Behavioral Neuroscience Branch, IRP/NIDA/NIH/DHHS, 251 Bayview Boulevard, Baltimore, MD 21224, USA.
J Neurosci Methods. 2012 Jan 15;203(1):10-8. doi: 10.1016/j.jneumeth.2011.08.045. Epub 2011 Sep 3.
Molecular analysis of brain tissue is greatly complicated by having many different classes of neurons and glia interspersed throughout the brain. Fluorescence-activated cell sorting (FACS) has been used to purify selected cell types from brain tissue. However, its use has been limited to brain tissue from embryos or transgenic mice with promoter-driven reporter genes. To overcome these limitations, we developed a FACS procedure for dissociating intact cell bodies from adult wild-type rat brains and sorting them using commercially available antibodies against intracellular and extracellular proteins. As an example, we isolated neurons using a NeuN antibody and confirmed their identity using microarray and real time PCR of mRNA from the sorted cells. Our FACS procedure allows rapid, high-throughput, quantitative assays of molecular alterations in identified cell types with widespread applications in neuroscience.
脑组织的分子分析由于存在许多不同类型的神经元和神经胶质细胞而变得非常复杂,这些细胞散布在整个大脑中。荧光激活细胞分选(FACS)已被用于从脑组织中纯化选定的细胞类型。然而,它的使用仅限于来自胚胎或具有启动子驱动报告基因的转基因小鼠的脑组织。为了克服这些限制,我们开发了一种 FACS 程序,用于从成年野生型大鼠脑中分离完整的细胞体,并使用针对细胞内和细胞外蛋白的商业可得抗体对其进行分选。例如,我们使用 NeuN 抗体分离神经元,并使用从分选细胞中提取的 mRNA 的微阵列和实时 PCR 来确认其身份。我们的 FACS 程序允许快速、高通量、定量分析鉴定细胞类型中的分子变化,在神经科学中有广泛的应用。