ZIK plasmatis, Leibniz Institute for Plasma Science and Technology (INP), Felix-Hausdorff-Str. 2, 17489, Greifswald, Germany; Department of General Pathology, State University of Londrina, Rodovia Celso Garcia Cid, Londrina, 86047970, Brazil.
ZIK plasmatis, Leibniz Institute for Plasma Science and Technology (INP), Felix-Hausdorff-Str. 2, 17489, Greifswald, Germany; Institute of Biological Information Processing-Bioelectronics (IBI3), Forschungszentrum Juelich, Wilhelm-Johnen-Str., 52428, Jülich, Germany.
Chemosphere. 2024 May;355:141813. doi: 10.1016/j.chemosphere.2024.141813. Epub 2024 Apr 3.
The environmental presence of nano- and micro-plastic particles (NMPs) is suspected to have a negative impact on human health. Environmental NMPs are difficult to sample and use in life science research, while commercially available plastic particles are too morphologically uniform. Additionally, this NMPs exposure exhibited biological effects, including cell internalization, oxidative stress, inflammation, cellular adaptation, and genotoxicity. Therefore, developing new methods for producing heterogenous NMPs as observed in the environment is important as reference materials for research. Thus, we aimed to generate and characterize NMPs suspensions using a modified ultrasonic protocol and to investigate their biological effects after exposure to different human cell lines. To this end, we produced polyethylene terephthalate (PET) NMPs suspensions and characterized the particles by dynamic light scattering and scanning electron microscopy. Ultrasound treatment induced polymer degradation into smaller and heterogeneous PET NMPs shape fragments with similar surface chemistry before and after treatment. A polydisperse suspension of PET NMPs with 781 nm in average size and negative surface charge was generated. Then, the PET NMPs were cultured with two human cell lines, A549 (lung) and HaCaT (skin), addressing inhalation and topical exposure routes. Both cell lines interacted with and have taken up PET NMPs as quantified via cellular granularity assay. A549 but not HaCaT cell metabolism, viability, and cell death were affected by PET NMPs. In HaCaT keratinocytes, large PET NMPs provoked genotoxic effects. In both cell lines, PET NMPs exposure affected oxidative stress, cytokine release, and cell morphology, independently of concentration, which we could relate mechanistically to Nrf2 and autophagy activation. Collectively, we present a new PET NMP generation model suitable for studying the environmental and biological consequences of exposure to this polymer.
环境中纳米和微塑料颗粒(NMPs)的存在被怀疑对人类健康有负面影响。环境 NMPs 难以采样,也难以用于生命科学研究,而商业上可用的塑料颗粒在形态上过于均匀。此外,这种 NMPs 暴露表现出生物效应,包括细胞内化、氧化应激、炎症、细胞适应和遗传毒性。因此,开发新的方法来生产环境中观察到的异质 NMPs 作为研究的参考材料非常重要。因此,我们旨在使用改良的超声方案生成和表征 NMPs 悬浮液,并研究它们在暴露于不同人类细胞系后的生物学效应。为此,我们生产了聚对苯二甲酸乙二醇酯(PET)NMPs 悬浮液,并通过动态光散射和扫描电子显微镜对颗粒进行了表征。超声处理将聚合物降解为更小且异质的 PET NMPs 形状碎片,其表面化学性质在处理前后相似。生成了具有 781nm 平均粒径和负表面电荷的 PET NMPs 多分散悬浮液。然后,将 PET NMPs 与两种人类细胞系 A549(肺)和 HaCaT(皮肤)共培养,分别模拟吸入和局部暴露途径。两种细胞系都与 PET NMPs 相互作用并摄取了 PET NMPs,这通过细胞粒度测定法进行了量化。A549 但不是 HaCaT 细胞的代谢、活力和细胞死亡受到了 PET NMPs 的影响。在 HaCaT 角质形成细胞中,大的 PET NMPs 引起了遗传毒性效应。在两种细胞系中,PET NMPs 暴露均影响氧化应激、细胞因子释放和细胞形态,这与浓度无关,我们可以将其与 Nrf2 和自噬激活相关联。总的来说,我们提出了一种新的 PET NMP 生成模型,适用于研究暴露于这种聚合物的环境和生物学后果。