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首页> 外文期刊>Fish & Shellfish Immunology >Copper-induced oxidative damage to the prophenoloxidase-activating system in the freshwater crayfish Procambarus clarkii
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Copper-induced oxidative damage to the prophenoloxidase-activating system in the freshwater crayfish Procambarus clarkii

机译:铜诱导的淡水小龙虾克氏原螯虾中前酚氧化酶激活系统的氧化损伤

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Previous studies have demonstrated copper-induced proteins damage in gill and hepatopancreas of the freshwater crayfish Procambarus clarkii, but little information is available about its effects on key component of the innate defense in haemolymph. In the present study, we evaluated the relationship between oxidative carbonylation and prophenoloxidase-activating system (proPO-AS) activity, by exposing P. clarkii to sub-lethal concentrations (1/50, 1/12, 1/6 and 1/3 of the 96 h LC50) Cu2+ up to 96 h. Six biomarkers of oxidative stress, i.e. reactive oxygen species (ROS), superoxide dismutase (SOD), catalase (CAT), protein carbonyl (PC), malondialdehyde (MDA) and DNA-protein crosslinks (DPCs), and six indicators of immune status, i.e. total hemocyte counts (THCs), differential hemocyte counts (DHCs), hemocyanin (HC), prophenoloxidase (proPO), serine protease (SP) and phenoloxidase (PO), were determined in haemolymph. The results indicated that there was a significant increase (P 0.05) in the levels of ROS, PC, MDA and DPCs accompanied by markedly decreased (P 0.05) activities of proPO, SP, PO and HC in a dose and time dependent manner. The significant and positive correlations (P 0.01) between ROS production and the formation of PC, MDA and DPCs were observed in crayfish at 96 h. There was a significant negative correlation (P 0.01) between the levels of protein carbonyls and the activities of proPO and SP in hemocyte lysate supernatant and PO and HC in haemolymph. Carbonylated proteins may be recognized not merely as a specific signal in oxidative stress pathways but also as a "non-self" molecule in proPO-AS. In crayfish species, copper-catalyzed protein carbonylation may be one of the main mechanisms for immunity dysfunction in proPO-AS. (C) 2016 Elsevier Ltd. All rights reserved.
机译:先前的研究表明,铜诱导的蛋白质会破坏淡水小龙虾克氏原螯虾的腮和肝胰腺,但有关其对血淋巴先天防御的关键成分的影响的信息很少。在本研究中,我们通过将克氏疟原虫暴露于亚致死浓度(1 / 50、1 / 12、1 / 6和1/3)来评估氧化羰基化与酚氧化酶激活系统(proPO-AS)活性之间的关系。 96小时的LC50)Cu2 +最多96小时。氧化应激的六个生物标记,即活性氧(ROS),超氧化物歧化酶(SOD),过氧化氢酶(CAT),羰基蛋白质(PC),丙二醛(MDA)和DNA-蛋白质交联(DPC),以及六个免疫状态指标在血淋巴中测定总血细胞计数(THCs),差异血细胞计数(DHCs),血蓝蛋白(HC),酚氧化酶原(proPO),丝氨酸蛋白酶(SP)和酚氧化酶(PO)。结果表明,ROS,PC,MDA和DPC的水平显着增加(P <0.05),同时proPO,SP,PO和HC的活性显着降低(P <0.05),呈剂量和时间依赖性。 。在小龙虾96小时时,观察到ROS的产生与PC,MDA和DPC的形成之间的显着正相关(P <0.01)。血细胞裂解液上清液中的蛋白羰基水平与proPO和SP活性以及血淋巴中的PO和HC呈显着负相关(P <0.01)。羰基化的蛋白质不仅可以被识别为氧化应激途径中的特定信号,而且还可以被视为proPO-AS中的“非自身”分子。在小龙虾物种中,铜催化的蛋白质羰基化可能是proPO-AS免疫功能障碍的主要机制之一。 (C)2016 Elsevier Ltd.保留所有权利。

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