Mechanisms of Enteric Neuron Diversification

肠神经元多样化的机制

基本信息

批准号：
10670171
负责人：
E Michelle SOUTHARD-SMITH
金额：
$ 58.65万
依托单位：
VANDERBILT UNIVERSITY MEDICAL CENTER
依托单位国家：
美国
项目类别：
财政年份：
2021
资助国家：
美国
起止时间：
2021-08-16 至 2024-07-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/10670171
关键词：
Achalasia Address Affect Alleles Animals Biological Assay Blood flow Cell Line Cells Chick Chromatin Chronic Co-Immunoprecipitations Complement Congenital Megacolon Constipation Data Defect Development Disease Disease model Distal Embryo Enteral Enteric Nervous System Epitopes Essential Genes Event Excision Ganglia Gastrointestinal Diseases Gastrointestinal Motility Gastroparesis Gene Expression Genes Genetic Transcription Health In Situ Individual Intestinal Diseases Intestinal Motility Intestines Knowledge Lead Life Liquid substance Mediating Megacolon Motion Mus Mutant Strains Mice Mutation Neural Crest Neuroglia Neuronal Differentiation Neurons Oligodendroglia Patients Phase Play Population Proliferating Protein Isoforms Proteins Reaction Regulation Regulatory Element Repression Role Signal Pathway Small Interfering RNA Sorting Testing Transposase United States Validation Western Blotting Work antibody detection cell motility cofactor comparative design directed differentiation experimental study fetal gene interaction lentivirally transduced liquid chromatography mass spectrometry melanocyte migration motility disorder mouse model mutant nerve stem cell nervous system development neurogenesis neuron development novel therapeutics nutrient absorption progenitor regenerative segregation single-cell RNA sequencing tool transcription factor transcriptomics

项目摘要

Normal gastrointestinal (GI) motility is an essential prerequisite for nutrient absorption, fecal elimination and overall health. Nearly a quarter of the United States population is affected by intestinal disorders that lead to abnormal GI motility, chronic constipation and other functional bowel disorders. Greater understanding of the mechanisms that regulate differentiation of enteric neural progenitors (ENPs), which form the neurons and glia of the enteric nervous system (ENS), are needed to understand how the normal complement of functional enteric neurons within the intestine is generated. Sox10 is an essential transcription factor that functions in the neural crest derived progenitors that generate the ENS. Defects in Sox10 in patients and mice cause aganglionosis of the distal intestine leading to megacolon. Recent studies of Sox10 mutant mice have identified pronounced alterations of the ratios of different enteric neuron types in proximal innervated bowel of these animals that are accompanied by abnormal intestinal transit and motility. Although Sox10 is expressed in ENPs, these deficiencies among enteric neurons were unexpected because Sox10 is extinguished as neurons begin to differentiate, although its expression is sustained in enteric glia. The results suggest that Sox10 has greater roles in ENS development than simply promoting migration of ENPs during initial phases when the fetal gut is first colonized by progenitors. In the proposed analysis we will test the overarching hypothesis that Sox10 action in ENPs orchestrates transcriptional networks and chromatin accessibility setting in motion a regulatory cascade that orchestrates diversity of enteric neuron subtypes. In Aim 1 we will test the hypothesis that the mutant alleles of Sox10 alter enteric neuron ratios by disrupting transcriptional hierarchies in ENPs using single cell RNA sequencing (scRNASeq). In Aim 2 we will examine the hypothesis that Sox10 mutants disrupt chromatin accessibility in developing ENS lineages. Integration of information from these studies and validation of interacting gene effects in neural crest cultures will distinguish between potential developmental mechanisms that generate the normal repertoire of enteric neuron subtypes and will facilitate efforts to direct differentiation of enteric neurons for treatment of GI disease.

正常的胃肠道 (GI) 蠕动是营养吸收、粪便排出和整体健康的重要先决条件。近四分之一的美国人口受到肠道疾病的影响，导致胃肠道运动异常、慢性便秘和其他功能性肠道疾病。需要更好地了解肠神经祖细胞（ENP）的分化调节机制，肠神经祖细胞形成肠神经系统（ENS）的神经元和神经胶质细胞，以了解肠道内功能性肠神经元的正常补充是如何产生的。 Sox10 是一种重要的转录因子，在产生 ENS 的神经嵴衍生祖细胞中发挥作用。患者和小鼠的 Sox10 缺陷会导致远端肠道神经节缺失，从而导致巨结肠。最近对 Sox10 突变小鼠的研究发现，这些动物的近端受神经支配的肠道中不同肠神经元类型的比例发生了显着改变，并伴有异常的肠道运输和蠕动。尽管Sox10在ENP中表达，但肠神经元中的这些缺陷是出乎意料的，因为Sox10随着神经元开始分化而消失，尽管它在肠神经胶质细胞中持续表达。结果表明，在胎儿肠道首次被祖细胞定植的初始阶段，Sox10 在 ENS 发育中的作用比简单地促进 ENP 的迁移更重要。在拟议的分析中，我们将测试一个总体假设，即 ENP 中的 Sox10 作用协调转录网络和染色质可及性，从而启动调节级联，协调肠道神经元亚型的多样性。在目标 1 中，我们将使用单细胞 RNA 测序 (scRNASeq) 检验 Sox10 突变等位基因通过破坏 ENP 中的转录层次结构来改变肠神经元比例的假设。在目标 2 中，我们将检验 Sox10 突变体破坏 ENS 谱系发育过程中染色质可及性的假设。整合这些研究的信息并验证神经嵴培养物中相互作用的基因效应，将区分产生肠神经元亚型正常库的潜在发育机制，并将促进直接分化肠神经元以治疗胃肠道疾病的努力。