German Federal Institute for Risk Assessment, Max-Dohrn-Str. 8-10, 10589, Berlin, Germany.
Systems Medicine, Jacqui Wood Cancer Centre, School of Medicine, Ninewells Hospital, University of Dundee, Dundee, DD1 9SY, UK.
Arch Toxicol. 2019 Jul;93(7):1817-1833. doi: 10.1007/s00204-019-02478-7. Epub 2019 May 28.
Evidence exists that humans are exposed to plastic microparticles via diet. Data on intestinal particle uptake and health-related effects resulting from microplastic exposure are scarce. Aim of the study was to analyze the uptake and effects of microplastic particles in human in vitro systems and in rodents in vivo. The gastrointestinal uptake of microplastics was studied in vitro using the human intestinal epithelial cell line Caco-2 and thereof-derived co-cultures mimicking intestinal M-cells and goblet cells. Different sizes of spherical fluorescent polystyrene (PS) particles (1, 4 and 10 µm) were used to study particle uptake and transport. A 28-days in vivo feeding study was conducted to analyze transport at the intestinal epithelium and oxidative stress response as a potential consequence of microplastic exposure. Male reporter gene mice were treated three times per week by oral gavage with a mixture of 1 µm (4.55 × 10 particles), 4 µm (4.55 × 10 particles) and 10 µm (1.49 × 10 particles) microplastics at a volume of 10 mL/kg/bw. Effects of particles on macrophage polarization were investigated using the human cell line THP-1 to detect a possible impact on intestinal immune cells. Altogether, the results of the study demonstrate the cellular uptake of a minor fraction of particles. In vivo data show the absence of histologically detectable lesions and inflammatory responses. The particles did not interfere with the differentiation and activation of the human macrophage model. The present results suggest that oral exposure to PS microplastic particles under the chosen experimental conditions does not pose relevant acute health risks to mammals.
有证据表明,人类通过饮食摄入塑料微粒。关于肠道颗粒摄取以及微塑料暴露导致的健康影响的数据还很缺乏。本研究的目的是分析人类体外和体内实验中小塑料颗粒的摄取和影响。本研究采用人肠上皮细胞系 Caco-2 及其模拟肠道 M 细胞和杯状细胞的共培养物,在体外研究了微塑料的胃肠道摄取。使用不同大小的球形荧光聚苯乙烯(PS)颗粒(1、4 和 10 µm)研究颗粒摄取和转运。进行了 28 天的体内喂养研究,以分析肠道上皮细胞的转运和氧化应激反应,作为微塑料暴露的潜在后果。雄性报告基因小鼠每周经口灌胃 3 次,用 1 µm(4.55×10 个颗粒)、4 µm(4.55×10 个颗粒)和 10 µm(1.49×10 个颗粒)微塑料混合物处理,体积为 10 mL/kg/bw。使用人源细胞系 THP-1 研究颗粒对巨噬细胞极化的影响,以检测其对肠道免疫细胞的可能影响。总的来说,研究结果表明细胞对一小部分颗粒的摄取。体内数据显示没有组织学上可检测到的病变和炎症反应。这些颗粒没有干扰人巨噬细胞模型的分化和激活。本研究结果表明,在所选实验条件下,经口摄入 PS 微塑料颗粒不会对哺乳动物造成明显的急性健康风险。