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首页> 外文期刊>Reproductive toxicology >Anchoring a dynamic in vitro model of human neuronal differentiation to key processes of early brain development in vivo
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Anchoring a dynamic in vitro model of human neuronal differentiation to key processes of early brain development in vivo

机译:锚定人类神经元分化的动态体外模型,对体内早期脑发育的关键过程

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摘要

We characterize temporal pathway dynamics of differentiation in an in vitro neurotoxicity model with the aim of informing design and interpretation of toxicological assays. Human neural progenitor cells (hNPCs) were cultured in differentiation conditions up to 21 days. Genes significantly changed through time were identified and grouped according to temporal dynamics. Quantitative pathway analysis identified gene ontology (GO) terms enriched among significantly changed genes and provided a temporal roadmap of pathway trends in vitro. Gene expression in hNPCs was compared with publicly available gene expression data from developing human brain tissue in vivo. Quantitative pathway analysis of significantly changed genes and targeted analysis of specific pathways of interest identified concordance between in vivo and in vitro expression associated with proliferation, migration, differentiation, synapse formation, and neurotransmission. Our analysis anchors gene expression patterns in vitro to sensitive windows of in vivo development, helping to define appropriate applications of the model.
机译:我们在体外神经毒性模型中表征了分化的时间途径动态,目的是通知毒理学测定的设计和解释。人的神经祖细胞(HNPC)在分化条件下培养至21天。根据时间动态确定并分组基因显着改变。定量途径分析鉴定了富集在显着改变的基因中的基因本体(GO)术语,并提供了体外途径趋势的时间路线图。将HNPCS中的基因表达与来自体内人类脑组织的公开可用的基因表达数据进行比较。有显着改变的基因的定量途径分析和对患者特异性途径的靶向分析,在体内和体外表达与增殖,迁移,分化,突触形成和神经递质相关的体外表达之间的一致性。我们的分析在体外锚定基因表达模式,体内开发的敏感窗口,有助于定义模型的适当应用。

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