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铜诱导贻贝(贻贝)血细胞的免疫调节。

Copper-induced immunomodulation in mussel (Perna canaliculus) haemocytes.

机构信息

Aquaculture Biotechnology Research Group, School of Science, Faculty of Health and Environmental Sciences, Auckland University of Technology, Private Bag 92006, Auckland 1142, New Zealand.

出版信息

Metallomics. 2018 Jul 18;10(7):965-978. doi: 10.1039/c8mt00092a.

Abstract

Copper is a common contaminant in aquatic environments, which may cause physiological dysfunction in marine organisms. However, the toxicity mechanisms of copper in marine bivalves is not fully understood. In this study, we applied an integrated approach that combines flow cytometry and Gas Chromatography-Mass Spectrometry (GC-MS)-based metabolomics to characterize cellular and molecular mechanisms of copper immunotoxicity in New Zealand Greenshell™ mussel (Perna canaliculus) haemolymph. Flow cytometric results showed significant increases in haemocyte mortality, production of reactive oxygen species and apoptosis (via alteration of caspase 3/7 and mitochondrial membrane potential) of haemocytes exposed to increasing total concentrations of Cu2+ (62.5, 125.0 and 187.5 μM) compared to a low Cu2+ concentration (25.0 μM) and control (0.0 μM). In addition to flow cytometric data, our metabolomics results showed alterations of 25 metabolites within the metabolite profile of Cu2+-exposed haemolymph (125 μM) compared to those of control samples. Changes in levels of these metabolites may be considered important signatures of oxidative stress (e.g., glutathione) and apoptosis processes (e.g., alanine, glutamic acid). This study provides insights into the cellular and molecular mechanisms of oxidative stress and apoptosis in marine bivalves and highlights the applicability and reliability of metabolomic techniques for immunotoxicological studies in marine organisms.

摘要

铜是水生环境中的一种常见污染物,可能会导致海洋生物生理功能障碍。然而,铜对海洋双壳贝类的毒性机制尚未完全了解。在这项研究中,我们采用了一种综合方法,结合流式细胞术和基于气相色谱-质谱(GC-MS)的代谢组学,来描述新西兰绿贻贝(Perna canaliculus)血淋巴中铜免疫毒性的细胞和分子机制。流式细胞术结果表明,与低铜浓度(25.0 μM)和对照(0.0 μM)相比,暴露于总铜浓度(62.5、125.0 和 187.5 μM)下的血细胞死亡率、活性氧产生和细胞凋亡(通过改变 caspase 3/7 和线粒体膜电位)显著增加。此外,我们的代谢组学结果表明,与对照样品相比,暴露于铜(125 μM)的血淋巴代谢物图谱中的 25 种代谢物发生了变化。这些代谢物水平的变化可被视为氧化应激(如谷胱甘肽)和细胞凋亡过程(如丙氨酸、谷氨酸)的重要特征。本研究深入了解了海洋双壳贝类中氧化应激和细胞凋亡的细胞和分子机制,并强调了代谢组学技术在海洋生物免疫毒理学研究中的适用性和可靠性。

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