Exploring the ties between neuronal migration and functional development

探索神经元迁移和功能发育之间的联系

• 批准号: 8701893
• 负责人: Kimberly McArthur
• 金额: $ 5.65万
• 依托单位: CORNELL UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-04-01 至 2016-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8701893
• 关键词: Affect; Animals; Appearance; Ataxia; Automobile Driving; Behavior; Brain; Brain region; Calcium; Cells; Cephalic; Cognition; Complex; Data; Destinations; Development; Electrophysiology (science); Embryo; Epilepsy; Face; Fishes; Foundations; Gene Mutation; Genetic; Health; Image; Immigration; Knowledge; Laboratory Study; Larva; Light; Link; Location; Methods; Modeling; Morphology; Motor Neurons; Muscle; Mutation; Nerve; Nervous system structure; Neuraxis; Neuronal Migration Disorder; Neurons; Neurosciences; Pattern; Phylogeny; Physiological; Physiology; Pilot Projects; Population; Process; Property; Resources; Respiration; Role; Schizophrenia; Seizures; Structure; Swimming; Synapses; System; Techniques; Time; Travel; Universities; Vertebrates; Zebrafish; arm; extracellular; feeding; forging; hindbrain; innovation; jaw movement; migration; mutant; nervous system development; nervous system disorder; neurodevelopment; neuroepithelium; neuron development; patch clamp; presynaptic; public health relevance; respiratory; respiratory reflex; response; tool; trait

DESCRIPTION (provided by applicant): In the proposed study, I will establish fundamental principles relating structure, function, and migration in developing neurons and circuits. Neuronal migration occurs throughout the central nervous system during development, and abnormal migration contributes to a wide variety of neurological disorders, including ataxia, seizures, schizophrenia, and epilepsy. By applying a unique combination of state-of-the-art techniques and available resources in the larval zebrafish model, I hope to shed light on the complex roles of migration in circuit formation, by studying the effect of normal and abnormal migration on the development of facial branchiomotor neurons (FBMNs) in the hindbrain. These neurons undergo an early, dramatic caudal migration that is likely to serve an important functional role, bringing FBMNs closer to respiratory reflex circuits in the caudal hindbrain. Othe laboratories studying the mechanisms of migration have generated a wide variety of zebrafish mutants that specifically disrupt caudal FBMN migration without adversely affecting the general health of the animal. These circumstances present a unique opportunity to gain a foothold in the complex relationship between migration and functional development, with important consequences for our understanding of neuronal migration disorders. In Aim 1, I will define the normal endpoint of functional development by studying the functional and morphological properties of postmigratory FBMNs in larval zebrafish. I will use patch recording to quantify intrinsic physiological and rhythmic response properties of FBMNs, which likely support the role of these cells in respiratory behavior. I will also visualize the location and extent of their denditic arbors, reflecting the brain region where these neurons receive synaptic inputs. Pilot data indicates that this approach will be fruitful in describing important postmigratory FBMN traits to provide the foundation for explorations of when these properties develop with respect to migration and how they change when migration is disrupted. In Aim 2, I will explore the development of FBMN structural and functional properties during migration in zebrafish embryos to relate the progress of functional development with the migratory process. I will combine traditional intracellular recordings with calcium imaging (using a recently piloted transgenically expressed indicator) to trace the appearance of important structural and functional landmarks found in Aim 1 in order to determine which traits fail to develop until caudal migration is complete. In Aim 3, I will determine how the structural and functional properties of FBMNs are affected by disruptions to caudal migration in mutant zebrafish larvae. Using the methods of Aim 1 and armed with the knowledge gained in Aim 2, I will look for patterns in structural and functional differences between FBMNs with normal and abnormal caudal migration, to reveal the capacity (or lack thereof) of the nervous system to compensate for abnormal migration.

描述（由申请人提供）：在拟议的研究中，我将建立与发育中的神经元和回路的结构、功能和迁移相关的基本原理。神经元迁移发生在整个中枢神经系统的发展过程中，异常迁移有助于各种各样的神经系统疾病，包括共济失调，癫痫发作，精神分裂症和癫痫。通过在斑马鱼幼体模型中应用最先进的技术和可用资源的独特组合，我希望通过研究正常和异常迁移对面鳃神经元（FBMNs）发育的影响，阐明迁移在回路形成中的复杂作用。这些神经元经历了早期的，戏剧性的尾部迁移，这可能是一个重要的功能作用，使FBMNs更接近呼吸反射电路在尾部后脑。其他研究迁移机制的实验室已经产生了各种各样的斑马鱼突变体，这些突变体特异性地破坏尾部FBMN迁移，而不会对动物的一般健康产生不利影响。这些情况提供了一个独特的机会，在迁移和功能发育之间的复杂关系中站稳脚跟，对我们理解神经元迁移障碍具有重要意义。在目标1中，我将通过研究斑马鱼幼鱼中移行后FBMNs的功能和形态学特性来定义功能发育的正常终点。我将使用贴片记录来量化FBMN的内在生理和节律反应特性，这可能支持这些细胞在呼吸行为中的作用。我还将可视化它们的树突状树状结构的位置和范围，反映这些神经元接收突触输入的大脑区域。试点数据表明，这种方法将是富有成效的，在描述重要的postmigratory FBMN性状提供了基础，探索这些属性的发展时，相对于迁移，以及它们如何改变时，迁移中断。在目标2中，我将探索斑马鱼胚胎迁移过程中FBMN结构和功能特性的发展，以将功能发育的进展与迁移过程联系起来。我将结合联合收割机传统的细胞内记录与钙成像（使用最近试点转基因表达的指示剂），以跟踪在目标1中发现的重要结构和功能标志的外观，以确定哪些性状未能发展，直到尾部迁移完成。在目标3中，我将确定FBMNs的结构和功能特性如何受到突变斑马鱼幼虫尾部迁移中断的影响。使用目标1的方法和武装的知识，在目标2中，我将寻找正常和异常尾部迁移的FBMN之间的结构和功能差异的模式，以揭示神经系统的能力（或缺乏），以补偿异常迁移。