-deoxyglucose-treated cells, no further inhibition occurs. On the basis of the above results, we conclude that the activation of the O2− generating system is N-ethylmaleimide sensitive, Ca++ dependent, and energy requiring, but that the activity of the enzyme system in the cell is not.

Authors

Harvey J. Cohen, Margaret E. Chovaniec

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