Nanoplastics activate a TLR4/p38-mediated pro-inflammatory response in human intestinal and mouse microglia cells

被引:22
作者
Antunes, Joana [1 ,2 ]
Sobral, Paula [1 ,2 ]
Martins, Marta [1 ,2 ]
Branco, Vasco [3 ,4 ]
机构
[1] Univ Nova Lisboa, Marine & Environm Sci Ctr, NOVA Sch Sci & Technol FCT NOVA, MARE, P-2829516 Caparica, Portugal
[2] Univ Nova Lisboa, NOVA Sch Sci & Technol FCT NOVA, Dept Sci & Environm Engn, Aquat Res Network Associated Lab,ARNET, P-2829516 Caparica, Portugal
[3] Univ Lisbon, Res Inst Med iMed ULisboa, Fac Pharm, Ave Prof Gama Pinto, P-1649003 Lisbon, Portugal
[4] Egas Moniz Sch Hlth & Sci, Egas Moniz Ctr Interdisciplinary Res CiiEM, P-2829511 Caparica, Portugal
关键词
Nanoplastics; Intestine; Inflammation; TLR4; Microglia; p38; NF-KAPPA-B; NITRIC-OXIDE; P38; MAPK; EXPRESSION; PHOSPHORYLATION; STRESS;
D O I
10.1016/j.etap.2023.104298
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The crescent presence of nanoplastics in the environment raises concerns regarding their potential impact on health. This study exposed human colon adenocarcinoma cells (HT29) and microglia cells (N9) to nanoplastics (25 nm, 50 nm, and 100 nm Polystyrene) to investigate their inflammatory responses, which are vital for body's defence. Although cytotoxicity remained generally low, HT29 cells exhibited a notable upregulation of p50 and p38 expression, concomitant with elevated TLR4 expression, in contrast with N9 cells that showed a less pro-nounced upregulation of these proteins. Additionally, nanoplastic exposure increased IL-1ss levels, partially attenuated by pre-exposure to TLR4 or p38 inhibitors. Intriguingly, N9 cells exposed to nanoplastics exhibited substantial increases in iNOS mRNA. This effect was entirely prevented by pre-exposure to TLR4 or p38 in-hibitors, while TNF-alpha mRNA levels remained relatively stable. These findings underscore the potential of nanoplastics to activate inflammatory pathways, with response kinetics varying depending on the cell type.
引用
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页数:11
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