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Microarray Gene Profiling of Laser-Captured Cells: a New Tool to Study Atherosclerosis in Mice

机译:激光捕获细胞的微阵列基因谱分析:研究小鼠动脉粥样硬化的新工具。

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摘要

Genetically modified mice susceptible to atherosclerosis are widely used in atherosclerosis research. Although the atherosclerotic lesions in these animals show similarities to those in humans, comprehensive expression profile analysis of these lesions is limited by their very small size. In this communication, we have developed an approach to analyze global gene expression in mouse lesions by a combination of (a) laser capture microdissection (LCM) to isolate RNA from specific lesions, (b) an efficient RNA amplification method that reliably yields sufficient quantities of high quality cRNA for quantitative real-time PCR (qPCR), as well as for microarray analysis. The RNA passed multiple quality controls and the expression profile observed in lesional cells compared with the whole artery encompasses genes that are characteristic of a macrophage/foam cell population. We believe that this method represents a useful new tool for the unbiased analysis of global gene expression of specific sub-regions in atherosclerotic lesions in different rodent models.
机译:易患动脉粥样硬化的转基因小鼠被广泛用于动脉粥样硬化研究。尽管这些动物中的动脉粥样硬化病变与人类的相似,但这些病变的小尺寸限制了它们的全面表达谱分析。在本交流中,我们已经开发出一种通过结合以下方法分析小鼠病变中整体基因表达的方法:(a)激光捕获显微切割(LCM)从特定病变中分离RNA,(b)有效产生足够数量的有效RNA扩增方法高质量cRNA的定量实时PCR(qPCR)以及微阵列分析。 RNA通过了多种质量控制,与整个动脉相比,病变细胞中观察到的表达谱涵盖了巨噬细胞/泡沫细胞群体的特征基因。我们认为,该方法代表了一种有用的新工具,可用于对不同啮齿动物模型中动脉粥样硬化病变中特定子区域的全局基因表达进行无偏分析。

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