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维生素E上调巨核细胞中花生四烯酸的释放及磷脂酶A2的活性。

Vitamin E up-regulates arachidonic acid release and phospholipase A2 in megakaryocytes.

作者信息

Chan A C, Wagner M, Kennedy C, Chen E, Lanuville O, Mezl V A, Tran K, Choy P C

机构信息

Department of Biochemistry, University of Ottawa, Ontario, Canada.

出版信息

Mol Cell Biochem. 1998 Dec;189(1-2):153-9. doi: 10.1023/a:1006954015678.

Abstract

The release of arachidonic acid is the rate limiting step in eicosanoid synthesis. In mammalian cells, the release of arachidonic acid is catalyzed by several enzymes. The 85 kDa cytosolic phospholipase A2 (cPLA2) is the key enzyme for the release reaction because of its specific acyl selectivity in phospholipid substrates. We have previously reported that vitamin E enrichment potentiates the arachidonic acid release as well as the spontaneous prostacyclin release in human endothelial cells. In contrast, similar enrichment of diets caused a dose-dependent suppression of platelet thromboxane synthesis. Therefore, the present study was undertaken to determine the effect of vitamin E on arachidonate release and phospholipaseA2 activity in a platelet precursor cell, the MEG-01 megakaryocyte cell line. When these cells were incubated with different concentrations of vitamin E, cellular incorporation was linear with the dosages of this vitamin. Determination of arachidonate release after labeling cells with [3H]-arachidonate showed that vitamin E enrichment caused a dose-dependent increase in ionophore A23187-induced [3H]-arachidonic acid release. Analysis of PLA2 activity showed that activity was detected in the cytosol and this activity was completely abolished by the addition of anti-cPLA2, antibody. Determination of cPLA2 activity demonstrated that vitamin E enrichment caused an increase in enzyme activity. Analysis of cPLA2 protein by Western blot revealed that vitamin E caused an increase in enzyme protein. These data showed that the potentiation of arachidonic acid release and cPLA2, activity by vitamin E was mediated by the enhanced expression of cPLA2 protein.

摘要

花生四烯酸的释放是类花生酸合成中的限速步骤。在哺乳动物细胞中,花生四烯酸的释放由几种酶催化。85 kDa的胞质磷脂酶A2(cPLA2)是释放反应的关键酶,因为它在磷脂底物中具有特定的酰基选择性。我们之前报道过,维生素E富集可增强人内皮细胞中花生四烯酸的释放以及自发性前列环素的释放。相比之下,类似的饮食富集导致血小板血栓素合成呈剂量依赖性抑制。因此,本研究旨在确定维生素E对血小板前体细胞MEG-01巨核细胞系中花生四烯酸释放和磷脂酶A2活性的影响。当这些细胞与不同浓度的维生素E孵育时,细胞摄取与该维生素的剂量呈线性关系。用[3H] - 花生四烯酸标记细胞后测定花生四烯酸释放,结果表明维生素E富集导致离子载体A23187诱导的[3H] - 花生四烯酸释放呈剂量依赖性增加。对磷脂酶A2活性的分析表明,在胞质溶胶中检测到活性,并且添加抗cPLA2抗体后该活性完全被消除。对cPLA2活性的测定表明,维生素E富集导致酶活性增加。通过蛋白质印迹法分析cPLA2蛋白表明,维生素E导致酶蛋白增加。这些数据表明,维生素E对花生四烯酸释放和cPLA2活性的增强作用是由cPLA2蛋白表达增强介导的。

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