首页> 外文OA文献 >Involvement of cytosolic phospholipase A2, and the subsequent release of arachidonic acid, in signalling by rac for the generation of intracellular reactive oxygen species in rat-2 fibroblasts.
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Involvement of cytosolic phospholipase A2, and the subsequent release of arachidonic acid, in signalling by rac for the generation of intracellular reactive oxygen species in rat-2 fibroblasts.

机译:胞质磷脂酶A2的参与,以及花生四烯酸的后续释放,通过rac在大鼠2成纤维细胞中产生细胞内活性氧的信号传导中。

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摘要

Although there have been a number of recent studies on the role of Rac in the generation of reactive oxygen species (ROS), details of the signalling pathway remain unclear. In the present study we analysed the extent to which the activation of cytosolic phospholipase A(2) and the resultant release of arachidonic acid (AA) are involved in the Rac-mediated generation of ROS. Transfection of Rat-2 cells with RacV12, a constitutively active form of Rac1, induced elevated levels of ROS, as reflected by increased H(2)O(2)-sensitive fluorescence of 2', 7'-dichlorofluorescein. These effects could be blocked by inhibiting phospholipase A(2) or 5-lipoxygenase but not by inhibiting cyclo-oxygenase. The application of exogenous AA increased levels of ROS but the effect was dependent on the further metabolism of AA to leukotrienes C(4)/D(4)/E(4) by 5-lipoxygenase. Indeed, the exogenous application of a mixture of leukotrienes C(4)/D(4)/E(4) elicited transient elevations in the levels of ROS that were blocked by catalase. These findings indicate that phospholipase A(2) and subsequent AA metabolism by 5-lipoxygenase act as downstream mediators in a Rac signalling pathway leading to the generation of ROS.
机译:尽管最近有许多关于Rac在活性氧(ROS)产生中的作用的研究,但有关信号传导途径的细节仍不清楚。在本研究中,我们分析了胞质磷脂酶A(2)的激活和花生四烯酸(AA)的最终释放与Rac介导的ROS产生的程度。用RacV12(Rac1的组成型活性形式)转染Rat-2细胞诱导水平升高的ROS,如2',7'-dichlorofluorescein的H(2)O(2)敏感荧光增加所反映。这些作用可以通过抑制磷脂酶A(2)或5-脂氧合酶来阻止,但不能通过抑制环氧合酶来阻止。外源AA的应用增加了ROS的水平,但效果取决于5-脂氧合酶将AA进一步代谢为白三烯C(4)/ D(4)/ E(4)。确实,白三烯C(4)/ D(4)/ E(4)混合物的外源应用引起了过氧化氢酶阻断的ROS水平的瞬时升高。这些发现表明磷脂酶A(2)和随后的5-脂氧合酶的AA代谢在Rac信号通路中导致ROS的下游介质。

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