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Research Article Free access | 10.1172/JCI113377
Department of Internal Medicine, Faculty of Medicine, Kyoto University, Japan.
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Department of Internal Medicine, Faculty of Medicine, Kyoto University, Japan.
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Department of Internal Medicine, Faculty of Medicine, Kyoto University, Japan.
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Department of Internal Medicine, Faculty of Medicine, Kyoto University, Japan.
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Department of Internal Medicine, Faculty of Medicine, Kyoto University, Japan.
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Department of Internal Medicine, Faculty of Medicine, Kyoto University, Japan.
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Published March 1, 1988 - More info
Changes in arachidonate metabolism were examined in mouse peritoneal macrophages incubated with various types of lipoproteins. Oxidized low density lipoprotein (LDL) was incorporated by macrophages and stimulated macrophage prostaglandin E2 (PGE2) and leukotriene C4 syntheses, respectively, 10.8- and 10.7-fold higher than by the control. Production of 6-keto-PGF1 alpha, a stable metabolite of prostacyclin, was also stimulated. No stimulation was found with native LDL, which was minimally incorporated by the cells. Acetylated LDL and beta-migrating very low density lipoprotein (beta-VLDL), though incorporated more efficiently than oxidized LDL, also had no stimulatory effect. When oxidized LDL was separated into the lipoprotein-lipid peroxide complex and free lipid peroxides, most of the stimulatory activity was found in the former fraction, indicating that stimulation of arachidonate metabolism in the cell is associated with uptake of the lipoprotein-lipid peroxide complex. These results suggest that peroxidative modification of LDL could contribute to the progression of atheroma by stimulating arachidonate metabolism during incorporation into macrophages.
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