Raihan Md Obayed, McGregor Brett A, Velaris Nathan A, Brishti Afrina, Hur Junguk, Porter James E
Department of Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, ND 58202, USA.
Methods Protoc. 2021 Dec 2;4(4):86. doi: 10.3390/mps4040086.
Microglia, the resident brain immune effectors cells, show dynamic activation level changes for most neuropsychiatric diseases, reflecting their complex regulatory function and potential as a therapeutic target. Emerging single-cell molecular biology studies are used to investigate the genetic modification of individual cells to better understand complex gene regulatory pathways. Although multiple protocols for microglia isolation from adult mice are available, it is always challenging to get sufficient purified microglia from a single brain for simultaneous DNA and RNA extraction for subsequent downstream analysis. Moreover, for data comparison between treated and untreated groups, standardized cell isolation techniques are essential to decrease variability. Here, we present a combined method of microglia isolation from a single adult mouse brain, using a magnetic bead-based column separation technique, and a column-based extraction of purified DNA-RNA from the isolated microglia for downstream application. Our current method provides step-by-step instructions accompanied by visual explanations of important steps for isolating DNA-RNA simultaneously from a highly purified microglia population.
小胶质细胞是脑内常驻的免疫效应细胞,在大多数神经精神疾病中表现出动态的激活水平变化,这反映了它们复杂的调节功能以及作为治疗靶点的潜力。新兴的单细胞分子生物学研究用于探究单个细胞的基因修饰,以更好地理解复杂的基因调控途径。虽然有多种从成年小鼠中分离小胶质细胞的方案,但要从单个大脑中获得足够纯化的小胶质细胞以同时进行DNA和RNA提取用于后续的下游分析,始终具有挑战性。此外,对于处理组和未处理组之间的数据比较,标准化的细胞分离技术对于降低变异性至关重要。在此,我们介绍一种从单个成年小鼠大脑中分离小胶质细胞的联合方法,该方法使用基于磁珠的柱分离技术,并从分离出的小胶质细胞中基于柱提取纯化的DNA-RNA用于下游应用。我们目前的方法提供了分步说明,并对从高度纯化的小胶质细胞群体中同时分离DNA-RNA的重要步骤进行了可视化解释。