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含油酸的二酰甘油通过人T细胞中的TRPC3/6通道诱导细胞内钙离子浓度([Ca(2+)](i))升高。

Diacylglycerol-containing oleic acid induces increases in [Ca(2+)](i) via TRPC3/6 channels in human T-cells.

作者信息

Carrillo Celia, Hichami Aziz, Andreoletti Pierre, Cherkaoui-Malki Mustapha, del Mar Cavia María, Abdoul-Azize Souleymane, Alonso-Torre Sara R, Khan Naim Akhtar

机构信息

Área de Nutrición y Bromatología, Facultad de Ciencias, Universidad de Burgos, Pl. Misael Bañuelos s/n, 09001 Burgos, Spain.

出版信息

Biochim Biophys Acta. 2012 Apr;1821(4):618-26. doi: 10.1016/j.bbalip.2012.01.008. Epub 2012 Jan 25.

Abstract

Though most of the studies have focused on the effects of free fatty acids on T-cell activation, fatty acids incorporated into plasma membrane phospholipids may also affect cell signaling via diacylglycerol (DAG), generally produced by phospholipid hydrolysis. In the present study, we have synthesized a DAG-containing oleic acid and studied its implication in the modulation of calcium signaling in human Jurkat T-cells. 1-palmitoyl-2-oleoyl-sn-glycerol (POG) induced a dose-dependent increase in Ca(2+). This effect was due to the presence of oleic acid at the sn-2 position as no differences were observed between POG and 1-stearoly-2-oleoyl-sn-glycerol (SOG). However, the substitution of oleic acid with arachidonic acid at the sn-2 position of the DAG moiety exerted a different response on the increases in Ca(2+) in these cells. POG-evoked increases in Ca(2+) were not due to its metabolites. Furthermore, POG-induced increases in Ca(2+) were due to the opening of TRPC3/TRPC6 channels as silencing of TRPC3 and TRPC6 genes by shRNA abolished calcium entry. Moreover, disruption of lipid rafts with methyl-β-cyclodextrin completely abolished POG-evoked increases in Ca(2+). In conclusion, our results demonstrate that oleic acid can influence T-lymphocyte functions, in the conjugated form of DAG, via opening TRPC3/6 channels.

摘要

尽管大多数研究都集中在游离脂肪酸对T细胞活化的影响上,但掺入质膜磷脂中的脂肪酸也可能通过通常由磷脂水解产生的二酰基甘油(DAG)影响细胞信号传导。在本研究中,我们合成了一种含DAG的油酸,并研究了其在调节人Jurkat T细胞钙信号传导中的作用。1-棕榈酰-2-油酰-sn-甘油(POG)诱导Ca(2+)呈剂量依赖性增加。这种效应是由于sn-2位存在油酸,因为在POG和1-硬脂酰-2-油酰-sn-甘油(SOG)之间未观察到差异。然而,在DAG部分的sn-2位用花生四烯酸取代油酸对这些细胞中Ca(2+)的增加产生了不同的反应。POG引起的Ca(2+)增加不是由于其代谢产物。此外,POG诱导的Ca(2+)增加是由于TRPC3/TRPC6通道的开放,因为通过shRNA沉默TRPC3和TRPC6基因消除了钙内流。此外,用甲基-β-环糊精破坏脂筏完全消除了POG引起的Ca(2+)增加。总之,我们的结果表明,油酸可以通过打开TRPC3/6通道,以DAG的共轭形式影响T淋巴细胞功能。

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