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高通量鉴定促进小鼠胚胎干细胞神经元形成和谱系选择的基因。

High-throughput identification of genes promoting neuron formation and lineage choice in mouse embryonic stem cells.

作者信息

Falk Anna, Karlsson Tobias E, Kurdija Sanja, Frisén Jonas, Zupicich Joel

机构信息

Karolinska Institute, Cell and Developmental Biology, Box 285, Stockholm 17177, Sweden.

出版信息

Stem Cells. 2007 Jun;25(6):1539-45. doi: 10.1634/stemcells.2006-0485. Epub 2007 Mar 22.

Abstract

The potential of embryonic stem cells to differentiate to all cell types makes them an attractive model for development and a potential source of cells for transplantation therapies. Candidate approaches have identified individual genes and proteins that promote the differentiation of embryonic stem cells to desired fates. Here, we describe a rapid large-scale screening strategy for the identification of genes that influence the pluripotency and differentiation of embryonic stem cells to specific fates, and we use this approach to identify genes that induce neuron formation. The power of the strategy is validated by the fact that, of the 15 genes that resulted in the largest increase in neuron number, 8 have previously been implicated in neuronal differentiation or survival, whereas 7 represent novel genes or known genes not previously implicated in neuronal development. This is a simple, fast, and generally applicable strategy for the identification of genes promoting the formation of any specific cell type from embryonic stem cells. Disclosure of potential conflicts of interest is found at the end of this article.

摘要

胚胎干细胞分化为所有细胞类型的潜能使其成为发育研究的一个有吸引力的模型,以及移植治疗细胞的一个潜在来源。候选方法已鉴定出促进胚胎干细胞向所需命运分化的单个基因和蛋白质。在此,我们描述了一种快速大规模筛选策略,用于鉴定影响胚胎干细胞多能性和向特定命运分化的基因,并且我们使用这种方法来鉴定诱导神经元形成的基因。该策略的有效性通过以下事实得到验证:在导致神经元数量增加最多的15个基因中,有8个先前已被证明与神经元分化或存活有关,而另外7个代表新基因或先前未涉及神经元发育的已知基因。这是一种简单、快速且普遍适用的策略,用于鉴定促进胚胎干细胞形成任何特定细胞类型的基因。潜在利益冲突的披露见本文末尾。

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