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Alteration of Heart Tissue Protein Profiles in Acute Cadmium-Treated Scallops Patinopecten yessoensis

机译:急性镉处理过的扇贝Patinopecten yessoensis心脏组织蛋白质谱的变化

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Cadmium (Cd) is an extremely toxic metal that induces a wide spectrum of toxic responses in organisms in the environment. In the present study, scallops (Patinopecten yessoensis), after acclimation for 1 week in the laboratory, were subjected to acute Cd chloride (CdCl2) toxicity, and ultramorphological and proteomic changes in their heart tissues were analyzed and compared with those of the nonexposed control group. Electron microscopy showed that ultrastructures of the cytoplasm and mitochondria in scallop hearts were badly damaged, and two-dimensional gel electrophoresis showed 32 protein spots that were differentially expressed after exposure to 10 mg/l CdCl2 for 24 h. Of these spots, 8 were upregulated, 16 were downregulated, and 8 showed low expression. Proteins from these spots were identified using matrix-assisted laser desorption/ionization-time of flight mass spectrometry and database searching. The results indicated that these proteins are involved in the regulation of cell structure, transport, signal transduction, and metabolism. Among other things, four proteins―identified as amino acid adenosine triphosphate (ATP)–binding cassette transporter, glycerol-3-phosphate dehydrogenase (nicotinamide adenine dinucleotide phosphate), nicotinamide adenine dinucleotide oxidase, and ATPase―were demonstrated to be especially associated with Cd toxicity. Some of the other proteins observed in this work are of particular interest in terms of their responses to Cd, which have not been reported previously. These data may provide novel biomarkers for monitoring the Cd contamination level of flowing seawater as well as provide useful insights into the mechanisms of Cd toxicity.
机译:镉(Cd)是一种剧毒金属,在环境中的生物中引起广泛的毒性反应。在本研究中,扇贝(Patinopecten yessoensis)在实验室适应1周后,受到了急性Cd氯化物(CdCl 2 )的毒性作用,并分析了其心脏组织的超形态学和蛋白质组学变化并与未暴露对照组进行比较。电镜观察发现扇贝心脏细胞质和线粒体的超微结构受到严重破坏,二维凝胶电泳显示32个蛋白质斑点在暴露于10 mg / l CdCl 2 24 h后差异表达。 。在这些斑点中,有8个被上调,有16个被下调,并且8个显示低表达。使用基质辅助激光解吸/电离飞行时间质谱和数据库搜索来鉴定来自这些斑点的蛋白质。结果表明这些蛋白质参与细胞结构,转运,信号转导和代谢的调节。除其他外,证实了四种蛋白质-被鉴定为氨基酸三磷酸腺苷(ATP)结合盒式转运蛋白,3-磷酸甘油脱氢酶(烟酰胺腺嘌呤二核苷酸磷酸),烟酰胺腺嘌呤二核苷酸氧化酶和ATPase与Cd尤其相关。毒性。在这项工作中观察到的其他一些蛋白质,由于它们对Cd的反应特别受关注,以前没有报道过。这些数据可以提供新颖的生物标记物,用于监测流动的海水中Cd污染水平,并提供有关Cd毒性机理的有用见解。

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