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Calcium-independent phospholipase A(2) mediates proliferation of human promonocytic U937 cells

机译:钙非依赖性磷脂酶A(2)介导人类单核U937细胞的增殖

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摘要

We have investigated the possible involvement of two intracellular phospholipases A(2), namely group VIA calcium-independent phospholipase A(2) (iPLA(2)-VIA) and group IVA cytosolic phospholipase A(2) (cPLA(2)alpha), in the regulation of human promonocytic U937 cell proliferation. Inhibition of iPLA(2)-VIA activity by either pharmacological inhibitors such as bromoenol lactone or methyl arachidonyl fluorophosphonate or using specific antisense technology strongly blunted U937 cell proliferation. In contrast, inhibition of cPLA(2)alpha had no significant effect on U937 proliferation. Evaluation of iPLA(2)-VIA activity in cell cycle-synchronized cells revealed highest activity at G(2)/M and late S phases, and lowest at G(1). Phosphatidylcholine levels showed the opposite trend, peaking at G(1) and lowest at G(2)/M and late S phase. Reduction of U937 cell proliferation by inhibition of iPLA(2)-VIA activity was associated with arrest in G(2)/M and S phases. The iPLA(2)-VIA effects were found to be independent of the generation of free arachidonic acid or one of its oxygenated metabolites, and may work through regulation of the cellular level of phosphatidylcholine, a structural lipid that is required for cell growth/membrane expansion.
机译:我们已经调查了两个胞内磷脂酶A(2)的可能参与,即VIA组钙独立磷脂酶A(2)(iPLA(2)-VIA)和IVA胞质磷脂酶A(2)(cPLA(2)alpha) ,在人类单核细胞U937细胞增殖的调节中。 iPLA(2)-VIA活性的抑制是通过药理学抑制剂如溴烯醇内酯或甲基花生四烯酸氟膦酸酯或使用特定的反义技术可大大削弱U937细胞的增殖。相反,对cPLA(2)alpha的抑制对U937的增殖没有明显的影响。对细胞周期同步细胞中iPLA(2)-VIA活性的评估显示,在G(2)/ M和晚期S期的活性最高,而在G(1)的活性最低。磷脂酰胆碱水平显示出相反的趋势,在G(1)达到峰值,在G(2)/ M和后期S期最低。通过抑制iPLA(2)-VIA活性来减少U937细胞增殖与G(2)/ M和S期逮捕有关。发现iPLA(2)-VIA的作用与游离花生四烯酸或其氧化代谢产物的产生无关,并且可能通过调节磷脂酰胆碱(一种细胞生长/膜所需的结构脂质)的细胞水平起作用扩张。

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