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Comparison of gene expression signature between nascent Lhx6-GFP+ cells from mouse embryonic brain and differentiated Lhx6-GFP+ cells from ES cells (as well as comparing those of Lhx6-GFP+ and Lhx6-GFP- cells from ES cells). Mus musculus

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下载链接:
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA186616
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There was a remarkable similarity in the molecular properties of the MGE-GFP+ and ES-GFP+ cells. In particular, genes that are important for medial ganglionic eminence (MGE) and cortical interneurons development are both high in expression in both MGE-Lhx6-GFP+ and ES-Lhx6-GFP+ cells (compared to ES-Lhx6-GFP- cells). Overall design: To investigate how closely ES cells-derived Lhx6-GFP+ cells resembled authentic Lhx6+ MGE cells, and to define the molecular properties of the Lhx6-GFP+ and Lhx6-GFP- cells from differentiated ES cells, we compared their gene expression profiles. We used FACS to purify GFP+ cells from the E12.5 MGE of Lhx6-GFP transgenic mice. ES-Lhx6-GFP+ cells and ES-Lhx6-GFP- cells (both from D12 EB aggregates) were also isolated by fluorescent activated cell sorting (FACS) and all of the RNA samples were subjected to RNA expression microarray analyses.

MGE-GFP+细胞与ES-GFP+细胞的分子特性具有显著相似性。特别值得注意的是,对内侧神经节隆起(medial ganglionic eminence, MGE)及皮层中间神经元发育至关重要的基因,在MGE-Lhx6-GFP+与ES-Lhx6-GFP+细胞中均呈高表达(相较于ES-Lhx6-GFP-细胞)。实验总体设计:为探究胚胎干细胞(embryonic stem, ES)来源的Lhx6-GFP+细胞与天然Lhx6+ MGE细胞的相似程度,并明确分化所得ES细胞中Lhx6-GFP+与Lhx6-GFP-细胞的分子特性,我们对二者的基因表达谱进行了比较分析。我们采用荧光激活细胞分选(fluorescence activated cell sorting, FACS)技术,从Lhx6-GFP转基因小鼠的E12.5龄内侧神经节隆起组织中纯化得到GFP+细胞。同时,我们亦通过FACS分离得到源自D12胚体(embryoid body, EB)聚集物的ES-Lhx6-GFP+细胞与ES-Lhx6-GFP-细胞;所有RNA样本均进行了RNA表达微阵列分析。
创建时间:
2013-01-15
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