Chronic PFOA and PFOS exposure triggers cellular oxidative stress and alters lipid levels as revealed through multi-omics analysis

IF 6.7 Q3 ENGINEERING, ENVIRONMENTAL
Jenise Z. Paddayuman, Judith R. Cristobal, Luane J. B. Landau, Ashleigh L. Gagnon, Omer Gokcumen, Diana S. Aga and G. Ekin Atilla-Gokcumen
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Abstract

Per- and polyfluoroalkyl substances (PFAS), or “forever chemicals,” are linked to metabolic, immune, and neurotoxic disorders, yet their long-term cellular effects remain unclear. Using a 24 week chronic exposure model with non-transformed human epithelial cells, we examined responses to low, environmentally relevant concentrations of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic acid (PFOS). Integrated transcriptomic and lipidomic analyses revealed that despite minimal cellular accumulation, molecular changes emerged around week 17, marked by transcriptional signatures indicative of oxidative stress responses, cell survival pathways, and lipid metabolism. Our data suggests a multi-faceted model in which long-term PFOA and PFOS exposure induces oxidative stress mediated by SESN2 and SOD3, increases lipid biosynthesis via SREBP pathway, and causes compound-specific disruptions of membrane lipids. These findings highlight the importance of multi-omic, time-resolved approaches in uncovering the mechanisms of chronic low-dose chemical exposure and provide a foundation for future in vivo studies.

Abstract Image

通过多组学分析发现,慢性PFOA和PFOS暴露会触发细胞氧化应激并改变脂质水平。
全氟和多氟烷基物质(PFAS),或“永远的化学物质”,与代谢、免疫和神经毒性疾病有关,但它们对细胞的长期影响尚不清楚。利用非转化人类上皮细胞24周的慢性暴露模型,研究人员检测了对低环境相关浓度全氟辛酸(PFOA)和全氟辛烷磺酸(PFOS)的反应。综合转录组学和脂质组学分析显示,尽管细胞积累很少,但在第17周左右出现了分子变化,其特征是表明氧化应激反应、细胞存活途径和脂质代谢的转录特征。我们的数据表明了一个多方面的模型,在这个模型中,长期的PFOA和PFOS暴露诱导了由SESN2和SOD3介导的氧化应激,通过SREBP途径增加脂质生物合成,并导致化合物特异性的膜脂破坏。这些发现强调了多组学、时间分辨方法在揭示慢性低剂量化学物质暴露机制方面的重要性,并为未来的体内研究奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
1.90
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0.00%
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