2. Academic Validation
  3. SLC7A11 as a therapeutic target to attenuate phthalates-driven testosterone level decline in mice

SLC7A11 as a therapeutic target to attenuate phthalates-driven testosterone level decline in mice

  • J Adv Res. 2024 May 24:S2090-1232(24)00216-9. doi: 10.1016/j.jare.2024.05.026.
Yi Zhao 1,  Xue-Qi Wang 1,  Rui-Qi Liu 1,  Fu-Wei Jiang 1,  Jia-Xin Wang 1,  Ming-Shan Chen 1,  Hao Zhang 1,  Jia-Gen Cui 1,  Yuan-Hang Chang 1,  Jin-Long Li 2
Affiliations

Affiliations

  • 1 College of Veterinary Medicine, Northeast Agricultural University, Harbin 150030, PR China.
  • 2 College of Veterinary Medicine, Northeast Agricultural University, Harbin 150030, PR China; Key Laboratory of the Provincial Education Department of Heilongjiang for Common Animal Disease Prevention and Treatment, Northeast Agricultural University, Harbin 150030, PR China; Heilongjiang Key Laboratory for Laboratory Animals and Comparative Medicine, Northeast Agricultural University, Harbin 150030, PR China. Electronic address: [email protected].
PMID: 38797476 DOI: 10.1016/j.jare.2024.05.026
Abstract

Introduction: Phthalates exposure is a major public health concern due to the accumulation in the environment and associated with levels of testosterone reduction, leading to adverse pregnancy outcomes. However, the relationship between phthalate-induced testosterone level decline and Ferroptosis remains poorly defined.

Objectives: Herein, we aimed to explore the mechanisms of phthalates-induced testosterone synthesis disorder and its relationship to Ferroptosis.

Methods: We conducted validated experiments in vivo male mice model and in vitro mouse Leydig TM3 cell line, followed by RNA sequencing and metabolomic analysis. We evaluated the levels of testosterone synthesis-associated enzymes and ferroptosis-related indicators by using qRT-PCR and Western blotting. Then, we analyzed the lipid peroxidation, ROS, Fe2+ levels and glutathione system to confirm the occurrence of Ferroptosis.

Results: In the present study, we used di (2-ethylhexyl) phthalate (DEHP) to identify Ferroptosis as the critical contributor to phthalate-induced testosterone level decline. It was demonstrated that DEHP caused glutathione metabolism and steroid synthesis disorders in Leydig cells. As the primary metabolite of DEHP, mono-2-ethylhexyl phthalate (MEHP) triggered testosterone synthesis disorder accompanied by a decrease in the expression of solute carri1er family 7 member 11 (SLC7A11) protein. Furthermore, MEHP synergistically induced Ferroptosis with Erastin through the increase of intracellular and mitochondrial ROS, and lipid peroxidation production. Mechanistically, overexpression of SLC7A11 counteracts the synergistic effect of co-exposure to MEHP-Erastin.

Conclusion: Our research results suggest that MEHP does not induce Ferroptosis but synergizes Erastin-induced Ferroptosis. These findings provide evidence for the role of Ferroptosis in phthalates-induced testosterone synthesis disorder and point to SLC7A11 as a potential target for male reproductive diseases. This study established a correlation between Ferroptosis and phthalates cytotoxicity, providing a novel view point for mitigating the issue of male reproductive disease and "The Global Plastic Toxicity Debt".

Keywords

Di (2-ethylhexyl) phthalate; Ferroptosis; Male mice; Solute carrier family 7 member 11; Testosterone.

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