Moreno-Campos Rodrigo, Mummaneni Nikhita S, Uribe Rosa A
Department of Biosciences, Rice University, Houston, Texas, USA.
Laboratory of Neural Crest and Enteric Nervous System Development, Rice University, Houston, Texas, USA.
FASEB J. 2025 Sep 15;39(17):e71019. doi: 10.1096/fj.202501470R.
The enteric nervous system (ENS) is the intrinsic nervous system of the gut and controls essential functions, such as gut motility, intestinal barrier function, and water balance. The ENS displays a complex 3D architecture within the context of the gut and specific transcriptional states needed to control gut homeostasis. During development, the ENS develops from enteric neural progenitor cells (ENPs) that migrate into the gut and differentiate into functionally diverse neuron types. Incorrect ENS development can disrupt ENS function and induce various gut disorders, including the congenital disease Hirschsprung disease, or various other functional gut neurological disorders, such as esophageal achalasia. In this study, we used the zebrafish larval model and performed whole gut spatial genomic analysis (SGA) of the differentiating ENS at cellular resolution. To that end, a pipeline was developed that integrated early and late developmental ENS stages by linking various spatial and transcriptional dimensions to discover regionalized cellular groups and their co-expression similarity. We identified 3D networks of intact ENS surrounding the gut and predicted cellular connectivity properties based on the stage. Spatial variable genes, such as hoxb5b, hoxa4a, etv1, and ret, were regionalized along gut axes, suggesting they may have a precise spatiotemporal control of ENS development. The application of SGA to ENS development provides new insights into its cellular transcriptional networks and interactions and provides a baseline data set to further advance our understanding of gut neurodevelopmental disorders such as Hirschsprung disease and congenital enteric neuropathies.
肠神经系统(ENS)是肠道的内在神经系统,控制着诸如肠道蠕动、肠屏障功能和水平衡等基本功能。ENS在肠道环境中呈现出复杂的三维结构以及控制肠道内环境稳定所需的特定转录状态。在发育过程中,ENS由迁移至肠道并分化为功能多样的神经元类型的肠神经祖细胞(ENP)发育而来。ENS发育异常会破坏其功能,并引发各种肠道疾病,包括先天性疾病先天性巨结肠,或其他各种功能性肠道神经疾病,如食管失弛缓症。在本研究中,我们使用斑马鱼幼体模型,以细胞分辨率对分化中的ENS进行了全肠道空间基因组分析(SGA)。为此,我们开发了一个流程,通过连接各种空间和转录维度来整合ENS发育的早期和晚期阶段,以发现区域化的细胞群及其共表达相似性。我们识别出围绕肠道的完整ENS的三维网络,并根据发育阶段预测了细胞连接特性。诸如hoxb5b、hoxa4a、etv1和ret等空间可变基因沿肠道轴区域化,这表明它们可能对ENS发育具有精确的时空控制。将SGA应用于ENS发育,为其细胞转录网络和相互作用提供了新的见解,并提供了一个基线数据集,以进一步加深我们对先天性巨结肠和先天性肠道神经病等肠道神经发育障碍的理解。