表达重组5-脂氧合酶的U937细胞合成白三烯

Journal of lipid mediators Pub Date : 1993-05-01
S Kargman, P Rousseau, G K Reid, C A Rouzer, J A Mancini, E Rands, R A Dixon, R E Diehl, C Léveillé, D Nathaniel
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引用次数: 0

摘要

U937人早幼粒细胞细胞系不表达5-脂氧合酶,但表达5-脂氧合酶激活蛋白(FLAP)。U937细胞受钙离子载体A23187刺激后不合成白三烯。二甲基亚砜(DMSO)将U937细胞分化为更成熟的单核-巨噬细胞谱系,诱导FLAP表达,但不诱导5-脂氧合酶的表达。这些dmso分化的U937细胞也缺乏合成白三烯的能力。我们用逆转录病毒载体将编码5-脂氧合酶的病毒RNA感染到U937细胞中,用A23187刺激这些细胞后,检测了5-脂氧合酶、FLAP、白三烯和5-羟基二碳四烯酸(5-HETE)的合成。未分化的U937细胞感染5-脂氧合酶RNA后表达5-脂氧合酶和FLAP,但A23187刺激后未检测到白三烯和5-HETE。5-脂氧合酶感染的U937细胞暴露于DMSO后,5-脂氧合酶和FLAP的表达增加,这些细胞对A23187产生白三烯和5-HETE。这些产物的合成受到MK-886的抑制,MK-886是一种特异性结合FLAP的化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Leukotriene synthesis in U937 cells expressing recombinant 5-lipoxygenase.

The U937 human promyelocytic cell line does not express 5-lipoxygenase, but does express 5-lipoxygenase-activating protein (FLAP). U937 cells do not synthesize leukotrienes after stimulation by calcium ionophore A23187. Dimethyl sulfoxide (DMSO) differentiation of U937 cells, towards a more mature monocyte-macrophage lineage, induces the expression of FLAP but not 5-lipoxygenase. These DMSO-differentiated U937 cells also lack the ability to synthesize leukotrienes. We infected viral RNA coding for 5-lipoxygenase into U937 cells using a retroviral vector and measured the synthesis of 5-lipoxygenase, FLAP, leukotrienes and 5-hydroxyeicosatetraenoic acid (5-HETE) by these cells after stimulation with A23187. Undifferentiated U937 cells infected with 5-lipoxygenase RNA expressed 5-lipoxygenase and FLAP but neither leukotrienes nor 5-HETE were detected after these cells were stimulated with A23187. Exposure of the 5-lipoxygenase-infected U937 cells to DMSO increased the expression of 5-lipoxygenase and FLAP, and these cells produced leukotrienes and 5-HETE in response to A23187. The synthesis of these products was inhibited by MK-886, a compound which specifically binds to FLAP.

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