Proj 1: Influeence of proteoglycans on Gliogeness and Embryonic Brain Injury

项目 1：蛋白多糖对神经胶质形成和胚胎脑损伤的影响

• 批准号: 8814115
• 负责人: NANCY B SCHWARTZ
• 金额: $ 24.46万
• 依托单位: UNIVERSITY OF CHICAGO
• 依托单位国家: 美国
• 资助国家: 美国
• 起止时间: 至 2017-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8814115
• 关键词: Acute; Address; Adult; Affect; Apoptosis; Area; Astrocytes; Attention; Axon; Behavioral; Biological; Brain; Brain Injuries; Cell Differentiation process; Cells; Cerebral Palsy; Chondroitin Sulfate Proteoglycan; Cognitive; Cognitive deficits; Communication; Complex; Development; Disease; Embryo; Environment; Epilepsy; Experimental Models; Fostering; Future; Genes; Genetic; Glial Differentiation; Goals; Healed; Inflammation; Injury; Instruction; Knowledge; Lead; Lesion; Mental Retardation; Metabolism; Modeling; Morbidity - disease rate; Natural regeneration; Neonatal; Nervous system structure; Neuraxis; Neurodevelopmental Disability; Neuroglia; Neurological outcome; Neurons; Oligodendroglia; Periventricular white matter injury; Phenotype; Predisposition; Prenatal Injuries; Preparation; Process; Production; Proteoglycan; Research; Role; Scheme; Signal Pathway; Signal Transduction; Slice; Stab Wounds; Supporting Cell; System; Therapeutic; Time; Transcriptional Regulation; Trauma; Tretinoin; Ventricular; Work; adverse outcome; aggrecan; axon regeneration; base; cell motility; central nervous system injury; critical period; extracellular; fetal; gliogenesis; healing; hindbrain; in vivo; innovation; insight; migration; mortality; neonatal human; nerve stem cell; nervous system development; neural patterning; neuropathology; novel; oligodendrocyte precursor; programs; research study; response; response to injury; stem cell population; tool

PROJECT SUMMARY (See instructions): Prerinatal injury is a significant cause of morbidity and mortality, often with long term cognative sequelae. Increasingly, different forms of injury inflicted during highly susceptible periods of development produce similar phenotypes involving behavioral and cognitive deficits and mental retardation. Importantly, the susceptibility period for the most common forms of developmental brain injuries coincides with oligodendrocyte and astrocyte differentiation and maturation. Project 1 focuses on the role of the extracellular milieu in promoting specification and migration of cells of the glial lineage during normal central nervous system (CNS) development and after traumatic embryonic brain injury. Future studies are informed by several recent findings: the demonstration of a role for aggrecan in gliogenesis; establishment of a hindbrain organotypic culture system which faithfully recapitulates the native in vivo cytoarchitecture and cell environment; and development of an acute embryonic injury model enabling the study of the protective or inhibitory role of the matrix following embryonic injury. Two aims are proposed: Aim 1, To analyze glial cell migration and differentiation and the importance of the extracellular milieu; Aim 2, To elucidate the response of glial precursors to embryonic brain injury and the function of proteoglycans in this process. These studies will provide insights into mechanisms controlling astrogliogenesis and the influence of components of the glial cell precursors' environment on cell-fates, as well as elucidate how glial precursor differentiation is affected by cell-environment changes induced by trauma during brain development. Understanding the mechanisms which underlie these relationships is critical to being able to remodel the composition of the extracellular milieu, thereby influencing cell-fate during development, and devising novel therapies to foster regeneration after CNS injury.

项目概述（见说明）：