Glyphosate drives autophagy-dependent ferroptosis to inhibit testosterone synthesis in mouse Leydig cells

• Published in: The Science of the total environment 2024-03, Vol.914, p.169927-169927, Article 169927
• Main Authors: Lu, Lu, Lian, Cai-Yu, Lv, Yan-Ting, Zhang, Shu-Hui, Wang, Long, Wang, Lin
• Format: Article
• Language: English
• Subjects: Ferritinophagy; Ferroptosis; Glyphosate; Leydig cell; Testosterone
• ISSN: 0048-9697; 1879-1026
• DOI: 10.1016/j.scitotenv.2024.169927

Glyphosate (GLY), a widely used herbicide, can adversely affect the male reproductive health by inhibiting testosterone synthesis. Ferroptosis is a form of iron-dependent oxidative cell death that contributes to inhibition of testosterone secretion. However, it still remains unclear whether ferroptosis is involved in GLY-inhibited testosterone synthesis. Hereby, an in vitro model of 1 mM GLY-exposed testicular Leydig (TM3) cells was established to elucidate this issue. Data firstly showed that GLY causes cytotoxicity and testosterone synthesis inhibition via ferroptosis, while accumulation of lipid peroxides due to intracellular ferrous ion (Fe2+) overload and glutathione depletion is confirmed as a determinant of ferroptosis. Blockage of ferroptosis via chelation of Fe2+ or inhibition of lipid peroxidation can markedly mitigate GLY-induced testosterone synthesis inhibition. Also, autophagy activation is revealed in GLY-treated TM3 cells and nuclear receptor coactivator 4 (NCOA4)-mediated ferritinophagy is involved in ferroptosis through the release of excess Fe2+. GLY-induced cytotoxicity and testosterone synthesis inhibition are significantly alleviated by NCOA4 knockdown, demonstrating the crucial role of NCOA4-mediated ferritinophagy in GLY-inhibited testosterone synthesis. In summary, this study provides solid evidence that NCOA4-mediated ferritinophagy promotes ferroptosis to inhibit testosterone synthesis, highlighting that targeting NCOA4 may be a potential therapeutic approach in GLY-induced male reproductive toxicity. [Display omitted] •Glyphosate and ferrous ions is abbreviated as GLY and Fe2+, respectively.•GLY-triggered ferroptosis inhibits testosterone synthesis in mouse Leydig cells.•GLY-activated NCOA4-dependent ferritinophagy contributes to Fe2+ overload.•GLY-induced Fe2+ overload and glutathione depletion result in ferroptosis.