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Clonal Analysis of Neocortical Interneuron Circuit Development

新皮质中间神经元回路发育的克隆分析

基本信息

批准号：
8028025
负责人：
Song-Hai Shi
金额：
$ 28.64万
依托单位：
SLOAN-KETTERING INST CAN RESEARCH
依托单位国家：
美国
项目类别：
财政年份：
2010
资助国家：
美国
起止时间：
2010-09-01 至 2012-08-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8028025
关键词：
Address Arts Autistic Disorder Biological Neural Networks Brain Brain Diseases Cells Cognition Complex Development Electrodes Electrophysiology (science)Engineering Epilepsy Etiology Functional disorder Genetic Glutamates Goals Image Individual Infection Interneurons Knowledge Label Laser Scanning Microscopy Light Link Medical Mental disorders Methods Mission Modeling Mus Neocortex Neurologic Neurons Output Physiological Process Production Property Radial Research Retroviridae Rodent Schizophrenia Sister Stem cells Structure Surface Synapses Techniques Telencephalon Testing Therapeutic Intervention Visual Cortex base density excitatory neuron gamma-Aminobutyric Acid in utero information processing inhibitory neuron innovation insight language perception malformation migration neocortical nerve stem cell neuronal cell body orientation selectivity patch clamp psychologic public health relevance tool two-photon white matter

项目摘要

DESCRIPTION (provided by applicant): Virtually all neuronal circuits in the mammalian neocortex are composed of glutamatergic excitatory neurons and GABAergic inhibitory interneurons. While excitatory neurons are responsible for generating the output, interneurons provide a rich variety of inhibitions through an extraordinary diversity in subtypes that often determine output. Extensive studies over the past decade have revealed key insights into the production and organization of excitatory neurons in the neocortex. In contrast, our knowledge of interneuron production and organization in the neocortex remains very limited. For example, it is unclear whether a single interneuron progenitor cell gives rise to different subtypes of interneurons and whether sister interneurons originating from the same progenitor cell are specifically organized and thereby provide potential anatomical substrates for the formation of functional circuits in the neocortex. To address these fundamental questions, we propose to perform clonal analysis of interneuron production, migration and structural and functional organization in the neocortex. To achieve our goals, we will develop innovative methods for effectively and selectively labeling interneuron progenitor cells in the ventral telencephalon - the ganglionic eminences - at clonal density. We will analyze the production, migration, and structural and functional organization of individual interneuron clones being labeled using state-of-the-art imaging (e.g. two photon lasers scanning microscopy) and electrophysiology (e.g. multi-electrode whole-cell patch clamp recording) approaches and link these processes to functional circuit formation in the neocortex. Interneuron malformation and dysfunction have been associated with many neurological and psychological disorders, such as epilepsy, schizophrenia and autism. Therefore, our research will not only provide fundamental insights into interneuron development and greatly advance our understanding of the functional organization of the neocortex, but will also shed light on the etiology of many devastating brain disorders. 1 PUBLIC HEALTH RELEVANCE: Interneurons are vital components of neural networks in the brain and are responsible for providing a rich variety of inhibition actions that restrain the brain activity. Malformation and dysfunction of interneruons have been linked to many neurological and psychological illnesses, including epilepsy, schizophrenia and autism. Our studies on interneuron production and organization in the mammalian brain will shed light on the etiology and thereby provide new ideas for the medical treatment of many of these devastating brain disorders. 1

描述(申请人提供)：哺乳动物大脑皮层中几乎所有的神经元回路都由谷氨酸能兴奋性神经元和GABA能抑制中间神经元组成。虽然兴奋性神经元负责产生输出，但中间神经元通过决定输出的亚型的异常多样性提供了丰富的抑制。在过去的十年中，广泛的研究揭示了对新皮质兴奋性神经元的产生和组织的关键见解。相比之下，我们对新皮质中神经元间的产生和组织的了解仍然非常有限。例如，尚不清楚单个中间神经元前体细胞是否产生不同亚型的中间神经元，以及起源于同一前体细胞的姐妹中间神经元是否具有特定的组织结构，从而为新皮质功能回路的形成提供潜在的解剖学基础。为了解决这些基本问题，我们建议对新皮质中的中间神经元的产生、迁移以及结构和功能组织进行克隆分析。为了实现我们的目标，我们将开发创新的方法，以克隆密度有效和选择性地标记腹侧端脑-神经节隆起-的神经元间祖细胞。我们将使用最先进的成像(例如双光子激光扫描显微镜)和电生理学(例如多电极全细胞膜片钳记录)方法分析被标记的单个中间神经元克隆的产生、迁移以及结构和功能组织，并将这些过程与新皮质中的功能电路形成联系起来。神经元间的畸形和功能障碍与许多神经和心理疾病有关，如癫痫、精神分裂症和自闭症。因此，我们的研究不仅将为神经元间发育提供基本的见解，极大地促进我们对新皮质功能组织的理解，而且还将有助于揭示许多破坏性大脑疾病的病因。1 与公共健康相关：中间神经元是大脑神经网络的重要组成部分，负责提供丰富多样的抑制作用，抑制大脑活动。互联网的畸形和功能障碍与许多神经和心理疾病有关，包括癫痫、精神分裂症和自闭症。我们对哺乳动物大脑中中间神经元的产生和组织的研究将有助于揭示其病因，从而为许多这些破坏性的大脑疾病的医学治疗提供新的思路。1