体内
人口
体外
食品科学
生物
环境卫生
医学
生物技术
生物化学
作者
Ziyuan Li,Ze Zhang,Biao Zhang,Chengying Zhou,Hongyan Yu,Liting Xu,Zhicong He,Pu Chen,Wei Peng,Mingliang Ye,Guangbo Qu,Xiaomin Zhang,Yang Song,Xiaoting Jin,Yuxin Zheng
出处
期刊:PNAS nexus
[Oxford University Press]
日期:2025-04-30
卷期号:4 (5): pgaf153-pgaf153
被引量:1
标识
DOI:10.1093/pnasnexus/pgaf153
摘要
Abstract Perfluorinated compounds (PFCs) are a well-recognized environmental risk factor for atherosclerosis. However, corresponding atherogenic risk in susceptible populations consuming high-fat diets (HFDs) remains unclear. Here, we found that perfluorooctane sulfonic acid (PFOS), a canonical PFCs, elevated the atherogenic risk in mice fed with HFD, which was characterized by an increased number of pro-inflammatory phenotype macrophages. We also found that macrophages exhibited a metabolic reprogramming to glycolysis, which was attributed to increased intracellular Fe2+ level. Mechanistic investigation revealed that PFOS directly bound to the iron-storage site on the ferritin heavy chain, subsequently weakening the iron-storage function. Notably, PFCs with acidic substituents and short chains had a higher atherogenic risk, as evidenced in the crucial indicators and observed in a population with a high triglyceride level. These findings highlight the potential atherogenic risk posed by PFCs exposure in susceptible populations consuming HFD and provide a potential intervention target.
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