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成年小鼠大脑中动脉闭塞后室下区神经祖细胞体内和体外基因表达谱的比较。

Comparison of in vivo and in vitro gene expression profiles in subventricular zone neural progenitor cells from the adult mouse after middle cerebral artery occlusion.

作者信息

Liu X S, Zhang Z G, Zhang R L, Gregg S R, Meng H, Chopp M

机构信息

Department of Neurology, Henry Ford Health Sciences Center, Detroit, MI 48202, USA.

出版信息

Neuroscience. 2007 May 25;146(3):1053-61. doi: 10.1016/j.neuroscience.2007.02.056. Epub 2007 Apr 11.

Abstract

Stroke stimulates neurogenesis in the adult rodent brain. The molecules that mediate stroke-induced neurogenesis are not definitely known. Using microarrays containing approximately 400 known genes associated with stem cell and angiogenesis, we compared transcriptional profiles of subventricular zone (SVZ) tissue with cultured neural progenitor cells isolated from the SVZ 7 days after ischemic stroke in the adult mouse. In SVZ tissue, we found that stroke upregulated 58 genes which are involved in multiple signaling pathways during embryonic development, suggesting that stroke recaptures embryonic molecular signals. In neural progenitor cells cultured in growth medium, 23 gene expressions were increased after stroke and 8 of 23 genes overlapped with upregulated genes in stroke SVZ tissue. Expression alterations of selected genes were confirmed by real-time RT-PCR and immunohistochemistry. These in vivo and in vitro data provide new insight into the genetic program of adult SVZ neural progenitor cells after stroke and demonstrate gene expression differences between SVZ tissue and cultured SVZ cells.

摘要

中风可刺激成年啮齿动物大脑中的神经发生。介导中风诱导神经发生的分子尚不完全清楚。我们使用包含约400个与干细胞和血管生成相关的已知基因的微阵列,比较了成年小鼠缺血性中风7天后,脑室下区(SVZ)组织与从SVZ分离的培养神经祖细胞的转录谱。在SVZ组织中,我们发现中风上调了58个在胚胎发育过程中参与多种信号通路的基因,这表明中风重现了胚胎分子信号。在生长培养基中培养的神经祖细胞中,中风后23个基因表达增加,其中8个基因与中风SVZ组织中上调的基因重叠。通过实时RT-PCR和免疫组织化学证实了所选基因的表达变化。这些体内和体外数据为中风后成年SVZ神经祖细胞的遗传程序提供了新的见解,并证明了SVZ组织与培养的SVZ细胞之间的基因表达差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ae7/1942046/60e812b79cf1/nihms-23848-f0001.jpg

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Comparative analysis of in vitro conditions for rat adult neural progenitor cells.
J Neurosci Methods. 2007 Apr 15;161(2):250-8. doi: 10.1016/j.jneumeth.2006.11.012. Epub 2007 Jan 17.
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