生物
单元格排序
纽恩
神经元
流式细胞术
转录组
基因表达
细胞生物学
人口
表型
神经科学
基因
分子生物学
遗传学
免疫组织化学
免疫学
人口学
社会学
作者
Sabina Berl,Khalad Karram,Anja Scheller,Melanie Jungblut,Frank Kirchhoff,Ari Waisman
标识
DOI:10.1016/j.jneumeth.2017.03.015
摘要
Isolation of neurons from the adult mouse CNS is important in order to study their gene expression during development or the course of different diseases.Here we present two different methods for the enrichment or isolation of neurons from adult mouse CNS. These methods: are either based on flow cytometry sorting of eYFP expressing neurons, or by depletion of non-neuronal cells by sorting with magnetic-beads.Enrichment by FACS sorting of eYFP positive neurons results in a population of 62.4% NeuN positive living neurons. qPCR data shows a 3-5fold upregulation of neuronal markers. The isolation of neurons based on depletion of non-neuronal cells using the Miltenyi Neuron Isolation Kit, reaches a purity of up to 86.5%. qPCR data of these isolated neurons shows an increase in neuronal markers and an absence of glial markers, proving pure neuronal RNA isolation.Former data related to neuronal gene expression are mainly based on histology, which does not allow for high-throughput transcriptome analysis to examine differential gene expression.These protocols can be used to study cell type specific gene expression of neurons to unravel their function in the process of damage to the CNS.
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