Division of Genetic Medicine, Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee.
Genome Technology Access Center, McDonnell Genome Institute, St Louis, Missouri.
Gastroenterology. 2021 Feb;160(3):755-770.e26. doi: 10.1053/j.gastro.2020.09.032. Epub 2020 Sep 30.
BACKGROUND & AIMS: The enteric nervous system (ENS) coordinates essential intestinal functions through the concerted action of diverse enteric neurons (ENs). However, integrated molecular knowledge of EN subtypes is lacking. To compare human and mouse ENs, we transcriptionally profiled healthy ENS from adult humans and mice. We aimed to identify transcripts marking discrete neuron subtypes and visualize conserved EN subtypes for humans and mice in multiple bowel regions.
Human myenteric ganglia and adjacent smooth muscle were isolated by laser-capture microdissection for RNA sequencing. Ganglia-specific transcriptional profiles were identified by computationally subtracting muscle gene signatures. Nuclei from mouse myenteric neurons were isolated and subjected to single-nucleus RNA sequencing, totaling more than 4 billion reads and 25,208 neurons. Neuronal subtypes were defined using mouse single-nucleus RNA sequencing data. Comparative informatics between human and mouse data sets identified shared EN subtype markers, which were visualized in situ using hybridization chain reaction.
Several EN subtypes in the duodenum, ileum, and colon are conserved between humans and mice based on orthologous gene expression. However, some EN subtype-specific genes from mice are expressed in completely distinct morphologically defined subtypes in humans. In mice, we identified several neuronal subtypes that stably express gene modules across all intestinal segments, with graded, regional expression of 1 or more marker genes.
Our combined transcriptional profiling of human myenteric ganglia and mouse EN provides a rich foundation for developing novel intestinal therapeutics. There is congruency among some EN subtypes, but we note multiple species differences that should be carefully considered when relating findings from mouse ENS research to human gastrointestinal studies.
肠神经系统(ENS)通过各种肠神经元(ENs)的协同作用协调基本的肠道功能。然而,缺乏对 EN 亚型的综合分子认识。为了比较人和小鼠的 ENs,我们对来自成年人类和小鼠的健康 ENS 进行了转录谱分析。我们旨在确定标记离散神经元亚型的转录本,并可视化多个肠区人类和小鼠的保守 EN 亚型。
通过激光捕获显微解剖分离人肌间神经节及其相邻的平滑肌,用于 RNA 测序。通过计算减去肌肉基因特征来确定神经节特异性转录谱。从小鼠肌间神经元中分离细胞核,并进行单细胞 RNA 测序,总计超过 40 亿个读数和 25208 个神经元。使用小鼠单细胞 RNA 测序数据定义神经元亚型。在人类和小鼠数据集之间进行比较计算,确定共享的 EN 亚型标记物,并使用杂交链反应原位可视化。
基于同源基因表达,在十二指肠、回肠和结肠中,几种 EN 亚型在人类和小鼠之间是保守的。然而,一些来自小鼠的 EN 亚型特异性基因在人类中以完全不同的形态定义亚型表达。在小鼠中,我们鉴定了几个神经元亚型,这些亚型在所有肠段中稳定表达基因模块,具有 1 个或多个标记基因的梯度、区域表达。
我们对人肌间神经节和小鼠 EN 的联合转录谱分析为开发新型肠道治疗方法提供了丰富的基础。一些 EN 亚型存在一致性,但我们注意到存在多种物种差异,在将小鼠 ENS 研究的发现与人类胃肠道研究相关联时应谨慎考虑。