The transcriptomes, connections and development of submucosal neuron classes in the mouse small intestine

IF 21.2 1区 医学 Q1 NEUROSCIENCES
Wei Li, Khomgrit Morarach, Ziwei Liu, Sanghita Banerjee, Yanan Chen, Ashley L. Harb, Joel M. Kosareff, Charles R. Hall, Fernando López-Redondo, Elham Jalalvand, Suad H. Mohamed, Anastassia Mikhailova, David R. Linden, Ulrika Marklund
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Abstract

The enteric submucosal plexus regulates essential digestive functions, yet its neuronal composition remains incompletely understood. We identified two putative secretomotor neuron classes and a previously unrecognized submucosal intrinsic primary afferent neuron class through single-cell RNA sequencing in the mouse small intestine. Using viral-mediated labeling of each class, we uncovered their morphologies and neural projections in the submucosa–mucosa context, finding connections among all classes and an unexpected close association with enterochromaffin cells. Further transcriptome analysis at the postnatal stage and lineage tracing revealed that neuron identities in the submucosal plexus emerge through an initial binary fate split at neurogenesis, followed by phenotypic diversification, akin to the developmental process of the myenteric plexus. We propose a unified developmental framework for neuronal diversification across the gut wall. Our study offers comprehensive molecular, developmental and morphological insights into submucosal neurons, opening new avenues for exploring physiological functions, circuit dynamics and formation of the submucosal plexus.

Abstract Image

小鼠小肠粘膜下神经元类别的转录组、连接和发育
肠粘膜下神经丛调节基本的消化功能,但其神经元组成仍不完全了解。我们通过小鼠小肠的单细胞RNA测序鉴定了两种假定的分泌运动神经元类别和一种以前未被识别的粘膜下固有初级传入神经元类别。利用病毒介导的每一类标记,我们揭示了它们在粘膜下-粘膜背景下的形态和神经投射,发现了所有类别之间的联系以及与肠嗜铬细胞意想不到的密切联系。在出生后阶段进一步的转录组分析和谱系追踪显示,粘膜下神经丛中的神经元身份是通过神经发生时最初的二元命运分裂出现的,随后是表型多样化,类似于肌肠丛的发育过程。我们提出了一个统一的发展框架,神经元多样化跨越肠壁。我们的研究提供了对粘膜下神经元的分子、发育和形态学的全面了解,为探索粘膜下神经丛的生理功能、电路动力学和形成开辟了新的途径。
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来源期刊
Nature neuroscience
Nature neuroscience 医学-神经科学
CiteScore
38.60
自引率
1.20%
发文量
212
审稿时长
1 months
期刊介绍: Nature Neuroscience, a multidisciplinary journal, publishes papers of the utmost quality and significance across all realms of neuroscience. The editors welcome contributions spanning molecular, cellular, systems, and cognitive neuroscience, along with psychophysics, computational modeling, and nervous system disorders. While no area is off-limits, studies offering fundamental insights into nervous system function receive priority. The journal offers high visibility to both readers and authors, fostering interdisciplinary communication and accessibility to a broad audience. It maintains high standards of copy editing and production, rigorous peer review, rapid publication, and operates independently from academic societies and other vested interests. In addition to primary research, Nature Neuroscience features news and views, reviews, editorials, commentaries, perspectives, book reviews, and correspondence, aiming to serve as the voice of the global neuroscience community.
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