Center for Computational Toxicology and Exposure, Office of Research and Development, U.S. Environmental Protection Agency, Research Triangle Park, NC, USA.
Eurofins Discovery, Burlingame, CA, USA.
ALTEX. 2023;40(2):248–270. doi: 10.14573/altex.2203041. Epub 2022 Sep 15.
A structurally diverse set of 147 per- and polyfluoroalkyl substances (PFAS) was screened in a panel of 12 human primary cell systems by measuring 148 biomarkers relevant to (patho)physiological pathways to inform hypotheses about potential mechanistic effects of data-poor PFAS in human model systems. This analysis focused on immunosuppressive activity, which was previously reported as an in vivo effect of perfluorooctanoic acid (PFOA) and perfluorooctanesulfonic acid (PFOS), by comparing PFAS responses to four pharmacological immunosuppressants. The PFOS response profile had little correlation with reference immunosuppressants, suggesting in vivo activity does not occur by similar mechanisms. The PFOA response profile did share features with the profile of dexamethasone, although some distinct features were lacking. Other PFAS, including 2,2,3,3-tetrafluoropropyl acrylate, demonstrated more similarity to the reference immunosuppressants but with additional activities not found in the reference immunosuppressive drugs. Correlation of PFAS profiles with a database of environmental chemical responses and pharmacological probes identified potential mechanisms of bioactivity for some PFAS, including responses similar to ubiquitin ligase inhibitors, deubiquitylating enzyme (DUB) inhibitors, and thioredoxin reductase inhibitors. Approximately 21% of the 147 PFAS with confirmed sample quality were bioactive at nominal testing concentrations in the 1-60 micromolar range in these human primary cell systems. These data provide new hypotheses for mechanisms of action for a subset of PFAS and may further aid in development of a PFAS categorization strategy useful in safety assessment.
筛选了一组 12 种人类原代细胞系统,共检测了 148 种与(病理)生理途径相关的生物标志物,以研究数据不足的 PFAS 在人体模型系统中潜在的机制效应假设。该分析集中于免疫抑制活性,这是以前报道的全氟辛酸 (PFOA) 和全氟辛烷磺酸 (PFOS) 的体内效应,通过比较 PFAS 对四种药理学免疫抑制剂的反应。PFOS 的反应谱与参考免疫抑制剂相关性不大,表明体内活性不是通过类似的机制发生的。PFOA 的反应谱与地塞米松的反应谱有一些相似之处,但缺乏一些明显的特征。其他 PFAS,包括 2,2,3,3-四氟丙基丙烯酸酯,与参考免疫抑制剂的相似性更高,但具有参考免疫抑制剂中没有的额外活性。将 PFAS 谱与环境化学反应和药理学探针数据库进行相关性分析,确定了一些 PFAS 的潜在生物活性机制,包括与泛素连接酶抑制剂、去泛素化酶 (DUB) 抑制剂和硫氧还蛋白还原酶抑制剂相似的反应。在这些人类原代细胞系统中,在 1-60 微摩尔浓度范围内,147 种具有确认样本质量的 PFAS 中约有 21%具有生物活性。这些数据为 PFAS 的作用机制提供了新的假设,并可能进一步有助于开发在安全性评估中有用的 PFAS 分类策略。