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Effects of valproic acid on gene expression during human embryonic stem cell differentiation into neurons

机译:丙戊酸对人胚胎干细胞向神经元分化过程中基因表达的影响

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The widely used antiepileptic drug valproic acid (VPA) is known to exhibit teratogenicity in the form of a failure of the neural tube in humans. Embryonic stem cells (ESCs) are reported to be a promising cell source for evaluating chemical teratogenicity, because they are capable of reproducing embryonic developmental model and enable reduction in the number of experimental animals used. We previously investigated 22 genes for which expressions are altered by teratogens, specifically focusing on neural differentiation of mouse ESCs. In the present study, expressions of the investigated genes were evaluated by quantitative real-time PCR and compared during differentiation of human ESCs into neurons with or without VPA. Under the conditions, almost all gene expressions significantly changed in VPA-containing culture. Specifically, in neural development-related genes such as DCX, ARX, MAP2, and NNAT, more than 2-fold expression was observed. The findings suggest that the genes focused on in this study may help to elucidate the teratogenic effects of VPA and might be a useful tool to analyze embryotoxic potential of chemicals in humans.
机译:众所周知,广泛使用的抗癫痫药丙戊酸(VPA)以人类神经管衰竭的形式表现出致畸性。据报道,胚胎干细胞(ESC)是用于评估化学致畸性的有前途的细胞来源,因为它们能够复制胚胎发育模型并能够减少所用实验动物的数量。我们先前调查了22种基因,这些基因的表达被致畸物改变,特别是专注于小鼠ESC的神经分化。在本研究中,通过定量实时PCR评估所研究基因的表达,并在将人类ESC分化为有或没有VPA的神经元过程中进行比较。在这种条件下,几乎所有基因表达在含VPA的培养物中均发生了显着变化。具体而言,在与神经发育相关的基因(例如DCX,ARX,MAP2和NNAT)中,观察到2倍以上的表达。这些发现表明,本研究中关注的基因可能有助于阐明VPA的致畸作用,并且可能是分析化学物质对人类的潜在毒性的有用工具。

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