Methylmercury induced ferroptosis by interference of iron homeostasis and glutathione metabolism in CTX cells

• Published in: Environmental pollution (1987) 2023-10, Vol.335, p.122278, Article 122278
• Main Authors: Xu, Xi, Wang, Su-Su, Zhang, Lin, Lu, An-Xin, Lin, Yin, Liu, Jun-Xia, Yan, Chong-Huai
• Format: Article
• Language: English
• Subjects: Ferroptosis; Glutathione synthesis; Iron hemostasis; Methylmercury; Nrf2
• ISSN: 0269-7491; 1873-6424; 1873-6424
• DOI: 10.1016/j.envpol.2023.122278

Environmental methylmercury (MeHg) exposure has gained global attention owing to its serious health hazards, especially neurotoxicity. Ferroptosis is a novel form of programmed cell death characterized by lipid peroxidation and iron overload. However, the occurrence of ferroptosis and its underlying mechanisms have not been fully elucidated in the methylmercury-induced neurotoxicity and the role of Nrf2 in MeHg-induced ferroptosis remains unexplored. In this study, we verified that MeHg decreased cell viability in a dose- and time-dependent manner in the Rat Brain Astrocytes cells (CTX cells). MeHg (3.5 μmol/L) exposure induced CTX cells to undergo ferroptosis, as evidenced by glutathione (GSH) depletion, lipid peroxidation, and iron overload, which was significantly rescued by the ferroptosis-specific inhibitors Ferrostatin-1 and Deferoxamine. MeHg directly disrupted the process of GSH metabolism by downregulating of SLC7A11 and GPX4 and interfered with intracellular iron homeostasis through inhibition of iron storage and export. Simultaneously, the expression of Nrf2 was upregulated by MeHg in CTX cells. Hence, the inhibition of Nrf2 activity further downregulated the levels of GPX4, SLC7A11, FTH1, and SLC40A1, which aggravated MeHg-induced ferroptosis to a greater extent. Overall, our findings provided evidence that ferroptosis played a critical role in MeHg-induced neurotoxicity, and suppressing Nrf2 activity further exacerbated MeHg-induced ferroptosis in CTX cells. [Display omitted] •1.MeHg exposure triggered ferroptosis in rat astrocytes.•2.MeHg exposure disrupted GSH metabolism by suppressing GPX4 and SLC7A11 activity.•3.MeHg exposure caused iron overload by inhibition of iron storage and export.•4.Inhibition of Nrf2 activity exacerbates MeHg-induced ferroptosis.