Key Laboratory of Animal Ecology and Conservation Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, PR China.
Environ Int. 2012 Jul;42:20-30. doi: 10.1016/j.envint.2011.03.002. Epub 2011 Apr 9.
Perfluorononanoic acid (PFNA), a synthetic perfluorinated carboxylic acid and fluorosurfactant, is a known environmental contaminant found in people and wildlife. To understand the hepatotoxicity mechanism of PFNA, male zebrafish (n=200) were exposed to differing concentrations of PFNA (0, 0.1, 0.5, and 1.0 mg/L) for 180 days. A two-dimensional difference gel electrophoresis (2-D DIGE) approach coupled with MALDI-TOF-MS/MS analysis was employed to detect and identify the differential expressed proteins. A total of 57 proteins were successfully identified and categorized into functional classes that included metabolism (amino acid metabolism, TCA cycle and pyruvate metabolism, gluconeogenesis and glycolysis, protein metabolism and modification, and nucleotides metabolism), structure and motility, stress and defense, signal transduction, and cell communication. Our proteomic analyses added new perspective to PFNA hepatotoxicity in zebrafish. Results regarding mRNA levels demonstrated that the involvement of peroxisome proliferator-activated receptors (PPARs) could not sufficiently explain the hepatotoxicity mechanism of PFAAs in zebrafish. The extensive protein variations indicated that multiple cellular pathways were involved in and suggested that multiple protein molecules should be simultaneously targeted as an effective strategy to counter PFNA toxicity. Other potential modes should be further investigated.
全氟壬酸(PFNA),一种合成的全氟羧酸和氟表面活性剂,是一种已知的环境污染物,存在于人类和野生动物中。为了了解 PFNA 的肝毒性机制,将雄性斑马鱼(n=200)暴露于不同浓度的 PFNA(0、0.1、0.5 和 1.0 mg/L)中 180 天。采用二维差异凝胶电泳(2-D DIGE)方法结合 MALDI-TOF-MS/MS 分析来检测和鉴定差异表达的蛋白质。共成功鉴定了 57 种蛋白质,并将其归类为具有不同功能的类别,包括代谢(氨基酸代谢、TCA 循环和丙酮酸代谢、糖异生和糖酵解、蛋白质代谢和修饰以及核苷酸代谢)、结构和运动、应激和防御、信号转导和细胞通讯。我们的蛋白质组学分析为 PFNA 在斑马鱼中的肝毒性提供了新的视角。mRNA 水平的结果表明,过氧化物酶体增殖物激活受体(PPARs)的参与不能充分解释 PFAAs 在斑马鱼中的肝毒性机制。广泛的蛋白质变化表明,多个细胞途径参与其中,并表明应该同时针对多个蛋白质分子作为对抗 PFNA 毒性的有效策略。其他潜在模式应进一步研究。