Department of Environmental and Occupational Health, West China School of Public Health, Sichuan University, Chengdu, 610041, Sichuan, China.
Biol Trace Elem Res. 2024 Mar;202(3):885-899. doi: 10.1007/s12011-023-03728-7. Epub 2023 Jun 13.
YTH N-methyladenosine RNA binding protein 2 (YTHDF2) undergoes phase separation in response to the stimulation of high concentration of arsenite, suggesting that oxidative stress, the major mechanism of arsenite toxicity, may play a role in YTHDF2 phase separation. However, whether arsenite-induced oxidative stress is involved in phase separation of YTHDF2 has yet to be established. To explore the effect of arsenite-induced oxidative stress on YTHDF2 phase separation, the levels of oxidative stress, YTHDF2 phase separation, and N-methyladenosine (mA) in human keratinocytes were detected after exposure to various concentrations of sodium arsenite (0-500 µM; 1 h) and antioxidant N-acetylcysteine (0-10 mM; 2 h). We found that arsenite promoted oxidative stress and YTHDF2 phase separation in a concentration-dependent manner. In contrast, pretreatment with N-acetylcysteine significantly relieved arsenate-induced oxidative stress and inhibited YTHDF2 phase separation. As one of the key factors to YTHDF2 phase separation, N-methyladenosine (mA) levels in human keratinocytes were significantly increased after arsenite exposure, accompanied by upregulation of mA methylesterase levels and downregulation of mA demethylases levels. On the contrary, N-acetylcysteine mitigated the arsenite-induced increase of mA and mA methylesterase and the arsenite-induced decrease in mA demethylase. Collectively, our study firstly revealed that oxidative stress induced by arsenite plays an important role in YTHDF2 phase separation driven by mA modification, which provides new insights into the arsenite toxicity from the phase-separation perspective.
YTH N-甲基腺苷 RNA 结合蛋白 2(YTHDF2)在受到高浓度亚砷酸盐刺激时会发生相分离,这表明亚砷酸盐毒性的主要机制——氧化应激可能在 YTHDF2 相分离中起作用。然而,亚砷酸盐诱导的氧化应激是否参与 YTHDF2 的相分离尚未确定。为了探讨亚砷酸盐诱导的氧化应激对 YTHDF2 相分离的影响,本研究检测了人角质形成细胞在暴露于不同浓度的亚砷酸钠(0-500 µM;1 h)和抗氧化剂 N-乙酰半胱氨酸(0-10 mM;2 h)后氧化应激、YTHDF2 相分离和 N-甲基腺苷(mA)的水平。结果发现,亚砷酸盐以浓度依赖的方式促进氧化应激和 YTHDF2 相分离。相比之下,N-乙酰半胱氨酸预处理可显著减轻亚砷酸盐诱导的氧化应激并抑制 YTHDF2 相分离。作为 YTHDF2 相分离的关键因素之一,人角质形成细胞中的 N-甲基腺苷(mA)水平在亚砷酸盐暴露后显著增加,同时 mA 甲基转移酶水平上调,mA 去甲基酶水平下调。相反,N-乙酰半胱氨酸减轻了亚砷酸盐诱导的 mA 和 mA 甲基转移酶增加以及 mA 去甲基酶减少。总之,本研究首次揭示了亚砷酸盐诱导的氧化应激在 mA 修饰驱动的 YTHDF2 相分离中起重要作用,从相分离的角度为亚砷酸盐毒性提供了新的见解。