Linking Synaptic and Cognitive Deficits in a Model of Neuropsychiatric Disease

将神经精神疾病模型中的突触和认知缺陷联系起来

基本信息

  • 批准号:
    8547839
  • 负责人:
  • 金额:
    $ 8.78万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2012
  • 资助国家:
    美国
  • 起止时间:
    2012-09-20 至 2014-10-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): Recent evidence suggests that abnormalities in synaptic transmission may underlie the pathogenesis of several neuropsychiatric disorders. A better understanding of normal and aberrant synaptic function may provide improved detection and treatment strategies, thereby reducing overall disease burden. Towards these ends, the use of gene targeting in mouse has provided a unique opportunity to create laboratory animals with similar mutations to human patients that have clinically defined neuropsychiatric disorders. Thorough analysis of these mutant mice, both at the behavioral and cellular level, can thus provide a wealth of information about potential mechanisms of disease formation as well as the relationship between gene dysfunction and abnormal behavior. Evidence from a variety of human genetic association studies has highlighted the functional relevance of synaptic cell adhesion molecules (SCAMs) in neuropsychiatric disorders including autism, schizophrenia and obsesive compulsive disorder. The Neuroligin (NL)/Neurexin complex, a prototypical SCAM pair, has been implicated in excitatory and inhibitory synaptic function. In an attempt to further explore NL function, a mouse was made with a point mutation (R451C) in the NL3 gene to mimic a mutation associated with autism in a human genetics study. The goal of this proposal is to study this mutant mouse from both behavioral and synaptic perspectives, with the hope of linking abnormal behaviors to specific underlying circuit and synaptic abnormalities. Causality will then be established through attempts to ameliorate behavioral phenotypes by addressing the underlying synaptic deficits. I have chosen to focus on functional cognitive deficits, particularly cognitive flexibility, in NL3R451C mutants, as these represent a core, debilitating feature of many neuropsychiatric disorders and their underlying synaptic mechanisms have thus far received little attention. Preliminary data suggest that NL3R451C mutants have severely impaired cognitive flexibility. During the mentored phase, I will employ viral injections to localie which synapses require NL3 function to maintain cognitive flexibility. In addition, I will employ optogenetic recruitment of cortical afferent populations in the acute slice to explore abnormalities of corticostriatal synaptic transmission in the dorsal striatum of NL3R451C mutant mice. For the independent phase, I wil first explore potential abnormalities in synaptic plasticity in NL3R451C mutants. After a thorough description of the alterations of both basal transmission and activity-dependent plasticity found in the striatum of mutants, I will attempt to link these synaptic deficiencies to the observed abnormalities in cognitive flexibility through the use of cel-type and regional optogenetic manipulations. I anticipate that this proposal will uncover interesting information regarding the synaptic basis of cognitive flexibility and how perturbations of synaptic transmission in NL3R451C mutants result in rigid behavioral output. Furthermore, it will provide a template for my future studies into how other synaptic molecules mediate cognitive function.
描述(由申请人提供):最近的证据表明,突触传递异常可能是几种神经精神疾病发病机制的基础。更好地了解正常和异常的突触功能可以提供改进的检测和治疗策略,从而减少整体疾病负担。为了这些目的,在小鼠中使用基因靶向提供了一个独特的机会,以创建具有与具有临床定义的神经精神疾病的人类患者相似的突变的实验室动物。因此,在行为和细胞水平上对这些突变小鼠进行彻底分析,可以提供有关疾病形成的潜在机制以及基因功能障碍和异常行为之间关系的丰富信息。来自各种人类遗传关联研究的证据突出了突触细胞粘附分子(SCAMs)在神经精神障碍(包括自闭症、精神分裂症和强迫症)中的功能相关性。神经胶质素(NL)/Neurexin复合物是一种典型的SCAM对,与兴奋性和抑制性突触功能有关。为了进一步探索NL功能,在NL 3基因中产生了点突变(R451 C)的小鼠,以模拟人类遗传学研究中与自闭症相关的突变。该提案的目标是从行为和突触的角度研究这种突变小鼠,希望将异常行为与特定的潜在电路和突触异常联系起来。然后,通过解决潜在的突触缺陷来改善行为表型,从而建立因果关系。我选择关注NL 3R 451 C突变体的功能性认知缺陷,特别是认知灵活性,因为这些代表了许多神经精神疾病的核心,使人衰弱的特征,其潜在的突触机制迄今为止很少受到关注。初步数据表明,NL 3R 451 C突变体严重损害了认知灵活性。在指导阶段,我将使用病毒注射来定位哪些突触需要NL 3功能来保持认知灵活性。此外,我将采用急性切片中皮质传入群体的光遗传学招募来探索NL 3R 451 C突变小鼠背侧纹状体中皮质纹状体突触传递的异常。对于独立阶段,我将首先探索突触可塑性的潜在异常 在NL 3R 451 C突变体中。在对突变体纹状体中发现的基础传递和活动依赖性可塑性的改变进行彻底描述之后,我将尝试通过使用细胞类型和区域光遗传学操作将这些突触缺陷与观察到的认知灵活性异常联系起来。我预计,这一提议将揭示有关认知灵活性的突触基础以及扰动如何影响认知灵活性的有趣信息。 NL 3R 451 C突变体的突触传递导致刚性行为输出。此外,它将为我未来研究其他突触分子如何介导认知功能提供模板。

