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Secretion From Individual Vesicles

单个囊泡的分泌

基本信息

批准号：
8204506
负责人：
Robert Mark Wightman
金额：
$ 28.14万
依托单位：
UNIV OF NORTH CAROLINA CHAPEL HILL
依托单位国家：
美国
项目类别：
财政年份：
1999
资助国家：
美国
起止时间：
1999-07-01 至 2013-12-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8204506
关键词：
Adenosine Adopted Adrenal Glands Affect Back Binding Biochemical Biological Blood Vessels Brain Buffers Carrier Proteins Catecholamines Cell membrane Cells Chemicals Communication Diffusion Dopamine Electrodes Evaluation Event Excision Exocytosis Extracellular Fluid Extracellular Space Green Fluorescent Proteins Health Imagery Implant Individual Investigation Knockout Mice Laboratories Location Measurement Membrane Potentials Membrane Proteins Methods Microelectrodes Mitochondria Mitochondrial Proteins Monitor Mus Nerve Neuraxis Neuroendocrine Cell Neurons Neurosecretory Systems Neurotransmitters Physiological Play Positioning Attribute Preparation Process Production Protein Overexpression Proteins Regulation Research Role Secretory Cell Series Slice Synapsins Techniques Tissues Transgenic Mice Tyrosine 3-Monooxygenase UCP2 protein Vesicle Wild Type Mouse Work brain tissue carbon fiber chemical release dopamine transporter dopaminergic neuron extracellular neurotransmission overexpression promoter receptor

项目摘要

DESCRIPTION (provided by applicant): Chemical communication involves release of chemical messengers from biological cells, their diffusion to target cells, binding to specific receptors, and clearance from the extracellular space. Amperometry at a carbon-fiber microelectrode (with an applied potential sufficient to oxidize catecholamines) placed next to an isolated secretory cell can follow exocytosis as a series of current spikes composed of discrete packets of catecholamines detected by their electrooxidation. To evaluate events after exocytosis, carbon-fiber microelectrodes can be placed in tissue slices maintained in physiological buffer. The single cell measurements allow evaluation of individual exocytotic events while the tissue slice measurements provide key information on the diffusion and clearance of the released substances. In this proposal we set forth a plan to investigate some biochemical and physiochemical aspects that are central to chemical communication using the electrochemical approaches that we have developed. In these investigations we will probe the dynamics of release events both at single cells and in intact tissue slices. Thus, this proposal expands upon our prior work by providing a more complete view of the regulation of concentrations of chemical messengers from exocytosis to their removal from the extracellular fluid. Three specific proteins, each positioned at a central regulatory location, will be targets; for each protein, transgenically altered mice are available to us with deletions or additions of these proteins. The first is uncoupling protein 2 (UCP2), a mitochondrial protein found within neurons that is a key regulator of adenosine triphospate (ATP) production. The second is synapsin, a protein that is central to vesicular localization within nerve terminals. The third is the dopamine transporter (DAT), the protein responsible for reincorporation of dopamine back into its neurons. Thus, the specific aims of this proposal are: 1. Examine the role of UCP2, a mitochondrial protein that can diminish ATP production. We will examine its effects on neurotransmitter storage and release. 2. Examine the role of synapsin in determining the availability of vesicles for release. Synapsin, an abundant vesicular membrane protein, has been proposed to regulate the availability of vesicles for release. 3. Examine the extracellular lifetime of dopamine in the brains of mice that overexpress the DAT. We will examine the consequences of overexpression of this protein on dopaminergic neurotransmission. 4. Examine dopamine release in the brains of transgenic mice that express green-fluorescent protein (GFP) in neurons containing tyrosine hydroxylase (TH). 5. Evaluate control mechanisms of released catecholamines within the adrenal gland. Through precise placement of carbon-fiber microelectrodes within adrenal slices, we will monitor catecholamines from their exocytotic release to their transport to the blood vessels. The proposed research will provide an unprecedented view of chemical communication in the central nervous and neuroendocrine systems. PUBLIC HEALTH RELEVANCE: Chemical communication involves release of chemical messengers from biological cells, diffusion of secreted substances to target cells, binding to specific receptors, and clearance from the extracellular space. In the proposed research, these processes will be investigated with chemical sensing microelectrodes placed adjacent to isolated cells or implanted in slices of brain tissue.

描述（由申请人提供）：化学通讯涉及从生物细胞释放化学信使、扩散至靶细胞、与特定受体结合以及从细胞外间隙清除。安培在碳纤维微电极（施加的电位足以氧化儿茶酚胺）放置在旁边的一个孤立的分泌细胞可以遵循胞吐作为一系列的电流尖峰组成的离散包的儿茶酚胺检测其电氧化。为了评估胞吐后的事件，可以将碳纤维微电极放置在保持在生理缓冲液中的组织切片中。单细胞测量允许评价个体胞吐事件，而组织切片测量提供关于释放物质的扩散和清除的关键信息。在这个提案中，我们提出了一个计划，以调查一些生物化学和物理化学方面的化学通信使用的电化学方法，我们已经开发的核心。在这些调查中，我们将探讨在单细胞和完整的组织切片的释放事件的动力学。因此，这一建议扩大了我们以前的工作，提供了一个更完整的观点，从胞吐作用的化学信使的浓度的调节，他们从细胞外液中去除。三个特定的蛋白质，每个定位在一个中央调控位置，将是目标;对于每一个蛋白质，转基因改变的小鼠可供我们删除或添加这些蛋白质。第一种是解偶联蛋白2（UCP 2），这是一种在神经元中发现的线粒体蛋白，是三磷酸腺苷（ATP）产生的关键调节因子。第二种是突触蛋白，一种在神经末梢内对囊泡定位起关键作用的蛋白质。第三种是多巴胺转运蛋白（DAT），这种蛋白负责将多巴胺重新整合回神经元。因此，本提案的具体目标是：1.检查UCP 2的作用，UCP 2是一种可以减少ATP产生的线粒体蛋白。我们将研究其对神经递质储存和释放的影响。2.检查突触蛋白在决定释放囊泡的可用性中的作用。突触蛋白是一种丰富的囊泡膜蛋白，被认为可以调节囊泡的释放。3.研究过表达DAT的小鼠脑中多巴胺的细胞外寿命。我们将研究过表达这种蛋白质对多巴胺能神经传递的影响。4.检测转基因小鼠脑中多巴胺的释放，转基因小鼠在含有酪氨酸羟化酶（TH）的神经元中表达绿色荧光蛋白（GFP）。5.评估肾上腺内释放的儿茶酚胺的控制机制。通过在肾上腺切片内精确放置碳纤维微电极，我们将监测从胞吐释放到运输到血管的儿茶酚胺。这项拟议的研究将为中枢神经和神经内分泌系统中的化学通讯提供前所未有的视角。公共卫生相关性：化学通讯涉及从生物细胞释放化学信使，分泌物质扩散到靶细胞，与特定受体结合，以及从细胞外间隙清除。在拟议的研究中，这些过程将通过放置在隔离细胞附近或植入脑组织切片中的化学传感微电极进行研究。