Cellular and Molecular Mechanisms of Early Cortical Development

早期皮质发育的细胞和分子机制

• 批准号: 7700139
• 负责人: ERIC Christopher OLSON
• 金额: $ 24.04万
• 依托单位: UPSTATE MEDICAL UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-09-30 至 2014-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7700139
• 关键词: Actins; Acute; Adaptor Signaling Protein; Adult; Architecture; Autistic Disorder; Behavior; Behavior Control; Brain; Cell-Cell Adhesion; Cells; Cerebral cortex; Cerebrum; Cognition; Cortical Malformation; Data; Defect; Development; Dyslexia; Embryo; Epilepsy; Etiology; Event; Exposure to; F-Actin; Focal Adhesions; Healed; Hereditary Disease; Image; Indium; Infection; Ligands; Mediating; Medical; Mental Retardation; Modeling; Molecular; Morphology; Movement; Mus; Neuraxis; Neurites; Neuronal Differentiation; Neurons; Phenotype; Photons; Positioning Attribute; Post-Translational Protein Processing; Proteins; RNA Interference; Radiation; Reading Disorder; Recombinants; Recovery of Function; Reeler Mouse; Reelin Signaling Pathway; Regulation; Reporter; Research Personnel; Role; Signal Transduction; Signaling Protein; Staging; Structure; Testing; Time; Toxin; Universities; Work; base; brain malformation; cell motility; healing; inhibitor/antagonist; insight; migration; nerve injury; novel; overexpression; paxillin; polymerization; protein expression; public health relevance; response

DESCRIPTION (provided by applicant): The developing cerebral cortex is a sensitive target for genetic diseases and for gestational exposure to toxins, infection and radiation. Despite this, the basic cellular and molecular mechanisms of cortical development, particularly early cortical development are not well understood. Using a novel 3D cortical hemisphere explant approach and reporter mice, we will examine the cellular behaviors that initiate cortical plate formation and determine how the secreted ligand, Reelin coordinates these behaviors. We will focus on the role of Reelin-dependent modulation of the focal adhesion adaptor protein Paxillin that we find dynamically expressed during early cortical development and aberrantly expressed in reeler mice cortices that lack Reelin. We are using pharmacological and RNAi-based approaches to target downstream signaling elements in the Reelin signaling pathway to determine Reelin's and Paxillin's role(s) in triggering and/or sustaining this morphological differentiation and motility. These studies will help resolve competing models of Reelin function, while providing further molecular and cellular insights into the formation of a cellular layer of the cerebral cortex. Insight into Reelin's role in cortical development will provide a general insight into the development and organization of neurons throughout the central nervous system. In adults, Reelin is up regulated in epileptic foci, and in response to nerve injury. Reelin may therefore have additional important roles in healing and functional recovery. PUBLIC HEALTH RELEVANCE: Brain malformations are increasingly appreciated as an underlying cause of certain forms of epilepsy, mental retardation, autism, dyslexia and reading disorders. This proposal examines molecular and cellular events that occur at an early stage of brain development, but that have a major impact on later brain function and cognition. The work will provide a framework for understanding the etiology of cerebral cortical malformations.

描述(申请人提供)：发育中的大脑皮层是遗传病和妊娠暴露于毒素、感染和辐射的敏感目标。尽管如此，皮质发育，特别是早期皮质发育的基本细胞和分子机制还没有被很好地理解。使用一种新的3D皮质半球外植体方法和报告小鼠，我们将检查启动皮质板形成的细胞行为，并确定分泌配体Reelin如何协调这些行为。我们将专注于Reelin依赖的对粘着斑适配器蛋白paxlin的调节作用，我们发现这种蛋白在皮质发育的早期动态表达，并在缺乏Reelin的卷轴小鼠皮质中异常表达。我们正在使用药理学和基于RNA干扰的方法来靶向Reelin信号通路中的下游信号元件，以确定Reelin和帕西林在触发和/或维持这种形态分化和运动中的作用(S)。这些研究将有助于解决Reelin功能的相互竞争的模型，同时为大脑皮层细胞层的形成提供进一步的分子和细胞洞察。深入了解Reelin在皮质发育中的作用将提供对整个中枢神经系统神经元的发育和组织的总体洞察。在成人中，Reelin在癫痫灶和对神经损伤的反应中上调。因此，Reelin可能在愈合和功能恢复方面具有额外的重要作用。 与公共卫生相关：大脑畸形越来越被认为是某些形式的癫痫、智力低下、自闭症、阅读障碍和阅读障碍的根本原因。这项建议研究了发生在大脑发育早期的分子和细胞事件，但这些事件对后来的大脑功能和认知有重大影响。这项工作将为理解大脑皮层畸形的病因提供一个框架。