Tavakolpournegari Alireza, Annangi Balasubramanyam, Villacorta Aliro, Banaei Gooya, Martin Joan, Pastor Susana, Marcos Ricard, Hernández Alba
Group of Mutagenesis, Department of Genetics and Microbiology, Faculty of Biosciences, Universitat Autònoma de Barcelona, Cerdanyola Del Vallès, Barcelona, Spain.
Group of Mutagenesis, Department of Genetics and Microbiology, Faculty of Biosciences, Universitat Autònoma de Barcelona, Cerdanyola Del Vallès, Barcelona, Spain; Facultad de Recursos Naturales Renovables, Universidad Arturo Prat, Iquique, Chile.
Chemosphere. 2023 Jun;325:138360. doi: 10.1016/j.chemosphere.2023.138360. Epub 2023 Mar 10.
The environmental presence of micro/nanoplastics (MNPLs) is an environmental and human health concern. Such MNPLs can result from the physicochemical/biological degradation of plastic goods (secondary MNPLs) or can result from industrial production at that size, for different commercial purposes (primary MNPLs). Independently of their origin, the toxicological profile of MNPLs can be modulated by their size, as well as by the ability of cells/organisms to internalize them. To get more information on these topics we have determined the ability of three different sizes of polystyrene MNPLs (50, 200, and 500 nm) to produce different biological effects in three different human hematopoietic cell lines (Raji-B, THP-1, and TK6). Results show that none of the three sizes was able to induce toxicity (growth ability) in any of the tested cell types. Although transmission electron microscopy and confocal images showed cell internalization in all the cases, their quantification by flow cytometry demonstrated an important uptake by Raji-B and THP-1 cells, in comparison with TK6 cells. For the first ones, the uptake was negatively associated with the size. Interestingly, when the loss of mitochondrial membrane potential was determined, dose-related effects were observed for Raji-B and THP-1 cells, but not for TK6 cells. These effects were observed for the three different sizes. Finally, when oxidative stress induction was evaluated, no clear effects were observed for the different tested combinations. Our conclusion is that size, biological endpoint, and cell type are aspects modulating the toxicological profile of MNPLs.
微/纳米塑料(MNPLs)在环境中的存在是一个环境和人类健康问题。此类MNPLs可能源于塑料制品的物理化学/生物降解(次生MNPLs),也可能源于出于不同商业目的的该尺寸工业生产(原生MNPLs)。无论其来源如何,MNPLs的毒理学特征可受其尺寸以及细胞/生物体摄取它们的能力的调节。为了获取有关这些主题的更多信息,我们测定了三种不同尺寸的聚苯乙烯MNPLs(50、200和500纳米)在三种不同人类造血细胞系(Raji-B、THP-1和TK6)中产生不同生物学效应的能力。结果表明,这三种尺寸的MNPLs均无法在任何测试细胞类型中诱导毒性(生长能力)。尽管透射电子显微镜和共聚焦图像显示在所有情况下细胞都有摄取,但与TK6细胞相比,通过流式细胞术对其进行定量分析表明,Raji-B和THP-1细胞有大量摄取。对于前两种细胞,摄取与尺寸呈负相关。有趣的是,当测定线粒体膜电位的丧失时,观察到Raji-B和THP-1细胞有剂量相关效应,但TK6细胞没有。在三种不同尺寸的MNPLs中均观察到了这些效应。最后,当评估氧化应激诱导时,对于不同的测试组合未观察到明显效应。我们的结论是,尺寸、生物学终点和细胞类型是调节MNPLs毒理学特征的因素。