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利用毒理基因组学分析多氟化合物和全氟化合物对稀有鮈鲫原代培养肝细胞的联合效应

Combined effects of polyfluorinated and perfluorinated compounds on primary cultured hepatocytes from rare minnow (Gobiocypris rarus) using toxicogenomic analysis.

作者信息

Wei Yanhong, Shi Xiongjie, Zhang Hongxia, Wang Jianshe, Zhou Bingsheng, Dai Jiayin

机构信息

Key Laboratory of Animal Ecology and Conservation Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, PR China.

出版信息

Aquat Toxicol. 2009 Oct 19;95(1):27-36. doi: 10.1016/j.aquatox.2009.07.020. Epub 2009 Aug 5.

DOI:10.1016/j.aquatox.2009.07.020
PMID:19712982
Abstract

Polyfluorinated and perfluorinated compounds (PFCs) are used in numerous commercial products and have been ubiquitously detected in the environment as well as in the blood of humans and wildlife. To assess the combined effects caused by PFCs in mixtures, gene expression profiles were generated using a custom cDNA microarray to detect changes in primary cultured hepatocytes of rare minnows exposed to six individual PFCs (perfluorooctanoic acid, perfluorononanoic acid, perfluorodecanoic acid, perfluorododecanoic acid, perfluorooctane sulfonate, and 8:2 fluorotelomer alcohol) and four formulations of the PFCs mixtures. Mixtures as well as individual compounds consistently regulated a particular gene set, which suggests that these conserved genes may play a central role in the toxicity mediated by PFCs. Specifically, a number of genes regulated by the mixtures were identified in this study, which were not affected by exposure to any single component. These genes are implicated in multiple biological functions and processes, including fatty acid metabolism and transport, xenobiotic metabolism, immune responses, and oxidative stress. More than 80% of the altered genes in the PFOA- and PFOS-dominant mixture groups were of the same gene set, while the gene expression profiles from single PFOA and PFOS exposures were not as similar. This work contributes to the development of toxicogenomic approaches in combined toxicity assessment and allows for comprehensive insights into the combined action of PFCs mixtures in multiple environmental matrices.

摘要

多氟化合物和全氟化合物(PFCs)被用于众多商业产品中,并且已在环境以及人类和野生动物的血液中被广泛检测到。为了评估PFCs混合物所造成的联合效应,利用定制的cDNA微阵列生成基因表达谱,以检测暴露于六种单一PFCs(全氟辛酸、全氟壬酸、全氟癸酸、全氟十二烷酸、全氟辛烷磺酸和8:2氟调聚物醇)以及四种PFCs混合物配方的稀有鮈鲫原代培养肝细胞中的变化。混合物以及单一化合物均一致地调控特定的基因集,这表明这些保守基因可能在PFCs介导的毒性中发挥核心作用。具体而言,本研究鉴定出了一些受混合物调控但不受任何单一成分暴露影响的基因。这些基因涉及多种生物学功能和过程,包括脂肪酸代谢与转运、外源性物质代谢、免疫反应和氧化应激。在以全氟辛酸和全氟辛烷磺酸为主的混合物组中,超过80%的基因变化属于同一基因集,而单一全氟辛酸和全氟辛烷磺酸暴露的基因表达谱则没有那么相似。这项工作有助于毒理基因组学方法在联合毒性评估中的发展,并能全面洞察PFCs混合物在多种环境基质中的联合作用。

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