Croucher Institute for Environmental Sciences, Department of Biology, Hong Kong Baptist University, Hong Kong SAR, P. R. China.
Guanxi Key Laboratory of Tumor Immunology and Microenvironmental Regulation, Guilin Medical University, Guilin, P. R. China.
Environ Sci Technol. 2020 Mar 17;54(6):3465-3475. doi: 10.1021/acs.est.0c00201. Epub 2020 Mar 6.
Perfluoroalkyl chemicals induce male reproductive toxicity. Current evidence showed the effects of the chemical exposure on the deterioration of testicular functions, and reduction in epididymal sperm counts. Previous studies showed that PFOA and PFOS displayed a high correlation with each other in seminal plasma levels, but induced different effects on semen variables. In this study, we focused on the comparative toxicity analysis of PFOA and PFOS, using a rat primary Sertoli cell model. Our transcriptomic data showed that PFOA and PFOS treatments (40 μM) perturbed global gene expression. While PFOS induced higher toxicity in affecting cytoskeleton signaling, Sertoli cell-cell junction, and inflammation, underlined by Ingenuity pathway analysis. Immunocytochemical staining revealed that PFOS treatment (40 and 80 μM) induced truncated actin filament and disorganized bundled configuration in the cell cytoplasm. Moreover, disorganized distribution of N-cadherin (N-cad) and β-catenin (β-cat), and defragmentation of ZO-1 at the Sertoli cell-cell interface was evident. At 80 μM of PFOS, cytoplasmic distribution of N-cad, β-cat, and ZO-1 were observed. We then examined whether resveratrol, a polyphenol antioxidant, was able to protect the cells from PFOS toxicity. The pretreatment of Sertoli cells with 10 μM resveratrol prevented the formation of truncated actin filament and dis-localization of β-cat. Western blot analysis showed that Res pretreatment increased the levels of basal ES proteins (N-cad and β-cat), tight junction proteins (ZO-1 and occludin), and gap junction protein, versus control.
全氟烷基化学品会导致雄性生殖毒性。现有证据表明,这种化学物质暴露会导致睾丸功能恶化,附睾精子数量减少。先前的研究表明,在精液中的水平上,PFOA 和 PFOS 之间存在高度相关性,但对精液变量的影响不同。在这项研究中,我们使用大鼠原代支持细胞模型,专注于 PFOA 和 PFOS 的比较毒性分析。我们的转录组数据显示,PFOA 和 PFOS(40 μM)处理会扰乱全局基因表达。虽然 PFOS 处理(40 和 80 μM)通过体内通路分析显示,在影响细胞骨架信号、支持细胞-细胞连接和炎症方面,引起更高的毒性。免疫细胞化学染色显示,PFOS 处理(40 和 80 μM)会诱导细胞质中截断的肌动蛋白丝和紊乱的束状结构。此外,N-钙黏蛋白(N-cad)和β-连环蛋白(β-cat)在支持细胞-细胞连接处的分布紊乱,ZO-1 断裂。在 80 μM 的 PFOS 下,细胞质中 N-cad、β-cat 和 ZO-1 的分布观察到。然后,我们检查了白藜芦醇(一种多酚抗氧化剂)是否能够保护细胞免受 PFOS 毒性的影响。Sertoli 细胞用 10 μM 白藜芦醇预处理可防止截断的肌动蛋白丝的形成和β-cat 的位置改变。Western blot 分析表明,Res 预处理增加了基础 ES 蛋白(N-cad 和 β-cat)、紧密连接蛋白(ZO-1 和 occludin)和间隙连接蛋白的水平,与对照组相比。