Development and Homeostasis of the Nervous System Laboratory, The Francis Crick Institute, London, UK.
Department of Immunology, Department of Neuroscience, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Nat Protoc. 2022 Aug;17(8):1789-1817. doi: 10.1038/s41596-022-00697-4. Epub 2022 Jun 8.
The enteric nervous system (ENS) is an extensive network of enteric neurons and glial cells that is intrinsic to the gut wall and regulates almost all aspects of intestinal physiology. While considerable advancement has been made in understanding the genetic programs regulating ENS development, there is limited understanding of the molecular pathways that control ENS function in adult stages. One of the limitations in advancing the molecular characterization of the adult ENS relates to technical difficulties in purifying healthy neurons and glia from adult intestinal tissues. To overcome this, we developed novel methods for performing transcriptomic analysis of enteric neurons and glia, which are based on the isolation of fluorescently labeled nuclei. Here we provide a step-by-step protocol for the labeling of adult mouse enteric neuronal nuclei using adeno-associated-virus-mediated gene transfer, isolation of the labeled nuclei by fluorimetric analysis, RNA purification and nuclear RNA sequencing. This protocol has also been adapted for the isolation of enteric neuron and glia nuclei from myenteric plexus preparations from adult zebrafish intestine. Finally, we describe a method for visualization and quantification of RNA in myenteric ganglia: Spatial Integration of Granular Nuclear Signals (SIGNS). By following this protocol, it takes ~3 d to generate RNA and create cDNA libraries for nuclear RNA sequencing and 4 d to carry out high-resolution RNA expression analysis on ENS tissues.
肠神经系统(ENS)是肠道壁固有且广泛存在的肠神经元和神经胶质细胞网络,它调节着肠道生理学的几乎所有方面。尽管在理解调节 ENS 发育的遗传程序方面已经取得了相当大的进展,但对控制成年阶段 ENS 功能的分子途径的理解有限。在推进成年 ENS 的分子特征描述方面的一个限制因素与从成年肠道组织中纯化健康神经元和神经胶质的技术困难有关。为了克服这一问题,我们开发了用于对肠神经元和神经胶质进行转录组分析的新方法,这些方法基于荧光标记核的分离。在这里,我们提供了一种使用腺相关病毒介导的基因转移对成年小鼠肠神经元核进行标记的分步方案,通过荧光分析分离标记的核,RNA 纯化和核 RNA 测序。该方案也已适应于从成年斑马鱼肠道肌间神经丛制备物中分离肠神经元和神经胶质核。最后,我们描述了一种用于肌间神经节中 RNA 可视化和定量的方法:颗粒核信号的空间整合(SIGNS)。按照本方案,大约需要 3 天时间生成 RNA 并为核 RNA 测序创建 cDNA 文库,并且需要 4 天时间对 ENS 组织进行高分辨率 RNA 表达分析。