Hirata K, Maghni K, Borgeat P, Sirois P
Department of Pharmacology, Faculty of Medicine, University of Sherbrooke, PQ, Canada.
J Immunol. 1990 Mar 1;144(5):1880-5.
The metabolism of arachidonic acid (AA) was investigated in purified guinea pig alveolar eosinophils and macrophages. Alveolar eosinophils produced 12S-hydroxy-5,8,10-heptadecatraenoic acid (HHT) and small amounts only of 5-lipoxygenase products when stimulated by AA (10 microM) or ionophore A23187 (2 microM). However, when the cell suspensions were stimulated with both AA and A23187, the cells produced HHT, leukotriene (LT) B4, and 5S-hydroxy-6,8,11,14-eicosatetraenoic acid, whereas LTC4, D4, and E4 were undetectable. Similarly, alveolar macrophages stimulated with A23187 produced HHT, 5-hydroxy-6,8,11,14-eicosatetraenoic acid, and LTB4 but no peptido-leukotrienes. When LTA4 was added to suspensions of eosinophils and macrophages, only LTB4 was formed, whereas in parallel experiments, intact human platelets incubated with LTA4 produced LTC4. These data suggest that guinea pig alveolar eosinophils and macrophages contain both cyclooxygenase and 5-lipoxygenase, but do not produce peptido-leukotrienes, probably lacking LTA4 glutathione transferase activity. These studies demonstrate that guinea pig eosinophils differ from eosinophils of other animal species which have been shown to be major sources of leukotriene C4. The present data imply that eosinophils and macrophages are not the source of peptido-leukotrienes in anaphylactic guinea pig lungs.
在纯化的豚鼠肺泡嗜酸性粒细胞和巨噬细胞中研究了花生四烯酸(AA)的代谢。当受到AA(10微摩尔)或离子载体A23187(2微摩尔)刺激时,肺泡嗜酸性粒细胞产生12S-羟基-5,8,10-十七碳三烯酸(HHT),仅产生少量的5-脂氧合酶产物。然而,当细胞悬液同时受到AA和A23187刺激时,细胞产生HHT、白三烯(LT)B4和5S-羟基-6,8,11,14-二十碳四烯酸,而LTC4、D4和E4未检测到。同样,用A23187刺激的肺泡巨噬细胞产生HHT、5-羟基-6,8,11,14-二十碳四烯酸和LTB4,但不产生肽白三烯。当将LTA4添加到嗜酸性粒细胞和巨噬细胞悬液中时,仅形成LTB4,而在平行实验中,与LTA4一起孵育的完整人血小板产生LTC4。这些数据表明,豚鼠肺泡嗜酸性粒细胞和巨噬细胞同时含有环氧化酶和5-脂氧合酶,但不产生肽白三烯,可能缺乏LTA4谷胱甘肽转移酶活性。这些研究表明,豚鼠嗜酸性粒细胞不同于其他动物物种的嗜酸性粒细胞,后者已被证明是白三烯C4的主要来源。目前的数据表明,嗜酸性粒细胞和巨噬细胞不是过敏性豚鼠肺中肽白三烯的来源。
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