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帕金森病死后大脑中单个神经元的紫外激光显微切割及mRNA表达分析

UV-laser microdissection and mRNA expression analysis of individual neurons from postmortem Parkinson's disease brains.

作者信息

Gründemann Jan, Schlaudraff Falk, Liss Birgit

机构信息

Wolfson Institute for Biomedical Research, University College London, London, UK.

出版信息

Methods Mol Biol. 2011;755:363-74. doi: 10.1007/978-1-61779-163-5_30.

Abstract

Cell specificity of gene expression analysis is essential to avoid tissue sample related artifacts, in particular when the relative number of target cells present in the compared tissues varies dramatically, e.g., when comparing dopamine neurons in midbrain tissues from control subjects with those from Parkinson's disease (PD) cases. Here, we describe a detailed protocol that combines contact-free UV-laser microdissection and quantitative PCR of reverse-transcribed RNA of individual neurons from postmortem human midbrain tissue from PD patients and unaffected controls. Among expression changes in a variety of dopamine neuron marker, maintenance, and cell-metabolism genes, we found that α-synuclein mRNA levels were significantly elevated in individual neuromelanin-positive dopamine midbrain neurons from PD brains when compared to those from matched controls.

摘要

基因表达分析的细胞特异性对于避免与组织样本相关的假象至关重要,特别是当比较的组织中存在的靶细胞相对数量差异很大时,例如,当比较来自对照受试者与帕金森病(PD)患者的中脑组织中的多巴胺神经元时。在这里,我们描述了一种详细的方案,该方案结合了非接触式紫外激光显微切割和对来自PD患者和未受影响对照的死后人类中脑组织中单个神经元的逆转录RNA进行定量PCR。在多种多巴胺神经元标记、维持和细胞代谢基因的表达变化中,我们发现,与匹配对照相比,来自PD大脑的单个神经黑素阳性多巴胺中脑神经元中的α-突触核蛋白mRNA水平显著升高。

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