School of Public Health, Wuhan University, Wuhan 430071, China.
State Key Lab of Trauma and Chemical Poisoning, Key Lab of Medical Protection for Electromagnetic Radiation, Ministry of Education of China, Institute of Toxicology, College of Preventive Medicine, Army Medical University, Chongqing 400038, China; School of Public Health, China Medical University, Shenyang 110122, China.
Ecotoxicol Environ Saf. 2024 Jul 1;279:116461. doi: 10.1016/j.ecoenv.2024.116461. Epub 2024 May 19.
Polystyrene nanoplastics (PS-NPs) have been reported to accumulate in the testes and constitute a new threat to reproductive health. However, the exact effects of PS-NPs exposure on testicular cells and the underlying mechanisms remain largely unknown. The C57BL/6 male mice were orally administered with PS-NPs (80 nm) at different dosages (0, 10, and 40 mg/kg/day) for 60 days, and GC-1 cells were treated with PS-NPs in this study. Enlarged seminiferous tubule lumens and a loose and vacuolated layer of spermatogenic cells were observed in PS-NPs-exposed mice. Spermatogenic cells which may be one of the target cells for this reproductive damage, were decreased in the mice from PS-NPs group. PS-NPs caused spermatogenic cells to undergo senescence, manifested as elevated SA-β-galactosidase activity and activated senescence-related signaling p53-p21/Rb-p16 pathways, and induced cell cycle arrest. Mechanistically, Gene Ontology (GO) enrichment suggested the key role of reactive oxygen species (ROS) in PS-NPs-induced spermatogenic cell senescence, and this result was confirmed by measuring ROS levels. Moreover, ROS inhibition partially attenuated the senescence phenotype of spermatogenic cells and DNA damage. Using the male health atlas (MHA) database, Sirt1 was filtrated as the critical molecule in the regulation of testicular senescence. PS-NPs induced overexpression of the main ROS generator Nox2, downregulated Sirt1, increased p53 and acetylated p53 in vivo and in vitro, whereas these disturbances were partially restored by pterostilbene. In addition, pterostilbene intervention significantly alleviated the PS-NPs-induced spermatogenic cell senescence and attenuated ROS burst. Collectively, our study reveals that PS-NPs exposure can trigger spermatogenic cell senescence mediated by p53-p21/Rb-p16 signaling by regulating the Sirt1/ROS axis. Importantly, pterostilbene intervention may be a promising strategy to alleviate this damage.
聚苯乙烯纳米塑料 (PS-NPs) 已被报道在睾丸中积累,构成了生殖健康的新威胁。然而,PS-NPs 暴露对睾丸细胞的确切影响及其潜在机制在很大程度上仍不清楚。本研究中,将 C57BL/6 雄性小鼠经口给予不同剂量 (0、10 和 40mg/kg/天) 的 PS-NPs (80nm) 处理 60 天,并用 PS-NPs 处理 GC-1 细胞。暴露于 PS-NPs 的小鼠可见增大的生精小管管腔和疏松空泡化的精子发生细胞层。生精细胞是这种生殖损伤的靶细胞之一,在 PS-NPs 组的小鼠中减少。PS-NPs 导致精子发生细胞衰老,表现为 SA-β-半乳糖苷酶活性升高和激活与衰老相关的信号 p53-p21/Rb-p16 通路,并诱导细胞周期停滞。从机制上讲,基因本体 (GO) 富集表明活性氧 (ROS) 在 PS-NPs 诱导的精子发生细胞衰老中起关键作用,这一结果通过测量 ROS 水平得到证实。此外,ROS 抑制部分减弱了精子发生细胞的衰老表型和 DNA 损伤。使用男性健康图谱 (MHA) 数据库,筛选出 Sirt1 作为调节睾丸衰老的关键分子。PS-NPs 诱导主要的 ROS 生成酶 Nox2 过度表达,体内和体外下调 Sirt1,增加 p53 和乙酰化 p53,而 pterostilbene 部分恢复了这些紊乱。此外,pterostilbene 干预可显著缓解 PS-NPs 诱导的精子发生细胞衰老并减弱 ROS 爆发。总之,我们的研究表明,PS-NPs 暴露可通过调节 Sirt1/ROS 轴引发 p53-p21/Rb-p16 信号转导的精子发生细胞衰老。重要的是,pterostilbene 干预可能是缓解这种损伤的一种有前途的策略。