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Transcriptional effects of phospholipid fatty acid profile on rainbow trout liver cells exposed to methylmercury

机译:磷脂脂肪酸谱对甲基汞暴露于褐鳟肝细胞的转录作用

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Lipids, and their constitutive fatty acids, are key nutrients for fish health as they provide energy, maintain cell structure, are precursors of signalling molecules and act as nuclear receptor ligands. These specific roles may be of crucial importance in a context of exposure to pollutants. We recently showed that the fatty acid profile of rainbow trout liver cell phospholipids modulates sensitivity to an acute methylmercury challenge. In order to investigate mechanisms of effects, we herein tested whether specific polyunsaturated fatty acids (PUFAs) may protect cells from methylmercury through decreasing intracellular mercury accumulation and/or enhancing cellular defences (e.g. via modulation of gene expression patterns). We also investigated the inverse relationship and assessed the impact of methylmercury on cellular fatty acid metabolism. To do so, the fatty acid composition of rainbow trout liver cell phospholipids was first modified by incubating them in a medium enriched in a specific PUFA from either the n-3 family (alpha-linolenic acid, ALA; eicosapentaenoic acid, EPA) or the n-6 family (linoleic acid, LA; arachidonic acid, AA). Cells were then exposed to methylmercury (0.15 or 0.50 mu M) for 24 h and sampled thereafter for assessing phospholipid fatty acid profile, intracellular total mercury burden, and expression pattern of genes involved in fatty acid metabolism, synthesis of PUFA-derived signalling molecules and stress response. We observed that cells incorporated the given PUFA and some biotransformation products in their phospholipids. Methylmercury had few impacts on this cellular phospholipid composition. None of the PUFA enrichments affected the cellular mercury burden, suggesting that the previously observed cytoprotection conferred by ALA and EPA was not linked to a global decrease in cellular accumulation of mercury. Fatty acid enrichments and methylmercury exposure both modulated gene expression patterns. Genes involved in the synthesis of PUFA-derived signalling molecules, in stress response and the orphan cytochrome P450 20A1 were identified as possible sites of interaction between fatty acids and methylmercury in rainbow trout liver cells.
机译:脂质和它们的组成型脂肪酸是用于鱼类健康的关键营养素,因为它们提供能量,维持细胞结构,是信号分子的前体,并作为核受体配体。这些特定的角色在暴露于污染物的背景下可能是至关重要的。我们最近表明,虹鳟鱼肝细胞磷脂的脂肪酸谱调节对急性甲基汞攻击的敏感性。为了调查效果的机制,我们在本文中测试了特定的多不饱和脂肪酸(PUFA)是否可以通过降低细胞内汞积累和/或增强细胞防御(例如,通过基因表达模式的调节来保护细胞免受甲基汞的影响。我们还研究了反相关系并评估了甲基汞对细胞脂肪酸代谢的影响。为此,首先通过将它们孵育在富含N-3家族(α-亚麻酸,ALA; eicosapentaeno酸,EPA)或eICosapentaeno酸,EPA)或者中,首先通过将它们的培养基中培养至富含富含PUFA的培养基来修饰脂肪酸组合物。 N-6系列(亚油酸,LA; arachidonic acid,AA)。然后将细胞暴露于甲基汞(0.15或0.50μm)24小时并此后进行取样,用于评估磷脂脂肪酸谱,细胞内汞负担和参与脂肪酸代谢的基因的表达模式,合成PUFA衍生的信号分子和压力反应。我们观察到细胞在其磷脂中掺入了给定的PUFA和一些生物转化产物。甲基汞对这种细胞磷脂组合物的影响很少。普华植物浓缩都影响了细胞汞负担,这表明以前观察到的ALA和EPA的细胞保护与汞的细胞积累的全局降低没有与汞的累加的降低相关联。脂肪酸富集和甲基汞曝光都是调节基因表达模式。参与合成PUFA衍生的信号分子的基因,应力反应和孤儿细胞色素P450 20A1被鉴定为诸如虹鳟鱼肝细胞中脂肪酸和甲基汞之间的相互作用的可能性。

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