Regulation of Intestinal PYY cell function

肠道 PYY 细胞功能的调节

• 批准号: 8588919
• 负责人: Diego V Bohorquez
• 金额: $ 5.51万
• 依托单位: DUKE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-01-01 至 2014-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8588919
• 关键词: Anatomy; Appetite Regulation; Axon; Blood Circulation; Brain; Cell physiology; Cells; Data; Desire for food; Development; Diabetes Mellitus; Diffuse; Digestion; Distal; Elements; Endocrinology; Enteral; Enteric Nervous System; Enteroendocrine Cell; Evaluation; Fiber; Fluorescence Microscopy; Goals; Green Fluorescent Proteins; Growth; Hormones; Hunger; In Vitro; Insulin; Intestinal Mucosa; Intestines; Knowledge; L Cells; Laboratories; Laser Scanning Confocal Microscopy; Life; Link; Maintenance; Metabolic Diseases; Modeling; Molecular; Nerve; Nerve Endings; Neuroglia; Neurons; Nutrient; Obesity; Organoids; Outcome; Physiological; Play; Process; Public Health; RNA Interference; Regulation; Reporting; Research; Research Personnel; Role; Satiation; Signal Transduction; Small Intestines; Source; Structural Protein; Synapses; Techniques; Testing; Training; Transgenic Mice; absorption; base; detection of nutrient; enhanced green fluorescent protein; gastrointestinal; glucagon-like peptide; in vivo; interest; mouse model; neurofilament; neurotrophic factor; novel strategies; promoter; response; satisfaction; therapeutic development; therapy development; tyrosyltyrosine

DESCRIPTION (provided by applicant): Enteroendocrine cells play a key role in nutrient digestion and absorption, and are essential for normal life. The enteroendocrine L cell is of particular interest because it has the capacity to sense contents of the gut lumen and, in response, secretes several hormones. Two of those hormones are at the forefront of diabetes and obe- sity research: 1) the insulin-stimulating glucagon-like peptide 1 (GLP-1); and, 2) the satiety-inducing peptide tyrosine tyrosine (PYY). To study L cells, the applicant's laboratory has developed a transgenic mouse model in which the PYY promoter drives the expression of enhanced green fluorescent protein (GFP). Using the PYY- GFP model along with confocal laser scanning microscopy (LSCM), the applicant and his team have characterized the existence in L cells of a long (more than 50 5m) basal cytoplasmic process that resembles an axon. The long-term goal of the applicant is to understand how enteroendocrine cells, in particular the L cell, ex- change molecular information with enteric neurons to induce satiety and regulate appetite. The objective of this proposal is to determine the importance of the L cell basal process in the function of L cells, by assessing its role in PYY secretion and by characterizing the factors that regulate its growth and maintenance. The central hypothesis is that the L cell basal process is nurtured by specific signals derived from enteric glia, and functions as a pseudo-axon. The hypothesis has been formulated based on preliminary data developed by the applicant that show that L cells have an intimate relationship with elements of the enteric nervous system. The rationale is that by defining the function and regulation of basal processes new approaches can be developed to modulate hormone secretion from L cells. The central hypothesis will be tested in two specific aims: Aim 1 is to determine the effects of neurotrophic factors on the axon-like extension in L cells. The applicant will examine axonal process elongation in cultured primary L cells and in an intestinal organoid model that contains L cells. Aim 2 is to characterize the neurofilaments in L cell basal processes and define their role in PYY secretion. The applicant will use RNAi techniques to study in vitro and in vivo the neurofilaments found in L cells. Because PYY is a major satiety signal, the physical connection between the L cell and enteric neurons is ex- pected to carry important consequences for the regulation of appetite. The proposed project will provide the applicant with the required training to become an independent investigator in the field of gastrointestinal endocrinology.

描述（申请人提供）：肠内分泌细胞在营养物质的消化和吸收中起着关键作用，是正常生活所必需的。肠内分泌L细胞是特别有趣的，因为它有能力感知肠腔内的内容物，作为反应，分泌几种激素。其中两种激素处于糖尿病和肥胖研究的前沿：1)胰岛素刺激胰高血糖素样肽1 (GLP-1)；2)诱导饱腹感的肽酪氨酸酪氨酸（PYY）。为了研究L细胞，申请人的实验室开发了一种转基因小鼠模型，其中PYY启动子驱动增强型绿色荧光蛋白（GFP）的表达。使用PYY- GFP模型以及共聚焦激光扫描显微镜（LSCM），申请人和他的团队已经表征了L细胞中存在一个长（超过50米）的类似轴突的基细胞质过程。申请人的长期目标是了解肠内分泌细胞，特别是L细胞如何与肠神经元交换分子信息以诱导饱腹感和调节食欲。本提案的目的是通过评估其在PYY分泌中的作用以及通过表征调节其生长和维持的因素来确定L细胞基底过程在L细胞功能中的重要性。核心假说认为，L细胞基底突是由来自肠胶质细胞的特定信号培育的，具有伪轴突的功能。该假设是根据申请人开发的初步数据制定的，这些数据表明L细胞与肠神经系统的元素有密切的关系。其基本原理是，通过定义基础过程的功能和调节，可以开发出调节L细胞激素分泌的新方法。中心假设将在两个特定目标中进行测试：目标1是确定神经营养因子对L细胞轴突样延伸的影响。申请人将在培养的原代L细胞和含有L细胞的肠道类器官模型中检查轴突突伸长。目的2是表征L细胞基底突中的神经丝，并确定它们在PYY分泌中的作用。申请人将使用RNAi技术在体外和体内研究L细胞中的神经丝。由于PYY是一种主要的饱腹感信号，因此L细胞和肠神经元之间的物理连接有望对食欲调节产生重要影响。该项目将为申请人提供必要的培训，使其成为胃肠内分泌学领域的独立研究者。