Liquor Marking Biological Technology and Application of Key Laboratory of Sichuan Province, College of Bioengineering, Sichuan University of Science & Engineering, Yibin, China.
Hubei Key Laboratory of Genetic Regulation and Integrative Biology, School of Life Sciences, Central China Normal University, Hubei, China.
Reprod Toxicol. 2022 Jun;110:180-187. doi: 10.1016/j.reprotox.2022.04.008. Epub 2022 Apr 26.
Dibutyl phthalate (DBP) is an environmental hormone disrupter. This study was designed to investigate whether DBP adsorbed in multi-walled carbon nanotubes (MWCNTs) can easily cross the blood-testis barrier and slow down the degradation of DBP in male mice, thereby prolonging the interference effect of DBP. The results showed that: in male Balb/C mice, the sperm density of the MWCNTs group and the DBP plus MWCNTs group decreased significantly (p < 0.05); and the sperm deformity rate increased significantly (p < 0.05). Testicular tissue sections from the combined exposure group showed that most of the seminiferous tubules were atrophied, there were more large gaps between the cells in the tubules, and the number of mature-sperm decreased. The reactive oxygen species (ROS) levels increased significantly in the combined exposure group (p < 0.01). Proteomics results showed that there were 231 differentially expressed proteins in the combined exposure group compared with the MWCNTs only group, and 69 differentially expressed proteins compared with the DBP group. GO enrichment analysis showed that the differentially expressed proteins mainly include: 60 s acid ribosomal protein P1; nuclear autoantigen sperm protein; centromere protein V; and other proteins related to cell division. These results indicate that MWCNTs with adsorbed DBP can increase oxidative damage in the testis of male mice, interfere with DNA replication and cell division in testicular tissue cells, induce cell apoptosis, and destroy the normal spermatogenic function of the testis.
邻苯二甲酸二丁酯(DBP)是一种环境激素干扰物。本研究旨在探讨吸附在多壁碳纳米管(MWCNTs)上的 DBP 是否容易穿过血睾屏障,并减缓 DBP 在雄性小鼠体内的降解速度,从而延长 DBP 的干扰作用。结果表明:在雄性 Balb/C 小鼠中,MWCNTs 组和 DBP+MWCNTs 组的精子密度明显降低(p<0.05);精子畸形率明显升高(p<0.05)。联合暴露组的睾丸组织切片显示,大多数曲细精管萎缩,管内细胞之间的大间隙增多,成熟精子数量减少。联合暴露组的活性氧(ROS)水平显著升高(p<0.01)。蛋白质组学结果显示,与 MWCNTs 组相比,联合暴露组有 231 个差异表达蛋白,与 DBP 组相比有 69 个差异表达蛋白。GO 富集分析表明,差异表达蛋白主要包括:60s 酸性核糖体蛋白 P1;核自身抗原精子蛋白;着丝粒蛋白 V;和其他与细胞分裂相关的蛋白质。这些结果表明,吸附 DBP 的 MWCNTs 可增加雄性小鼠睾丸的氧化损伤,干扰睾丸组织细胞中的 DNA 复制和细胞分裂,诱导细胞凋亡,破坏睾丸的正常生精功能。