Department of Neurosciences, University of New Mexico School of Medicine, Albuquerque, New Mexico, United States of America.
PLoS One. 2013 Sep 11;8(9):e73788. doi: 10.1371/journal.pone.0073788. eCollection 2013.
Prenatal alcohol exposure can lead to fetal alcohol spectrum disorder (FASD) and associated behavioral impairments that may be linked to disruptions in adult hippocampal neurogenesis. Social and physical enrichment has been proposed as a potential therapeutic approach toward reversing behavioral deficits associated with FASD and is also a potent stimulator of adult hippocampal neurogenesis. In the present study, we utilized a genetic fate mapping approach in nestin-CreER(T2)/YFP bitransgenic mice to identify the stage-specific impact of prenatal alcohol exposure on the stepwise maturation of adult hippocampal progenitors. Using a limited alcohol access "drinking-in-the-dark" model of FASD, we confirm previous findings that moderate prenatal alcohol exposure has no effect on adult neurogenesis under standard housing conditions, but abolishes the neurogenic response to enriched environment (EE). Furthermore, we demonstrate that this effect is primarily due to failed EE-mediated survival of postmitotic neurons. Finally, we demonstrate that the neurogenic deficit is associated with impaired spatial pattern recognition, as demonstrated by delayed learning of FASD-EE mice in an A-B contextual discrimination task. These results identify a potential maturational stage-specific mechanism(s) underlying impaired neurogenic function in a preclinical model of FASD, and provide a basis for testing regulatory pathways in this model through conditional and inducible manipulation of gene expression in the adult hippocampal progenitor population.
产前酒精暴露可导致胎儿酒精谱系障碍(FASD)和相关的行为障碍,这些障碍可能与成年海马神经发生的中断有关。社会和身体丰富化被提议作为一种潜在的治疗方法,以逆转与 FASD 相关的行为缺陷,并且也是成年海马神经发生的有效刺激物。在本研究中,我们利用巢蛋白-CreER(T2)/YFP 双转基因小鼠中的遗传命运图谱方法来确定产前酒精暴露对成年海马祖细胞逐步成熟的特定阶段的影响。使用有限的酒精摄入“暗饮”FASD 模型,我们证实了先前的发现,即适度的产前酒精暴露在标准饲养条件下对成年神经发生没有影响,但消除了丰富环境(EE)对神经发生的反应。此外,我们证明这种效应主要是由于 EE 介导的有丝分裂后神经元的存活失败所致。最后,我们证明神经发生缺陷与空间模式识别受损有关,这表现为 FASD-EE 小鼠在 A-B 上下文辨别任务中的学习延迟。这些结果确定了 FASD 临床前模型中神经发生功能受损的潜在发育阶段特异性机制,并为通过在成年海马祖细胞群体中条件和诱导性地操纵基因表达来测试该模型中的调节途径提供了基础。