Department of Occupational and Environmental Health, School of Public Health, Guangxi Medical University, Nanning, Guangxi 530021, China.
Southern Laboratory of Ocean Science and Engineering, School of Civil Engineering, Sun Yat-Sen University, Zhuhai 519000, China.
Ecotoxicol Environ Saf. 2023 Jun 1;257:114926. doi: 10.1016/j.ecoenv.2023.114926. Epub 2023 Apr 23.
Iodoacetic acid (IAA) is an emerging and the most genotoxic iodinated disinfection byproduct to date. IAA can disrupt the thyroid endocrine function in vivo and in vitro, but the underlying mechanisms remain unclear. In this work, transcriptome sequencing was used to investigate the effect of IAA on the cellular pathways of human thyroid follicular epithelial cell line Nthy-ori 3-1 and determine the mechanism of IAA on the synthesis and secretion of thyroid hormone (TH) in Nthy-ori 3-1 cells. Results of transcriptome sequencing indicated that IAA affected the TH synthesis pathway in Nthy-ori 3-1 cells. IAA reduced the mRNA expression of thyroid stimulating hormone receptor, sodium iodide symporter, thyroid peroxidase, thyroglobulin, paired box 8 and thyroid transcription factor-2, inhibited the cAMP/PKA pathway and Na-K-ATPase, and decreased the iodine intake. The results were confirmed by our previous findings in vivo. Additionally, IAA downregulated glutathione and the mRNA expression of glutathione peroxidase 1, leading to increased reactive oxygen species production. This study is the first to elucidate the mechanisms of IAA on TH synthesis in vitro. The mechanisms are associated with down-regulating the expression of genes related to TH synthesis, inhibiting iodine uptake, and inducing oxidative stress. These findings may improve future health risk assessment of IAA on thyroid in human.
碘乙酸(IAA)是一种新兴的且具有最强遗传毒性的碘化消毒副产物。IAA 可以在体内和体外破坏甲状腺内分泌功能,但潜在机制尚不清楚。在这项工作中,我们使用转录组测序来研究 IAA 对人甲状腺滤泡上皮细胞系 Nthy-ori 3-1 细胞通路的影响,并确定 IAA 对 Nthy-ori 3-1 细胞中甲状腺激素(TH)合成和分泌的作用机制。转录组测序的结果表明,IAA 影响了 Nthy-ori 3-1 细胞中的 TH 合成途径。IAA 降低了甲状腺刺激激素受体、钠碘同向转运体、甲状腺过氧化物酶、甲状腺球蛋白、配对盒 8 和甲状腺转录因子-2 的 mRNA 表达,抑制了 cAMP/PKA 通路和 Na-K-ATP 酶,并减少了碘的摄入。这些结果得到了我们之前体内研究的证实。此外,IAA 下调了谷胱甘肽和谷胱甘肽过氧化物酶 1 的 mRNA 表达,导致活性氧产生增加。本研究首次阐明了 IAA 体外对 TH 合成的作用机制。这些机制与下调与 TH 合成相关的基因表达、抑制碘摄取和诱导氧化应激有关。这些发现可能有助于未来对人类甲状腺中 IAA 的健康风险评估。