Compartmentation of Neuronal ATP and Metabolic Regulation of Excitability

神经元 ATP 的划分和兴奋性的代谢调节

• 批准号: 8442324
• 负责人: Mathew Tantama
• 金额: $ 5.57万
• 依托单位: HARVARD MEDICAL SCHOOL
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-02-01 至 2014-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8442324
• 关键词: ATP phosphohydrolase; ATP sensitive potassium channel complex; Adenine Nucleotides; Affect; Affinity; Biochemistry; Cell membrane; Cells; Cellular biology; Chemicals; Consumption; Cytoplasm; Dendrites; Detection; Diabetes Mellitus; Diet; Diffusion; Disease; Dose; Electrophysiology (science); Energy Metabolism; Enzymes; Epilepsy; Erythrocytes; Event; Feedback; Fellowship; Fluorescence; Fluorescence Microscopy; Generations; Glucose; Glycolysis; Goals; Health; Hepatocyte; Image; Injury; Investigation; Ketone Bodies; Location; Luciferases; Mammalian Cell; Membrane; Metabolic; Metabolism; Methods; Molecular; Muscle Cells; Na(+)-K(+)-Exchanging ATPase; Names; Neurites; Neurons; Optics; Oxidative Phosphorylation; Pancreas; Photons; Probability; Process; Proteins; Pump; Regulation; Reporting; Resolution; Role; Signal Transduction; Source; Synapses; Synaptic plasticity; Vertebral column; cell type; design; imaging modality; improved; in vivo; kidney cell; luciferin; neuronal cell body; neuronal excitability; ratiometric; research study; response; sensor; small molecule; tool

DESCRIPTION (provided by applicant): Our long-term goal is to understand the relationship between metabolism and neuronal excitability and to investigate how this relationship can be altered in diseased states such as in epilepsy. Our immediate goal is to understand how compartmentation of the key metabolite ATP can modulate neuronal excitability. Energy metabolism and ATP-dependent processes are vital to all mammalian cells. A long-standing and still unresolved hypothesis is that ATP compartments exist within the cytoplasm. Evidence suggests that ATP compartmentation could be critical to the regulation of chemical and electrical signaling in many cell types, but this hypothesis is controversial. Resolution of this controversy would provide a significant advance in our basic understanding of intracellular signaling, and it has implications for our understanding of health problems such as diabetes, ischemic injuries, and epilepsy. In neurons specifically, compartmentation of ATP could be a critical factor affecting plasticity and membrane excitability. ATP compartmentation may occur because of the specialized geometry of neurons whose neurites extend far from the cell body. For example, high metabolic requirements and local ATP consumption in dendritic compartments may affect synaptic plasticity. In another scenario, restricted diffusion of ATP between the bulk cytoplasm and near the plasma membrane (the "submembrane" compartment) may impact excitability. The Na,K-ATPase is a major energy consumer in neurons, and pump activation following neuronal activity may deplete submembrane ATP. Neuronal ATP-sensitive potassium channels (KATP channels) are sensitive to submembrane ATP and ADP and could control excitability through a negative feedback loop. Although experiments using electrophysiology, biochemistry, and cell biology support an important role for ATP compartmentation, there is a lack of direct evidence. To directly investigate ATP compartmentation, better optical tools are needed for imaging intracellular ATP. Therefore, during this fellowship I will investigate ATP compartmentation in neurons with three specific aims: (1) I will develop methods for imaging the ATP-to-ADP ratio in neurons using an improved genetically-encoded, ratiometric fluorescent sensor that is targeted to subcellular locations. (2) I will investigate how ATP levels respond to neuronal activation and whether ATP is compartmented locally within dendrites or between the bulk cytoplasm and a submembrane space. (3) I will investigate how ATP levels respond to a change in fuel source and whether choice of fuel affects ATP compartmentation between the cell body, submembrane compartment, and dendrites. Using fluorescence microscopy to investigate these specific aims, I will be able to study how ATP compartmentation acts as a critical parameter in modulating neuronal excitability.

描述（由申请人提供）：我们的长期目标是了解新陈代谢和神经元兴奋性之间的关系，并研究如何在癫痫等疾病状态下改变这种关系。我们的近期目标是了解关键代谢物 ATP 的区隔如何调节神经元兴奋性。 能量代谢和 ATP 依赖性过程对所有哺乳动物细胞都至关重要。一个长期存在且尚未解决的假设是 ATP 区室存在于细胞质内。有证据表明，ATP 区室划分对于许多细胞类型的化学和电信号传导的调节至关重要，但这一假设存在争议。这一争议的解决将为我们对细胞内信号传导的基本理解提供重大进展，并且对我们对糖尿病、缺血性损伤和癫痫等健康问题的理解具有重要意义。 特别是在神经元中，ATP 的区室化可能是影响可塑性和膜兴奋性的关键因素。 ATP 区室化的发生可能是因为神经元的特殊几何形状，其神经突延伸到远离细胞体的地方。例如，树突室中的高代谢需求和局部 ATP 消耗可能会影响突触可塑性。在另一种情况下，ATP 在大量细胞质和质膜附近（“膜下”区室）之间的有限扩散可能会影响兴奋性。 Na,K-ATP 酶是神经元中的主要能量消耗者，神经元活动后的泵激活可能会耗尽膜下 ATP。神经元 ATP 敏感钾通道（KATP 通道）对膜下 ATP 和 ADP 敏感，可以通过负反馈回路控制兴奋性。尽管使用电生理学、生物化学和细胞生物学的实验支持 ATP 区室的重要作用，但缺乏直接证据。为了直接研究 ATP 区室，需要更好的光学工具来对细胞内 ATP 进行成像。因此，在本次研究金期间，我将研究神经元中的 ATP 区室，具有三个具体目标：(1) 我将开发一种方法，使用针对亚细胞的改进的基因编码、比率荧光传感器对神经元中的 ATP 与 ADP 比率进行成像。地点。 (2) 我将研究 ATP 水平如何响应神经元激活，以及 ATP 是否在树突内局部划分或在大量细胞质和膜下空间之间划分。 (3) 我将研究 ATP 水平如何响应燃料来源的变化，以及燃料的选择是否影响细胞体、膜下室和树突之间的 ATP 区室。使用荧光显微镜来研究这些特定目标，我将能够研究 ATP 区室如何作为调节神经元兴奋性的关键参数。