Verdile Nicole, Cattaneo Nico, Camin Federica, Zarantoniello Matteo, Conti Federico, Cardinaletti Gloriana, Brevini Tiziana A L, Olivotto Ike, Gandolfi Fulvio
Department of Veterinary Medicine and Animal Sciences, University of Milan, 26900 Lodi, Italy.
Department of Life and Environmental Sciences, Marche Polytechnic University, 60131 Ancona, Italy.
Cells. 2025 Jan 3;14(1):44. doi: 10.3390/cells14010044.
Microplastics (MPs) in fish can cross the intestinal barrier and are often bioaccumulated in several tissues, causing adverse effects. While the impacts of MPs on fish are well documented, the mechanisms of their cellular internalization remain unclear. A rainbow-trout () intestinal platform, comprising proximal and distal intestinal epithelial cells cultured on an Alvetex scaffold, was exposed to 50 mg/L of MPs (size 1-5 µm) for 2, 4, and 6 h. MP uptake was faster in RTpi-MI compared to RTdi-MI. Exposure to microplastics compromised the cellular barrier integrity by disrupting the tight-junction protein zonula occludens-1, inducing significant decreases in the transepithelial-electrical-resistance (TEER) values. Consequently, MPs were internalized by cultured epithelial cells and fibroblasts. The expression of genes related to endocytosis (, ), macropinocytosis (), and tight junctions' formation (, , ) was analyzed. No significant differences were observed in , , and expression, while an upregulation of , , and genes was detected, suggesting macropinocytosis as the route of internalization, since also and are indirectly related to this mechanism. The obtained results are consistent with data previously reported in vivo, confirming its validity for identifying MP internalization pathways. This could help to develop strategies to mitigate MP absorption through ingestion.
鱼类体内的微塑料(MPs)能够穿过肠道屏障,并常常在多个组织中生物蓄积,从而产生不利影响。虽然MPs对鱼类的影响已有充分记录,但其细胞内化机制仍不清楚。将一个由培养在Alvetex支架上的近端和远端肠上皮细胞组成的虹鳟鱼肠道平台暴露于50 mg/L的MPs(尺寸为1 - 5 µm)中2、4和6小时。与RTdi - MI相比,RTpi - MI对MP的摄取更快。暴露于微塑料会破坏紧密连接蛋白闭合蛋白-1,从而损害细胞屏障完整性,导致跨上皮电阻(TEER)值显著降低。因此,MPs被培养的上皮细胞和成纤维细胞内化。分析了与内吞作用( 、 )、巨胞饮作用( )和紧密连接形成( 、 、 )相关的基因表达。在 、 和 的表达上未观察到显著差异,而检测到 、 和 基因上调,这表明巨胞饮作用是内化途径,因为 和 也与该机制间接相关。所得结果与先前体内报道的数据一致,证实了其在识别MP内化途径方面的有效性。这有助于制定减轻通过摄食吸收MP的策略。