项目成果

期刊论文数量(1)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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Marc V Fuccillo其他文献

Marc V Fuccillo的其他文献

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{{ truncateString('Marc V Fuccillo', 18)}}的其他基金

Novel Role of a Ventral Striatal Circuit in Motor Control
腹侧纹状体电路在运动控制中的新作用
  • 批准号:
    10469310
  • 财政年份:
    2021
  • 资助金额:
    $ 8.78万
  • 项目类别:
Novel Role of a Ventral Striatal Circuit in Motor Control
腹侧纹状体电路在运动控制中的新作用
  • 批准号:
    10676802
  • 财政年份:
    2021
  • 资助金额:
    $ 8.78万
  • 项目类别:
A Novel Role for Local Striatal Interneuron Regulation of Goal-Directed Action
局部纹状体中间神经元调节目标导向行动的新作用
  • 批准号:
    10338165
  • 财政年份:
    2020
  • 资助金额:
    $ 8.78万
  • 项目类别:
A Novel Role for Local Striatal Interneuron Regulation of Goal-Directed Action
局部纹状体中间神经元调节目标导向行动的新作用
  • 批准号:
    10558680
  • 财政年份:
    2020
  • 资助金额:
    $ 8.78万
  • 项目类别:
Molecular and Circuit Mechanisms of Neurexin1-Mediated Goal-Directed Dysfunction
Neurexin1 介导的目标导向功能障碍的分子和电路机制
  • 批准号:
    10300008
  • 财政年份:
    2017
  • 资助金额:
    $ 8.78万
  • 项目类别:
Molecular and Circuit Mechanisms of Neurexin1-Mediated Goal-Directed Dysfunction
Neurexin1 介导的目标导向功能障碍的分子和电路机制
  • 批准号:
    10058775
  • 财政年份:
    2017
  • 资助金额:
    $ 8.78万
  • 项目类别:
Linking Synaptic and Cognitive Deficits in a Model of Neuropsychiatric Disease
将神经精神疾病模型中的突触和认知缺陷联系起来
  • 批准号:
    9069064
  • 财政年份:
    2012
  • 资助金额:
    $ 8.78万
  • 项目类别:
Linking Synaptic and Cognitive Deficits in a Model of Neuropsychiatric Disease
将神经精神疾病模型中的突触和认知缺陷联系起来
  • 批准号:
    8424086
  • 财政年份:
    2012
  • 资助金额:
    $ 8.78万
  • 项目类别:
Synaptic Analysis of Neuroligin1 function
Neuroligin1 功能的突触分析
  • 批准号:
    7676907
  • 财政年份:
    2009
  • 资助金额:
    $ 8.78万
  • 项目类别:
Synaptic Analysis of Neuroligin1 function
Neuroligin1 功能的突触分析
  • 批准号:
    7895499
  • 财政年份:
    2009
  • 资助金额:
    $ 8.78万
  • 项目类别:

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