Toxic responses of Perna viridis hepatopancreas exposed to DDT, benzo(a) pyrene and their mixture uncovered by iTRAQ-based proteomics and NMR-based metabolomics
Song, Qinqin1,2,3; Zhou, Hailong1,2; Han, Qian1,2; Diao, Xiaoping1,2
发表期刊AQUATIC TOXICOLOGY
ISSN0166-445X
2017-11-01
卷号192页码:48-57
关键词Benzo(a)Pyrene Ddt P. Viridis Hepatopancreas Itraq Metabolomics
研究领域Marine & Freshwater Biology ; Toxicology
DOI10.1016/j.aquatox.2017.09.010
产权排序[Song, Qinqin; Zhou, Hailong; Han, Qian; Diao, Xiaoping] Hainan Univ, State Key Lab Marine Resource Utilizat South Chin, Haikou 570228, Hainan, Peoples R China; [Song, Qinqin; Zhou, Hailong; Han, Qian; Diao, Xiaoping] Hainan Univ, Inst Trop Agr & Forestry, 58 Renmin Rd, Haikou 570228, Hainan, Peoples R China; [Song, Qinqin] Chinese Acad Sci, Yantai Inst Coastal Zone Res, Key Lab Coastal Zone Environm Proc, Yantai 264003, Peoples R China
作者部门中国科学院海岸带环境过程重点实验室
英文摘要Dichlorodiphenyltrichloroethane (DDT) and benzo(a)pyrene (BaP) are environmental estrogens (EEs) that are ubiquitous in the marine environment. In the present study, we integrated isobaric tags for relative and absolute quantitation (iTRAQ)-based proteomic and nuclear magnetic resonance (NMR)-based metabolomic approaches to explore the toxic responses of green mussel hepatopancreas exposed to DDT (10 mu g/L), BaP (10 mu g/L) and their mixture. The metabolic responses indicated that BaP primarily disturbed energy metabolism and osmotic regulation in the hepatopancreas of the male green mussel P. viridis. Both DDT and the mixture of DDT and BaP perturbed the energy metabolism and osmotic regulation in P. viridis. The proteomic responses revealed that BaP affected the proteins involved in energy metabolism, material transformation, cytoskeleton, stress responses, reproduction and development in green mussels. DDT exposure could change the proteins involved in primary metabolism, stress responses, cytoskeleton and signal transduction. However, the mixture of DDT and BaP altered proteins associated with material and energy metabolism, stress responses, signal transduction, reproduction and development, cytoskeleton and apoptosis. This study showed that iTRAQ-based proteomic and NMR-based metabolomic approaches could effectively elucidate the essential molecular mechanism of disturbances in hepatopancreas function of green mussels exposed to environmental estrogens.
文章类型Article
资助机构National Natural Science Foundation of China(41161077, 31760164) ; Specialized Research Fund for the Midwest Program of Hainan University(ZXBJH-XK002)
收录类别SCI
语种英语
关键词[WOS]MUSSEL MYTILUS-GALLOPROVINCIALIS ; CLAM RUDITAPES-PHILIPPINARUM ; EARTHWORM EISENIA-FOETIDA ; OYSTER CRASSOSTREA-GIGAS ; HEAT-SHOCK PROTEINS ; GENDER-SPECIFIC RESPONSES ; 2,2',4,4'-TETRABROMODIPHENYL ETHER ; PETROCHEMICAL CONTAMINATION ; H-1-NMR SPECTROSCOPY ; SALINITY ACCLIMATION
研究领域[WOS]Marine & Freshwater Biology ; Toxicology
WOS记录号WOS:000415768700007
引用统计
被引频次:15[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.yic.ac.cn/handle/133337/24046
专题中国科学院烟台海岸带研究所知识产出
通讯作者Zhou, Hailong
作者单位1.Hainan Univ, State Key Lab Marine Resource Utilizat South Chin, Haikou 570228, Hainan, Peoples R China
2.Hainan Univ, Inst Trop Agr & Forestry, 58 Renmin Rd, Haikou 570228, Hainan, Peoples R China
3.Chinese Acad Sci, Yantai Inst Coastal Zone Res, Key Lab Coastal Zone Environm Proc, Yantai 264003, Peoples R China
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GB/T 7714
Song, Qinqin,Zhou, Hailong,Han, Qian,et al. Toxic responses of Perna viridis hepatopancreas exposed to DDT, benzo(a) pyrene and their mixture uncovered by iTRAQ-based proteomics and NMR-based metabolomics[J]. AQUATIC TOXICOLOGY,2017,192:48-57.
APA Song, Qinqin,Zhou, Hailong,Han, Qian,&Diao, Xiaoping.(2017).Toxic responses of Perna viridis hepatopancreas exposed to DDT, benzo(a) pyrene and their mixture uncovered by iTRAQ-based proteomics and NMR-based metabolomics.AQUATIC TOXICOLOGY,192,48-57.
MLA Song, Qinqin,et al."Toxic responses of Perna viridis hepatopancreas exposed to DDT, benzo(a) pyrene and their mixture uncovered by iTRAQ-based proteomics and NMR-based metabolomics".AQUATIC TOXICOLOGY 192(2017):48-57.
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