Con fi rmatory assays for transient changes of omics in soil invertebrates - Copper materials in a multigenerational exposure

被引:20
作者
Bicho, Rita C. [1 ,2 ]
Faustino, A. M. R. [3 ]
Rema, A. [3 ]
Scott-Fordsmand, Janeck J. [4 ]
Amorim, Monica J. B. [1 ,2 ]
机构
[1] Univ Aveiro, Dept Biol, P-3810193 Aveiro, Portugal
[2] Univ Aveiro, CESAM, P-3810193 Aveiro, Portugal
[3] Univ Porto, Biomed Sci Inst Abel Salazar, Dept Pathol & Mol Immunol, P-4050313 Porto, Portugal
[4] Aarhus Univ, Dept Biosci, Vejlsovej 25,POB 314, DK-8600 Silkeborg, Denmark
关键词
Nanospecific effect; Adverse outcome pathway (AOP); Nanoecotoxicology; Oligochaeta; Long term; Epigenetics; FULL LIFE-CYCLE; ENCHYTRAEIDAE OLIGOCHAETA; ZEBRAFISH EMBRYOS; FOLSOMIA-CANDIDA; NANOPARTICLES; TOXICITY; EXPRESSION; RESPONSES; CADMIUM; METALLOTHIONEIN;
D O I
10.1016/j.jhazmat.2020.123500
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Environmental risk assessment (ERA) based on effects caused by chronic and longer term exposure is highly relevant. Further, if mechanistic based approaches (e.g. omics) can be included, beyond apical endpoints (e.g. reproduction), the prediction of effects increases. For Cu NMs (and CuCl2) this has been studied in detail, covering multi-omics and apical effects using the soil standard species Enchytraeus crypticus. The intermediate level effects like cell/tissue and organ alterations represent a missing link. In the present study we aimed to: 1) perform long term exposure to Cu materials (full life cycle and multigeneration, 46 and 224 days) to collect samples; 2) perform histology and immunohistochemistry on collected samples at 12 time points and 17 treatments; 3) integrate all levels of biological organization onto an adverse outcome pathway (AOP) framework. CuO NMs and CuCl2 caused both similar and different stress response, either at molecular initiating events (MIE) or key events (KEs) of higher level of biological organization. Cell/Tissue and organ level, post-transcriptional and transcriptional mechanisms, through histone modifications and microRNA related protein, were similarly affected. While both Cu forms affected the Notch signalling pathway, CuCl2 also caused oxidative stress. Different mechanisms of DNA methylation (epigenetics) were activated by CuO NMs and CuCl2 at the MIE.
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页数:9
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