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在表达重组5-脂氧合酶的U937细胞中白三烯的合成。

Leukotriene synthesis in U937 cells expressing recombinant 5-lipoxygenase.

作者信息

Kargman S, Rousseau P, Reid G K, Rouzer C A, Mancini J A, Rands E, Dixon R A, Diehl R E, Léveillé C, Nathaniel D

机构信息

Department of Pharmacology, Merck Frosst Centre for Therapeutic Research, Pointe Claire-Dorval, Quebec, Canada.

出版信息

J Lipid Mediat. 1993 May;7(1):31-45.

PMID:8358023
Abstract

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.

摘要

人早幼粒细胞系U937不表达5-脂氧合酶,但表达5-脂氧合酶激活蛋白(FLAP)。U937细胞在钙离子载体A23187刺激后不合成白三烯。U937细胞经二甲基亚砜(DMSO)诱导向更成熟的单核细胞-巨噬细胞谱系分化后,FLAP表达上调,但5-脂氧合酶不表达。这些经DMSO分化的U937细胞也缺乏合成白三烯的能力。我们使用逆转录病毒载体将编码5-脂氧合酶的病毒RNA导入U937细胞,并检测了这些细胞在A23187刺激后5-脂氧合酶、FLAP、白三烯和5-羟基二十碳四烯酸(5-HETE)的合成情况。感染了5-脂氧合酶RNA的未分化U937细胞表达5-脂氧合酶和FLAP,但在这些细胞经A23187刺激后未检测到白三烯和5-HETE。将感染了5-脂氧合酶的U937细胞暴露于DMSO可增加5-脂氧合酶和FLAP的表达,并且这些细胞在A23187刺激下产生白三烯和5-HETE。这些产物的合成受到MK-886的抑制,MK-886是一种与FLAP特异性结合的化合物。

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