College of Veterinary Medicine, Northeast Agricultural University, Harbin 150030, PR China.
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, College of Veterinary Medicine, Northeast Agricultural University, Harbin 150030, PR China.
Sci Total Environ. 2023 May 1;871:161962. doi: 10.1016/j.scitotenv.2023.161962. Epub 2023 Feb 10.
The joint pollution of microplastics (MPs) and di-(2-ethylhexyl) phthalic acid (DEHP) often occurs, and consequently poses a serious threat to human and animal health, which has attracted widespread attention. However, the damage to the female mammalian ovary caused by the single exposure and co-exposure of MPs and DEHP and its specific mechanisms are not clear. Here, we established mouse models of single and co-exposures to polystyrene-microplastics (PS-MPs) and DEHP. The results showed that exposed to 100 mg/L PS-MPs and 200 mg/kg DEHP for 35 days destroyed the ovarian granulosa cell layer of mice, leading to follicular fragmentation and atresia. We cultured ovary granulosa cells in vitro to perform further mechanism studies and found that PS-MPs and DEHP had synergistic effects. Both of them promoted the excessive production of ROS and induced oxidative stress by triggering the CNR1/CRBN/YY1/CYP2E1 signaling axis, which in turn caused DNA oxidative damage. Additionally, we provided compelling evidence that oxidative stress mediated-hippo signaling pathway played a critical role in PS-MPs and DEHP caused ovary damage, resulting in ovarian granulosa cell cycle arrest and necroptosis. Using oxidative stress inhibitor AM251 or DAS could reverse these changes markedly and alleviate the reproductive toxicity caused by PS-MPs and DEHP, effectively. Overall, these results demonstrated that co-exposure of PS-MPs and DEHP adversely affected the integrity of ovary granulosa cell layer, resulting in DNA oxidative damage, cell cycle arrest and increased necroptosis of mouse ovarian granulosa cells by inducing oxidative stress. Our study shed new light on the co-exposure toxicity of PS-MPs and DEHP, provided novel insights for the reproductive toxicity of PS-MPs combined exposure with DEHP in female animals from a new free radical generation pathway perspective.
微塑料(MPs)和邻苯二甲酸二(2-乙基己基)酯(DEHP)的联合污染经常发生,因此对人类和动物健康构成严重威胁,这引起了广泛关注。然而,MPs 和 DEHP 的单一暴露和共暴露对雌性哺乳动物卵巢造成的损害及其具体机制尚不清楚。在这里,我们建立了 MPs 和 DEHP 单一和共暴露的小鼠模型。结果表明,暴露于 100mg/L PS-MPs 和 200mg/kg DEHP 35 天破坏了小鼠的卵巢颗粒细胞层,导致卵泡碎裂和闭锁。我们在体外培养卵巢颗粒细胞进行进一步的机制研究,发现 PS-MPs 和 DEHP 具有协同作用。它们都通过触发 CNR1/CRBN/YY1/CYP2E1 信号轴促进 ROS 的过度产生和诱导氧化应激,进而导致 DNA 氧化损伤。此外,我们提供了令人信服的证据表明,氧化应激介导的 Hippo 信号通路在 PS-MPs 和 DEHP 引起的卵巢损伤中起着关键作用,导致卵巢颗粒细胞周期停滞和坏死性凋亡。使用氧化应激抑制剂 AM251 或 DAS 可以显著逆转这些变化,并有效减轻 PS-MPs 和 DEHP 引起的生殖毒性。总的来说,这些结果表明,PS-MPs 和 DEHP 的共暴露会对卵巢颗粒细胞层的完整性产生不利影响,导致 DNA 氧化损伤、细胞周期停滞和小鼠卵巢颗粒细胞坏死性凋亡增加,从而诱导氧化应激。我们的研究为 PS-MPs 和 DEHP 的共暴露毒性提供了新的认识,并从新的自由基生成途径为 PS-MPs 与 DEHP 联合暴露对雌性动物生殖毒性提供了新的见解。