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Thymocyte cyclic AMP and cyclic GMP response to treatment with metabolites issued from the lipoxygenase pathway.
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1985
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Lipid PeroxidationImmature Pna+Immune RegulationImmunologyImmunologic MechanismCgmp ProductionCellular PhysiologyOxidative StressInflammationLipoxygenase PathwayBiochemistryAutoimmunityImmune FunctionMetabolomicsPharmacologyCell BiologyCgmp LevelsPhysiologyThymocyte Cyclic AmpCyclic Gmp ResponseThyroid HormoneMetabolismMedicineCellular Immune ResponseCarbonyl Metabolism
Evidence has been presented that cGMP is the second messenger for the lipoxygenase metabolites 15-HETE and LTB4 in the mouse splenocyte and thymocyte. Incubation of splenocytes with 10(-7) to 10(-9) M 15-HETE caused a slight decrease in cAMP levels and an increase in cGMP levels after 10 to 20 min. Mature PNA-, immature PNA+, and whole thymocytes treated with 10(-7) to 10(-10) M 15-HETE and 10(-11) M LTB4 showed an approximately 100% increase in cGMP production. In mixed lymphocyte reactions, 15-HETE- and LTB4-treated PNA+, PNA-, and whole thymocyte populations inhibited thymidine uptake by fresh allostimulated splenocytes. These results demonstrate that the eicosanoid-induced generation of suppressor cells follows a rise in lymphocyte cGMP levels.