Unité de Recherche en Biologie des Organismes (URBO), The University of Namur (FUNDP), Rue de Bruxelles 61, B-5000 Namur, Belgium.
Aquat Toxicol. 2011 May;103(1-2):1-8. doi: 10.1016/j.aquatox.2011.01.015. Epub 2011 Feb 2.
The environmental persistence, bioaccumulative tendency and potential toxicity of perfluorooctane sulfonate (PFOS) have generated great concern. This study aimed at evaluating the toxicity of short-term PFOS exposure in gills of the European bullhead Cottus gobio, a candidate sentinel species, by monitoring the response of some enzymes (citrate synthase CS, cytochrome c oxidase CCO, and lactate dehydrogenase LDH), and by undertaking a proteomic analysis using 2D-DIGE. First, a 96-h exposure to 1mg PFOS/L significantly altered the activity of mitochondrial CS and CCO. Second, 2D-DIGE gels were used to compare gills from the control fish group with tissues from fish exposed for 96h to either 0.1 or 1mg PFOS/L. From the 27 protein spots displaying significant changes in abundance following PFOS exposure, a total of 20 different proteins were identified using nano LC-MS/MS and the Peptide and Protein Prophet of Scaffold software. The differentially expressed proteins that were identified are involved in the general stress response, ubiquitin-proteasome system, energy metabolism, and actin cytoskeleton, which provide clues on the cellular pathways and components mainly affected by PFOS. Moreover, our results showed that most proteins were differentially expressed at the low but not at the high PFOS concentration. This work provides insights into the biochemical and molecular events in PFOS-induced toxicity in gill tissue, and suggests that further studies on the identified proteins could provide crucial information to better understand the mechanisms of PFOS toxicity in fish.
全氟辛烷磺酸 (PFOS) 的环境持久性、生物蓄积倾向和潜在毒性引起了极大的关注。本研究旨在通过监测一些酶(柠檬酸合酶 CS、细胞色素 c 氧化酶 CCO 和乳酸脱氢酶 LDH)的反应,以及使用 2D-DIGE 进行蛋白质组分析,来评估欧洲七鳃鳗鳃组织中 PFOS 短期暴露的毒性。首先,96 小时暴露于 1mg PFOS/L 显著改变了线粒体 CS 和 CCO 的活性。其次,使用 2D-DIGE 凝胶比较了暴露于 0.1 或 1mg PFOS/L 96 小时的对照组鱼和组织的鳃。从暴露于 PFOS 后丰度发生显著变化的 27 个蛋白质斑点中,使用 nano LC-MS/MS 和 Scaffold 软件的 Peptide and Protein Prophet 共鉴定出 20 种不同的蛋白质。鉴定出的差异表达蛋白参与一般应激反应、泛素-蛋白酶体系统、能量代谢和肌动蛋白细胞骨架,为 PFOS 主要影响的细胞途径和成分提供了线索。此外,我们的结果表明,大多数蛋白质在低浓度而不是高浓度 PFOS 下差异表达。这项工作深入了解了 PFOS 诱导毒性在鳃组织中的生化和分子事件,并表明对鉴定出的蛋白质进行进一步研究可以提供关键信息,以更好地理解鱼类中 PFOS 毒性的机制。