Department of Nutrition and Food Hygiene, School of Public Health, Peking University, NO.38 Xueyuan Road, Beijing, 100083, China.
Department of Nutrition and Food Hygiene, School of Public Health, Peking University, NO.38 Xueyuan Road, Beijing, 100083, China; Beijing Key Laboratory of Toxicological Research and Risk Assessment for Food Safety, Peking University, Beijing, NO.38 Xueyuan Road, Beijing, 100083, China.
Chemosphere. 2020 Sep;255:126920. doi: 10.1016/j.chemosphere.2020.126920. Epub 2020 Apr 29.
The pathological traits or diseases susceptibility caused by maternal exposure to environmental adverse insults (infection, malnutrition, environmental toxicants) could be transmitted across generations. It remains uncertain, however, whether the neurodevelopmental disturbances of offspring induced by maternal exposure to PM2.5 during early life can be inherited by subsequent generations without further exposure. In the current study, using transgenerational animal models, we found that F1 female showed poorer performance in Morris Water Maze (MWM), and the deficits in spatial learning and memory similarly presented in F2-F3 female. The transgenerationally-transmitted neurobehavioral disorders were mediated both via maternal and paternal lineage. Since the epigenetic modifications have been reported to be involved in the disturbed neurodevelopment induced by maternal exposure to detrimental environmental factors during early life, we further explored the possible epigenetic mechanism of the transgenerational effects. Intriguingly, the results displayed the significant increase in expression of Dnmt3a in F1 female offspring. And the hypermethylation of Bdnf promoter Ⅳ and downregulated expression of Bdnf in hippocampus were stably transmitted across the generations until the third generation. There was another interesting finding that the transgenerational effects were sex-specific and only emerged in female offspring. Together, our study indicated for the first time that maternal exposure to PM2.5 during early life could detrimentally affect neurobehaviors in multiple generations, and the declined expression of Bdnf induced by hypermethylation of Bdnf promoter Ⅳ mediated by Dnmts might be the potential molecular mechanism.
母体暴露于环境不良刺激(感染、营养不良、环境毒素)会导致病理特征或疾病易感性,并可跨代传递。然而,母体在生命早期暴露于 PM2.5 引起的后代神经发育障碍是否可以在没有进一步暴露的情况下遗传给后代,目前还不确定。在本研究中,我们使用了跨代动物模型,发现 F1 雌性在 Morris 水迷宫(MWM)中的表现较差,F2-F3 雌性也表现出类似的空间学习和记忆缺陷。跨代传递的神经行为障碍通过母体和父系遗传。由于已经报道了表观遗传修饰参与了母体在生命早期暴露于有害环境因素引起的神经发育障碍,我们进一步探讨了跨代效应的可能表观遗传机制。有趣的是,结果显示 F1 雌性后代中 Dnmt3a 的表达显著增加。Bdnf 启动子 IV 的高甲基化和海马中 Bdnf 的表达下调在三代中稳定传递。还有一个有趣的发现是,跨代效应具有性别特异性,仅出现在雌性后代中。总之,我们的研究首次表明,母体在生命早期暴露于 PM2.5 会对多代的神经行为产生不利影响,Bdnf 启动子 IV 的高甲基化通过 Dnmts 引起的 Bdnf 表达下降可能是潜在的分子机制。