Sheffield Institute for Translational Neuroscience, The University of Sheffield, 385A Glossop Road, Sheffield, UK.
J Neurosci Methods. 2012 Jul 15;208(2):108-13. doi: 10.1016/j.jneumeth.2012.04.014. Epub 2012 Apr 26.
Isolating individual populations of cells from post-mortem (PM) central nervous system (CNS) tissue for transcriptomic analysis will provide important insights into the pathogenesis of neurodegenerative diseases. To date, research on individual CNS cell populations has been hindered by the availability of suitable PM material, unreliable sample preparation and difficulties obtaining individual cell populations. In this paper we report how rapid immunohistochemistry combined with laser capture microdissection (immuno-LCM) enables the isolation of specific cell populations from PM CNS tissue, thereby enabling the RNA profile of these individual cell types to be investigated. Specifically, we detail methods for isolating enriched glial populations (astrocytes, oligodendrocytes and microglia) and confirm this cell enrichment by polymerase chain reaction (PCR). In addition, the study details the numbers of each glial population required to obtain 50ng RNA, a suitable amount of starting material required to carry out microarray analysis that potentially may identify alterations of cell-specific genes and pathways associated with a range of neurodegenerative disorders.
从死后(PM)中枢神经系统(CNS)组织中分离单个细胞群体进行转录组分析,将为神经退行性疾病的发病机制提供重要的见解。迄今为止,对单个中枢神经系统细胞群体的研究受到合适的 PM 材料、不可靠的样品制备和难以获得单个细胞群体的限制。在本文中,我们报告了如何通过快速免疫组织化学结合激光捕获显微切割(immuno-LCM)从 PM CNS 组织中分离特定的细胞群体,从而能够研究这些单个细胞类型的 RNA 谱。具体来说,我们详细介绍了从富含神经胶质的细胞群体(星形胶质细胞、少突胶质细胞和小胶质细胞)中分离的方法,并通过聚合酶链反应(PCR)确认了这种细胞的富集。此外,该研究还详细说明了获得 50ng RNA 所需的每种神经胶质细胞群体的数量,这是进行微阵列分析所需的合适起始材料量,该分析可能会鉴定与一系列神经退行性疾病相关的特定基因和途径的改变。