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Combined transcriptome analysis of fetal human and mouse cerebral cortex exposed to alcohol

机译:酒精接触胎儿人和小鼠大脑皮质的转录组分析

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Fetal exposure to environmental insults increases the susceptibility to late-onset neuropsychiatric disorders. Alcohol is listed as one of such prenatal environmental risk factors and known to exert devastating teratogenetic effects on the developing brain, leading to complex neurological and psychiatric symptoms observed in fetal alcohol spectrum disorder (FASD). Here, we performed a coordinated transcriptome analysis of human and mouse fetal cerebral cortices exposed to ethanol in vitro and in vivo, respectively. Up- and down-regulated genes conserved in the human and mouse models and the biological annotation of their expression profiles included many genes/terms related to neural development, such as cell proliferation, neuronal migration and differentiation, providing a reliable connection between the two species. Our data indicate that use of the combined rodent and human model systems provides an effective strategy to reveal and analyze gene expression changes inflicted by various physical and chemical environmental exposures during prenatal development. It also can potentially provide insight into the pathogenesis of environmentally caused brain disorders in humans.
机译:胎儿受到环境侮辱会增加对迟发性神经精神疾病的敏感性。酒精被列为此类产前环境危险因素之一,已知会对发育中的大脑产生破坏性的致畸作用,导致胎儿酒精谱系障碍(FASD)中观察到复杂的神经和精神症状。在这里,我们对暴露于乙醇的人和小鼠胎儿大脑皮层进行了体外转录和转录组分析。人类和小鼠模型中保守的上调和下调基因,其表达谱的生物学注释包括许多与神经发育有关的基因/术语,例如细胞增殖,神经元迁移和分化,从而为这两个物种之间提供了可靠的联系。我们的数据表明,结合使用啮齿动物模型和人类模型系统,可以提供有效的策略来揭示和分析在产前发育过程中各种物理和化学环境暴露引起的基因表达变化。它还可以潜在地洞察人类环境导致的脑部疾病的发病机理。

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