课题基金 / 基金详情

GENETIC, PHYSIOLOGICAL, AND BEHAVIORAL STUDIES OF MEMORY

GENETIC, PHYSIOLOGICAL, AND BEHAVIORAL STUDIES OF MEMORY
记忆的遗传、生理和行为研究
批准号:
6392408
负责人:
SUSUMU TONEGAWA
金额:
$127.92万
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-09-30 至 2004-08-31

项目摘要

项目成果

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中文摘要
翻译
描述:(改编自申请人的摘要)这是一份建立Silvio O的申请。Conte Center for Neuroscience Research(CCNR)on Genetic,Physiological,AND Behavioral Studies OF Memory.该中心的长期目标是阐明哺乳动物学习和记忆的分子,细胞和神经元的整体机制。CCNR在三个层面上解决了这个问题。首先,它试图了解海马和新皮层中突触可塑性的基本机制,以及这些是如何发育和区域调节的。其次,该中心试图了解海马体和新皮层中的神经元活动如何代表有关外部世界的信息,这些信息如何与以前的经验进行比较,以及这些表征如何巩固到长期记忆中。第三,该中心试图将突触可塑性和学习的神经元相关性与记忆的行为措施联系起来。突触可塑性的基本机制将通过应用电生理学技术,从海马和视觉和颞下皮质的小鼠与几个特定的空间靶向遗传病变(基因敲除小鼠)的脑切片进行研究。一种新的电生理技术,允许单个可视化的突触的培养神经元的分析也将用于这些小鼠的分析。为了了解神经元活动如何代表学习信息,该中心将寻求通过将新颖的多个四极记录技术应用于正在进行各种记忆任务的猴子或啮齿动物来识别海马体、下颞叶皮层和前额叶皮层中神经元集合活动的变化。最后,为了将突触可塑性和学习的神经元相关性与记忆的行为措施联系起来,该中心利用了在小鼠中进行区域和时间选择性遗传破坏的新方法,其中一些方法已经在该中心开发(海马CAI选择性),而另一些方法(新皮层和新皮层亚区域特异性)被提议作为核心项目开发。拟议的研究是真正的跨学科研究,涵盖小鼠的分子遗传学,大鼠和小鼠脑切片和培养神经元的电生理学,以及猴子,大鼠和基因工程小鼠执行特定记忆任务的多个电极记录。来自三个机构的六名研究人员和作为分包商的第七名研究人员,每个人都拥有互补的和公认的专业知识和最先进的实验技术,将在CCNR框架内联合起来并广泛合作。该中心的研究与心理健康和疾病高度相关,因为记忆障碍是衰老和精神分裂症、阿尔茨海默病和帕金森病等主要神经系统疾病的标志。
英文摘要
DESCRIPTION: (Adapted from the applicant's abstract) This is an application to establish a Silvio O. Conte Center for Neuroscience Research (CCNR) on GENETIC, PHYSIOLOGICAL, AND BEHAVIORAL STUDIES OF MEMORY. The long-term objective of the Center is to elucidate the molecular, cellular, and neuronal ensemble mechanisms of mammalian learning and memory. The CCNR attacks the problem at three levels. First, it seeks to understand the elementary mechanisms of synaptic plasticity in the hippocampus and neocortex, and how these are developmentally and regionally regulated. Second, the Center seeks to understand how neuronal activity in the hippocampus and neocortex represents information about the outside world, how this information is compared with previous experience, and how these representations are consolidated into long-term memory. Third, the Center seeks to connect the synaptic plasticity and the neuronal correlates of learning with behavioral measures of memory. The elementary mechanisms of synaptic plasticity will be studied by applying electrophysiological techniques to brain slices derived from the hippocampus and the visual and inferotemporal cortices of mice with several specific spatially targeted genetic lesions (knockout mice). A novel electrophysiological technique that permits the analysis of single visualized synapses of cultured neurons will also be used for the analysis of these mice. In order to understand how neuronal activity represents learned information, the Center will seek to identify alterations in the activity of neuronal ensembles in the hippocampus, inferotemporal cortex, and prefrontal cortex by applying the novel multiple tetrode recording techniques to monkeys or rodents that are undertaking various memory tasks. Finally, in order to connect synaptic plasticity and neuronal correlates of learning with behavioral measures of memory, the Center takes advantage of the new methods of regionally and temporally selective genetic disruptions in mice, some of which have already been developed in the Center (hippocampus CAI-selective) while others (neocortex and neocortical subregion-specific) are proposed to be developed as a core project. The proposed research is truly interdisciplinary covering molecular genetics of mice, electrophysiology of brain slices and cultured neurons from rats and mice, and multiple electrode recordings of monkeys, rats, and genetically engineered mice performing specific memory tasks. Six investigators from three institutions and the seventh investigator as a subcontractor, each possessing complimentary and well-recognized expertise and state of the art experimental technologies will join forces and collaborate extensively in the CCNR framework. The Center's research is highly relevant to mental health and illness because mnemonic impairments are a hallmark of aging and major neurological diseases such schizophrenia, Alzheimer's disease and Parkinson's disease.
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会议论文
CORE 1: Genetically Engineered Mice for Collaborations
Project 2: Role of synaptic Plasticity in Hippocampal Memory
CORE 2: Maintaining Genetically Engineered Mice for Collaborations
CORE 3: Administration
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