Powell W S, Chung D, Gravel S
Meakins-Christie Laboratories, Department of Medicine, McGill University, Montreal, Quebec, Canada.
J Immunol. 1995 Apr 15;154(8):4123-32.
Human neutrophils and monocytes contain a highly specific dehydrogenase which converts 5-hydroxy-6,8,11,14-eicosatetraenoic acid (5-HETE) to 5-oxo-6,8,11,14-eicosatetraenoic acid (5-oxo-ETE). We have previously shown that 5-oxo-ETE is a potent stimulus of neutrophil calcium levels and migration and have now investigated its effects on human eosinophils. 5-Oxo-ETE is a potent stimulus of eosinophil migration, with significant effects being detected at concentrations as low as 1 nM and a maximal response at 1 microM. The responses elicited by 5-oxo-ETE were about two to three times greater than those to platelet-activating factor (PAF) and 5-oxo-15-hydroxy-6,8,11,13-eicosatetraenoic acid (5-oxo-15-hydroxy-ETE) at all concentrations tested between 10 nM and 1 microM. Leukotrienes B4 and D4 also significantly stimulated eosinophil migration, but the maximal responses to these agonists were only about 4% of the maximal response to 5-oxo-ETE. A low concentration of 5-oxo-ETE (1 nM) potentiated eosinophil migration in response to PAF. Eosinophils were capable of converting 5-HETE to 5-oxo-ETE, and this reaction was enhanced by phorbol myristate acetate. Stimulation of eosinophils with A23187 in the presence of low concentrations of arachidonic acid and phorbol 12-myristate 13-acetate led to the formation of 5-oxo-ETE and 5-oxo-15-hydroxy-ETE, but the amounts were considerably less than those of other eicosanoids such as leukotriene C4, cysteine-containing lipoxins, and 5,15-dihydroxy-6E,8Z,11Z,13E-eicosatetraenoic acid. In summary, of all the lipid mediators tested, 5-oxo-ETE was the most effective in stimulating migration of human eosinophils. Although eosinophils are capable of synthesizing 5-oxo-eicosanoids, the amounts detected were relatively small, and other leukocytes such as neutrophils, monocytes, or macrophages may be more important sites for the synthesis of this compound.
人类中性粒细胞和单核细胞含有一种高度特异性的脱氢酶,该酶可将5-羟基-6,8,11,14-二十碳四烯酸(5-HETE)转化为5-氧代-6,8,11,14-二十碳四烯酸(5-氧代-ETE)。我们之前已经表明,5-氧代-ETE是中性粒细胞钙水平和迁移的有效刺激物,现在我们研究了其对人类嗜酸性粒细胞的影响。5-氧代-ETE是嗜酸性粒细胞迁移的有效刺激物,在低至1 nM的浓度下即可检测到显著作用,在1 μM时达到最大反应。在10 nM至1 μM之间的所有测试浓度下,5-氧代-ETE引发的反应比血小板活化因子(PAF)和5-氧代-15-羟基-6,8,11,13-二十碳四烯酸(5-氧代-15-羟基-ETE)引发的反应大约大两到三倍。白三烯B4和D4也显著刺激嗜酸性粒细胞迁移,但对这些激动剂的最大反应仅约为对5-氧代-ETE最大反应的4%。低浓度的5-氧代-ETE(1 nM)可增强嗜酸性粒细胞对PAF的迁移反应。嗜酸性粒细胞能够将5-HETE转化为5-氧代-ETE,并且该反应可被佛波酯肉豆蔻酸酯乙酸盐增强。在低浓度花生四烯酸和佛波醇12-肉豆蔻酸酯13-乙酸盐存在下,用A23187刺激嗜酸性粒细胞会导致5-氧代-ETE和5-氧代-15-羟基-ETE的形成,但生成量远低于其他类花生酸,如白三烯C4、含半胱氨酸的脂氧素和5,15-二羟基-6E,8Z,11Z,13E-二十碳四烯酸。总之,在所有测试的脂质介质中,5-氧代-ETE在刺激人类嗜酸性粒细胞迁移方面最有效。虽然嗜酸性粒细胞能够合成5-氧代类花生酸,但检测到的量相对较小,其他白细胞如中性粒细胞、单核细胞或巨噬细胞可能是该化合物合成的更重要部位。