Li Ting, Yao Zhenghong, Huang Yuxin, Li Ran, Zhang Lu, Chen Rucheng, Gu Weijia
School of Public Health, Zhejiang Chinese Medical University, Hangzhou, China.
Zhejiang International Science and Technology Cooperation Base of Air Pollution and Health, Hangzhou, China.
FASEB J. 2025 Sep 15;39(17):e70980. doi: 10.1096/fj.202500910RR.
Microplastics (MPs), particles under 5 mm, are widespread environmental contaminants. Polystyrene (PS), used in many household items, degrades into polystyrene MPs (PS-MPs), which accumulate in the environment. Chronic exposure to waterborne PS-MPs was found to disrupt hepatic lipid metabolism in C57BL/6N mice through inflammatory Kupffer cell polarization and IL-17/NF-κB signaling pathways. While short-term PS-MPs exposure revealed preferential accumulation in the liver and testes, long-term exposure (9-12 weeks) induced significant increases in body fat percentage and hepatic lipid deposition independent of dietary changes. Mechanistically, chronic PS-MPs exposure promoted Kupffer cell polarization toward pro-inflammatory M1 phenotypes, accompanied by upregulated IL-17 expression and suppressed anti-inflammatory cytokines. Western blot analysis demonstrated concurrent elevation of lipid synthesis markers with reduced lipid oxidation and transport proteins. These findings established that PS-MPs accumulation drives hepatic steatosis through dual mechanisms of macrophage-mediated inflammation and impaired lipid homeostasis pathways.
微塑料(MPs)是指直径小于5毫米的颗粒,是广泛存在的环境污染物。许多家居用品中使用的聚苯乙烯(PS)会降解为聚苯乙烯微塑料(PS-MPs),并在环境中累积。研究发现,长期暴露于水中的PS-MPs会通过库普弗细胞的炎症极化和IL-17/NF-κB信号通路扰乱C57BL/6N小鼠的肝脏脂质代谢。短期暴露于PS-MPs时,其在肝脏和睾丸中优先积累,而长期暴露(9-12周)则会导致体脂百分比和肝脏脂质沉积显著增加,且与饮食变化无关。从机制上讲,长期暴露于PS-MPs会促使库普弗细胞向促炎性M1表型极化,同时IL-17表达上调,抗炎细胞因子受到抑制。蛋白质免疫印迹分析表明,脂质合成标志物同时升高,而脂质氧化和转运蛋白减少。这些发现表明,PS-MPs的积累通过巨噬细胞介导的炎症和脂质稳态途径受损的双重机制导致肝脏脂肪变性。