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CONTROL OF CELL MIGRATION IN DEVELOPING BRAIN

CONTROL OF CELL MIGRATION IN DEVELOPING BRAIN
大脑发育中细胞迁移的控制
批准号:
3407406
负责人:
Richard S Nowakowski
金额:
$11.26万
依托单位国家:
美国
项目类别:
财政年份:
1985
资助国家:
美国
项目状态:
已结题
起止时间:
1985-09-01 至 1988-04-30

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中文摘要
翻译
本研究的目的是为了更好地了解 导致年轻神经元脱离增殖区的一系列事件 它在成熟大脑中的正确位置,开始理解它是如何 特定的基因可能有助于(和/或破坏)迁移过程, 并分析处于错误位置的神经元, 在差异化的同时调整其连接性。 的方法 将利用小鼠中存在的突变, 它破坏了发育中的中枢神经系统中神经元的迁移 系统,从而产生成人大脑的畸形, 特定的神经元群体位于异常位置。 具体 本项目的目标是:1)确定开发流程 由四种不同的遗传缺陷修饰, 最终由年轻的神经元在从大脑迁移到大脑的过程中承担。 增殖区的发展过程中,他们的最终位置 中枢神经系统,2)分析在成熟的中枢神经 神经元轴突和树突分支的变化 它们在发育期间会迁移到错误的位置。 实验将进行,这将:1)探索相对 迁移神经元本身的贡献,放射状胶质细胞, 先前产生的神经元,以及来自邻近结构的轴突, 影响幼鱼迁徙轨迹上的“停止”点沿着 神经元,2)分析具有以下特征的神经元之间的形态差异: 站在“错误”的立场上,站在“正确”的立场上, 立场,和3)澄清实验的遗传学的一些方面, situations. 这项工作意义重大,因为它对 了解细胞迁移过程中的发展,中央 神经系统
英文摘要
The goals of this research are to reach a better understanding of the sequence of events which lead a young neuron from the proliferative zones to its proper position in the mature brain, to begin to understand how specific genes might contribute to (and/or disrupt) the migratory process, and to analyze the capacity of neurons which are in the wrong position to make adjustments in their connectivity while differentiating. The approach to be taken will be to exploit the existence of mutations in the mouse which disrupt the migration of neurons in the developing central nervous system and thereby produce malformations of the adult brain in which specific populations of neurons reside in abnormal positions. Specific aims of this project are: 1) to determine the development processes modified by four different genetic defects which affect the position ultimately assumed by young neurons during their migration from the proliferative zone to their final position during the development of the central nervous system, and 2) to analyze in the mature central nervous system the changes in the axonal and dendritic arborizations of neurons which migrate to the wrong position during the developmental period. Experiments will be conducted which will: 1) explore the relative contributions of the migrating neurons themselves, of radial glial cells, of previously generated neurons, and of axons from adjacent structures in influencing the "stopping" point along the migratory trajectory of a young neuron, 2) analyze the morphological differences between neurons which have reached a "wrong" position and those which have assumed the "correct" position, and 3) clarify some aspects of the genetics of the experimental situations. This work is significant because of its contribution to the understanding of cell migration during the development of the central nervous system.
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