生物
肠神经系统
电池类型
基因表达谱
回肠
细胞
单细胞分析
间质细胞
神经系统
细胞生物学
计算生物学
基因
免疫学
神经科学
遗传学
基因表达
癌症研究
内分泌学
作者
Eugene Drokhlyansky,Christopher S. Smillie,Nicholas Van Wittenberghe,Maria Ericsson,Gabriel K. Griffin,Gökçen Eraslan,Danielle Dionne,Michael S. Cuoco,Max N. Goder-Reiser,Tatyana Sharova,Olena Kuksenko,Andrew J. Aguirre,Genevieve M. Boland,Daniel B. Graham,Orit Rozenblatt–Rosen,Ramnik J. Xavier,Aviv Regev
出处
期刊:Cell
[Elsevier]
日期:2020-09-01
卷期号:182 (6): 1606-1622.e23
被引量:445
标识
DOI:10.1016/j.cell.2020.08.003
摘要
The enteric nervous system (ENS) coordinates diverse functions in the intestine but has eluded comprehensive molecular characterization because of the rarity and diversity of cells. Here we develop two methods to profile the ENS of adult mice and humans at single-cell resolution: RAISIN RNA-seq for profiling intact nuclei with ribosome-bound mRNA and MIRACL-seq for label-free enrichment of rare cell types by droplet-based profiling. The 1,187,535 nuclei in our mouse atlas include 5,068 neurons from the ileum and colon, revealing extraordinary neuron diversity. We highlight circadian expression changes in enteric neurons, show that disease-related genes are dysregulated with aging, and identify differences between the ileum and proximal/distal colon. In humans, we profile 436,202 nuclei, recovering 1,445 neurons, and identify conserved and species-specific transcriptional programs and putative neuro-epithelial, neuro-stromal, and neuro-immune interactions. The human ENS expresses risk genes for neuropathic, inflammatory, and extra-intestinal diseases, suggesting neuronal contributions to disease.
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