Wei Yanhong, Chan Leo L, Wang Dazhi, Zhang Hongxia, Wang Jianshe, Dai Jiayin
Key Laboratory of Animal Ecology and Conservation Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, P.R. China.
J Proteome Res. 2008 Apr;7(4):1729-39. doi: 10.1021/pr7008059. Epub 2008 Feb 28.
Perfluorooctanoic acid (PFOA) is a ubiquitous contaminant that has been shown to lead to hepatoxicity and is implicated in the incidence of liver tumors in mammals. A number of previous studies have described the toxic effects of PFOA based on conventional toxicological indices and transcriptional data. However, little evidence on protein levels is available. To further our understanding of mechanisms of action and identify the potential protein biomarkers for PFOA exposure, two-dimensional electrophoresis coupled with mass spectrometry has been used to identify proteins differentially expressed in the livers of rare minnow ( Gobiocypris rarus) following PFOA exposure of 3, 10, and 30 mg/L. After comparison of the protein profiles from treated and control groups, 34 and 48 protein spots were found altered in abundance (> 2-fold) from males and females, respectively. Matrix-assisted laser desorption/ionization (MALDI) tandem time-of-flight mass spectrometry (TOF/TOF) analysis allowed the unambiguous identification of 25 spots, corresponding to 22 different proteins. These proteins were involved in intracellular fatty acid transport, oxidative stress, macromolecule catabolism, the cell cycle, maintenance of intracellular Ca2+ homeostasis, and mitochondrial function. In addition, marked gender differences in response to PFOA have been well-described from the comparison of the male and female protein profiles. Transcriptional analysis of nine mRNAs encoding proteins altered by PFOA in the proteome analysis was determined by real-time PCR. The consistent and discrepant results between mRNA and protein levels suggested that complicated regulatory mechanisms of gene expression were implicated in the response to PFOA exposure.
全氟辛酸(PFOA)是一种普遍存在的污染物,已被证明会导致肝毒性,并与哺乳动物肝脏肿瘤的发生有关。此前的一些研究已根据传统毒理学指标和转录数据描述了PFOA的毒性作用。然而,关于蛋白质水平的证据很少。为了进一步了解其作用机制并确定PFOA暴露的潜在蛋白质生物标志物,二维电泳结合质谱已被用于鉴定稀有鮈鲫(Gobiocypris rarus)在3、10和30mg/L PFOA暴露后肝脏中差异表达的蛋白质。比较处理组和对照组的蛋白质谱后,发现雄性和雌性分别有34个和48个蛋白质斑点丰度改变(>2倍)。基质辅助激光解吸/电离(MALDI)串联飞行时间质谱(TOF/TOF)分析明确鉴定出25个斑点,对应22种不同蛋白质。这些蛋白质参与细胞内脂肪酸转运、氧化应激、大分子分解代谢、细胞周期、细胞内Ca2+稳态维持以及线粒体功能。此外,通过比较雄性和雌性蛋白质谱,已充分描述了对PFOA反应中明显的性别差异。通过实时PCR对蛋白质组分析中9种因PFOA而改变的蛋白质的mRNA进行转录分析。mRNA和蛋白质水平之间一致和不一致的结果表明,基因表达的复杂调控机制与对PFOA暴露的反应有关。