Hits:
Indexed by:期刊论文
Date of Publication:2012-11-06
Journal:ENVIRONMENTAL SCIENCE & TECHNOLOGY
Included Journals:SCIE、EI、PubMed、PKU、ISTIC、Scopus
Volume:46
Issue:21
Page Number:12170-12177
ISSN No.:0013-936X
Abstract:Proteomic analysis allows detection of changes of proteins expression in organisms exposed to environmental pollutants, leading to the discovery of biomarkers of exposure and understanding of the action mechanism of toxicity. In the present study, we applied iTRAQ labeling quantitative proteomic technology for global characterization of the liver proteome in mice exposed to perfluorooctane sulfonate (PFOS). This successfully identified and quantified 1038 unique proteins. Seventy-one proteins showed a significant expression change in the treated groups (1.0, 2.5, 5.0 mg/kg of body weight) compared with the control group, and 16 proteins displayed strong dose dependent changes. Gene ontology analysis showed that these differential proteins were significantly enriched and stimulus. We detected significantly increased expression levels of enzymes regulating mainly involved in lipid metabolism, transport, biosynthetic processes, and response to peroxisomal beta-oxidation-including long chain acyl-CoA synthetase, acyl-CoA oxidase 1, bifunctional enzyme, and 3-ketoacyl-CoA thiolase A. PFOS also significantly induced cytochrome P450s and glutathione S-transferases that are responsible for the metabolism of xenobiotic compounds. The expressions of several proteins with important biological functions-such as cysteine sulfinic acid decarboxylase, aldehyde dehydrogenase, and apolipoprotein A-I, also correlated with PFOS exposure. Together, the present results provide insight into the molecular mechanism and biomarkers for PFOS-induced effects.
Pre One:Response to the comments on the paper "Bioaugmentation and functional partitioning in a zero valent iron-anaerobic reactor for sulfate-containing wastewater treatment"
Next One:Colloidal Graphene as a Transducer in Homogeneous Fluorescence-Based Immunosensor for Rapid and Sensitive Analysis of Microcystin-LR