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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Genetic modification does not affect the stemness of neural stem cells in nestin promoter-GFP transgenic mice.
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Genetic modification does not affect the stemness of neural stem cells in nestin promoter-GFP transgenic mice.

机译:基因修饰不会影响Nestin启动子-GFP转基因小鼠中神经干细胞的干性。

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Because nestin promoter-GFP mice have frequently been used in neural stem cell (NSC) research, it is essential to prove that there is no alteration in the stemness of NSCs derived from this transgenic model for the interpretation and validity of the data. We compared the stemness of NSCs derived from transgenic mice expressing GFP driven by the nestin enhancer with those from wild-type (C57BL/6) mice with respect to the general gene expression profile, expression of neural stem cell markers as nestin and Sox2, and responsiveness to neurotrophins (BDNF, PDGF-BB, and NT-3). The gene expression profile analysis showed that the coefficient of correlation between the two groups was very high (r=0.9865) in the total genes. We found that 23 genes were either up- or down-regulated more than two-fold in the NSCs from the transgenic mice (p<0.05), without any obvious functional relatedness among them. Likewise, there was no difference between the two mouse groups in the expression of nestin or Sox2, the ability to form neurospheres and the neuronal differentiation of NSCs by neurotrophins. Taken together, the self-renewal and neuronal differentiation ability of NSCs from the transgenic mice showed the great similarity to those from wild-type mice. Such information will be useful when the properties of NSCs are evaluated following genetic modification in such a nestin-GFP Tg model.
机译:由于Nestin启动子-GFP小鼠已经常用于神经干细胞(NSC)研究中,因此有必要证明从该转基因模型衍生的NSC的干度没有改变,以解释数据并验证其有效性。在一般基因表达谱,神经干细胞标志物如Nestin和Sox2的表达方面,我们比较了由Nestin增强子驱动的表达GFP的转基因小鼠和野生型(C57BL / 6)小鼠的NSC的干性。对神经营养蛋白(BDNF,PDGF-BB和NT-3)的反应性。基因表达谱分析表明,在总基因中,两组之间的相关系数非常高(r = 0.9865)。我们发现,在转基因小鼠的NSC中,有23个基因上调或下调了两倍以上(p <0.05),它们之间没有明显的功能相关性。同样,两组小鼠在Nestin或Sox2的表达,形成神经球的能力以及神经营养蛋白对NSC的神经元分化方面无差异。总之,来自转基因小鼠的NSCs的自我更新和神经元分化能力与野生型小鼠的NSCs具有很大的相似性。当在这种Nestin-GFP Tg模型中进行基因修饰后评估NSC的特性时,此类信息将非常有用。

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