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工程纳米材料诱导的体内表观遗传效应:以氧化铜和激光打印机排放的工程纳米颗粒为例

In vivo epigenetic effects induced by engineered nanomaterials: A case study of copper oxide and laser printer-emitted engineered nanoparticles.

作者信息

Lu Xiaoyan, Miousse Isabelle R, Pirela Sandra V, Moore Jodene K, Melnyk Stepan, Koturbash Igor, Demokritou Philip

机构信息

a Center for Nanotechnology and Nanotoxicology, Department of Environmental Health, Harvard T. H. Chan School of Public Health , Boston , MA , USA .

b Department of Environmental and Occupational Health , College of Public Health, University of Arkansas for Medical Sciences , Little Rock , AR , USA .

出版信息

Nanotoxicology. 2016;10(5):629-39. doi: 10.3109/17435390.2015.1108473. Epub 2015 Nov 11.

Abstract

Evidence continues to grow on potential environmental health hazards associated with engineered nanomaterials (ENMs). While the geno- and cytotoxic effects of ENMs have been investigated, their potential to target the epigenome remains largely unknown. The aim of this study is two-fold: 1) determining whether or not industry relevant ENMs can affect the epigenome in vivo and 2) validating a recently developed in vitro epigenetic screening platform for inhaled ENMs. Laser printer-emitted engineered nanoparticles (PEPs) released from nano-enabled toners during consumer use and copper oxide (CuO) were chosen since these particles induced significant epigenetic changes in a recent in vitro companion study. In this study, the epigenetic alterations in lung tissue, alveolar macrophages and peripheral blood from intratracheally instilled mice were evaluated. The methylation of global DNA and transposable elements (TEs), the expression of the DNA methylation machinery and TEs, in addition to general toxicological effects in the lung were assessed. CuO exhibited higher cell-damaging potential to the lung, while PEPs showed a greater ability to target the epigenome. Alterations in the methylation status of global DNA and TEs, and expression of TEs and DNA machinery in mouse lung were observed after exposure to CuO and PEPs. Additionally, epigenetic changes were detected in the peripheral blood after PEPs exposure. Altogether, CuO and PEPs can induce epigenetic alterations in a mouse experimental model, which in turn confirms that the recently developed in vitro epigenetic platform using macrophage and epithelial cell lines can be successfully utilized in the epigenetic screening of ENMs.

摘要

与工程纳米材料(ENM)相关的潜在环境健康危害的证据持续增加。虽然已经对ENM的基因毒性和细胞毒性作用进行了研究,但其靶向表观基因组的潜力在很大程度上仍不清楚。本研究的目的有两个:1)确定与工业相关的ENM是否能在体内影响表观基因组,以及2)验证最近开发的用于吸入性ENM的体外表观遗传筛选平台。选择了在消费者使用过程中从含纳米的墨粉中释放的激光打印机排放的工程纳米颗粒(PEP)和氧化铜(CuO),因为这些颗粒在最近的一项体外配套研究中诱导了显著的表观遗传变化。在本研究中,评估了经气管内滴注的小鼠肺组织、肺泡巨噬细胞和外周血中的表观遗传改变。评估了全局DNA和转座元件(TE)的甲基化、DNA甲基化机制和TE的表达,以及肺中的一般毒理学效应。CuO对肺表现出更高的细胞损伤潜力,而PEP表现出更强的靶向表观基因组的能力。在暴露于CuO和PEP后,观察到小鼠肺中全局DNA和TE的甲基化状态以及TE和DNA机制的表达发生改变。此外,在暴露于PEP后在外周血中检测到表观遗传变化。总之,CuO和PEP可以在小鼠实验模型中诱导表观遗传改变,这反过来证实了最近开发的使用巨噬细胞和上皮细胞系的体外表观遗传平台可以成功用于ENM的表观遗传筛选。

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本文引用的文献

1
The Fine LINE: Methylation Drawing the Cancer Landscape.
Biomed Res Int. 2015;2015:131547. doi: 10.1155/2015/131547. Epub 2015 Sep 13.
2
In Vitro Toxicity and Epigenotoxicity of Different Types of Ambient Particulate Matter.
Toxicol Sci. 2015 Dec;148(2):473-87. doi: 10.1093/toxsci/kfv200. Epub 2015 Sep 4.
3
Response of transposable elements to environmental stressors.
Mutat Res Rev Mutat Res. 2015 Jul-Sep;765:19-39. doi: 10.1016/j.mrrev.2015.05.003. Epub 2015 May 30.
4
Assessment of the lung toxicity of copper oxide nanoparticles: current status.
Nanomedicine (Lond). 2015;10(15):2365-77. doi: 10.2217/nnm.15.72. Epub 2015 Aug 7.
5
Understanding and exploiting nanoparticles' intimacy with the blood vessel and blood.
Chem Soc Rev. 2015 Nov 21;44(22):8174-99. doi: 10.1039/c5cs00499c. Epub 2015 Aug 4.
7
Short-term exposure to engineered nanomaterials affects cellular epigenome.
Nanotoxicology. 2016;10(2):140-50. doi: 10.3109/17435390.2015.1025115. Epub 2015 May 4.
8
Mechanistic Investigation of the Biological Effects of SiO₂, TiO₂, and ZnO Nanoparticles on Intestinal Cells.
Small. 2015 Jul;11(28):3458-68. doi: 10.1002/smll.201403232. Epub 2015 Apr 22.
10
Inactivation of foodborne microorganisms using engineered water nanostructures (EWNS).
Environ Sci Technol. 2015 Mar 17;49(6):3737-45. doi: 10.1021/es505868a. Epub 2015 Mar 3.

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