Impact of perfluorooctanesulfonate and perfluorooctanoic acid on human peripheral leukocytes

被引:70
作者
Brieger, Anne [1 ]
Bienefeld, Nicole [1 ]
Hasan, Rafah [1 ]
Goerlich, Roland [1 ]
Haase, Hajo [1 ]
机构
[1] Rhein Westfal TH Aachen, Inst Immunol, Fac Med, D-52074 Aachen, Germany
关键词
Perfluorinated compound; Perfluorooctanesulfonate; Perfluorooctanoic acid; Immunotoxicity; Leukocytes; Lymphocytes; ACTIVATED RECEPTOR-ALPHA; SULFONATE PFOS EXPOSURE; SHORT-TERM EXPOSURE; FEMALE B6C3F1 MICE; AMMONIUM PERFLUOROOCTANOATE; PEROXISOME PROLIFERATOR; PPAR-ALPHA; CYNOMOLGUS MONKEYS; HUMORAL IMMUNITY; DIETARY TOXICITY;
D O I
10.1016/j.tiv.2011.03.005
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Perfluorinated compounds (PFCs), such as perfluorooctanesulfonate (PFOS) and perfluorooctanoic acid (PFOA), are xenobiotics that can be detected worldwide in the environment, wildlife, and humans. So far, the immunotoxicity of PFCs has only been investigated in rodents, but not in humans. In this study, we explore the impact of PFOS and PFOA on selected functions of human leukocytes in vitro. PFOS induced a significant decrease of natural killer-cell activity and reduced the release of the pro-inflammatory cytokine TNF-alpha following lipopolysaccharide (LPS)-stimulation. Furthermore, the plasma PFOS concentrations (2.09-8.98 ng/ml) found in our study subjects correlated positively with the LPS-stimulated IL-6 release. PFOA augmented significantly calcitriol-induced monocytic differentiation of the HL-60 cell line. Additionally, there was a significant linear relationship between LPS-stimulated TNF-alpha and IL-6 release, and the plasma PFOA (1.20-6.92 ng/ml) concentrations of the study subjects. In conclusion, the investigated PFCs affect human immune cells mainly with regard to natural killer-cell cytotoxicity and the pro-inflammatory cytokine release by stimulated macrophages. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:960 / 968
页数:9
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