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Enhancement of mononuclear procoagulant activity by platelet 12-hydroxyeicosatetraenoic acid.

机译:血小板12-羟基二十碳四烯酸增强单核促凝活性。

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摘要

Platelets induce generation of procoagulant tissue factor activity (TFa) by mononuclear leukocytes, and also enhance the TFa induced by endotoxin. Our present investigation demonstrated that arachidonic acid, which by itself had no effect on mononuclear TFa, greatly enhanced platelet-induced TFa. The effect was concentration dependent for both platelets and arachidonate (1-20 microM); other fatty acids tested were inactive. The enhancing effect of arachidonate was more pronounced if platelets were exposed to aspirin, suggesting lipoxygenase product involvement. Production of 12-hydroxyeicosatetraenoic acid (12-HETE) was demonstrated biochemically in aspirin-treated platelet/arachidonate/mononuclear cell preparations that generated high levels of TFa. The enhancing role of 12-HETE was verified as follows. Addition of platelet-derived or synthetic 12-HETE amplified endotoxin-induced TFa more than threefold. Other lipoxygenase products were inactive. Enhancement of mononuclear cell TFa by 12-HETE represents a newly described biological function for this eicosanoid in cell-cell interactions between platelets and mononuclear cells.
机译:血小板诱导单核白细胞产生促凝血组织因子活性(TFa),并且还增强内毒素诱导的TFa。我们目前的研究表明,花生四烯酸本身对单核TFa没有影响,但大大增强了血小板诱导的TFa。对于血小板和花生四烯酸盐(1-20 microM),效果均与浓度有关。测试的其他脂肪酸没有活性。如果血小板暴露于阿司匹林,花生四烯酸的增强作用更加明显,表明脂氧合酶产物参与其中。在产生高水平TFa的阿司匹林处理的血小板/花生四烯酸/单核细胞制剂中,通过化学方法证明了12-羟基二十碳四烯酸(12-HETE)的产生。如下证实了12-HETE的增强作用。加入血小板衍生的或合成的12-HETE扩增的内毒素诱导的TFa超过三倍。其他脂氧合酶产物无活性。 12-HETE增强单核细胞TFa代表了该类花生酸在血小板和单核细胞之间的细胞相互作用中的新描述的生物学功能。

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