ASTROCYTE-NEURONAL INTERACTIONS IN THE VISUAL CORTEX
ASTROCYTE-NEURONAL INTERACTIONS IN THE VISUAL CORTEX
批准号:
8022707
负责人:
Ken Douglas McCarthy
金额:
$45.9万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-01-01 至 2015-12-31
关键词:
AnimalsAreaAstrocytesBehaviorBehavioralBiological ModelsBlood VesselsBlood flowBrainCalciumCalcium SignalingCellsChelating AgentsClinicalCoupledDevelopmentDiseaseExhibitsG-Protein-Coupled ReceptorsGenetically Engineered MouseHippocampus (Brain)HyperemiaImageIn SituIn VitroKnock-outLaboratoriesLateral Geniculate BodyLeadLifeLightLinkMaintenanceMeasurableMicrogliaModelingMusNeuronsNeurotransmitter ReceptorOcular DominanceOligodendrogliaPathway interactionsPhysiologyPlayProcessRelative (related person)ReportingResearch PersonnelRoleSensorySignal TransductionSliceSpinal CordSynapsesSynaptic TransmissionSynaptic plasticitySystemTestingVisionVision DisordersVisualVisual CortexVisual PathwaysVisual system structurearea striatacaged moleculecell typeexperiencefunctional outcomeshuman CCR10 proteinin vivonovel therapeuticsrelating to nervous systemrelease of sequestered calcium ion into cytoplasmresponsesensory stimulus
中文摘要
描述(由申请人提供):星形胶质细胞是脑中占主导地位的细胞类型,与所有其他神经细胞类型密切相关,表现出广泛的神经递质受体,对神经元活动作出反应,并释放神经活性分子;尽管如此,我们对这些细胞在生理学、行为或疾病中的作用知之甚少。这一领域的一个主要限制是缺乏模型,允许在活体动物的感觉刺激后的神经系统中的星形胶质细胞功能的研究。到目前为止,几乎所有的研究星形胶质细胞的功能都依赖于药理学方法来激活或抑制这些细胞中的信号传导,并记录其活性对周围细胞在体外或原位的影响。我们认为,这一领域的进展需要一个模型系统,其中:1)活体动物的感觉输入可用于激活星形胶质细胞信号传导,2)行为读数可用于确定体内星形胶质细胞信号传导的功能结果。为此,我们建议使用小鼠中央视觉通路,研究星形胶质细胞信号级联在突触传递和可塑性以及视觉中的作用。在《特定目标1》中,我们将使用特性良好的初级视皮层切片来研究原位调节星形胶质细胞信号传导的途径和机制。在特定目标2中,我们将使用体内成像来确定星形胶质细胞的钙反应是否是空间限制性的,并且在局部控制血管张力中是否重要。在第三章中,我们将使用活体成像和转基因小鼠来研究星形胶质细胞在视觉可塑性中的作用。最后,在《特定目标4》中,我们将通过基因工程改造小鼠来研究星形胶质细胞在视觉中的作用,这是一种将感觉输入到视觉皮层的行为读出器。总的来说,这些研究的结果应该澄清的条件下,感觉输入导致星形胶质细胞信号的激活和星形胶质细胞信号在突触传递和视觉的作用。
公共卫生相关性:星形胶质细胞是大脑中占主导地位的细胞类型,与所有其他神经细胞类型密切相关,表现出广泛的神经递质受体,对神经元活动做出反应,并释放神经活性分子;尽管如此,我们对这些细胞在生理学,行为或疾病中的作用知之甚少。了解星形胶质细胞在视觉皮层中的作用可能会导致视觉障碍的新治疗方法。
英文摘要
DESCRIPTION (provided by applicant): Astrocytes are the predominate cell type in brain, closely associate with all other neural cell types, exhibit a wide array of neurotransmitter receptors, respond to neuronal activity, and release neuroactive molecules; in spite of this, we know very little about the role of these cells in physiology, behavior, or disease. A major limitation in this area is the lack of models that permit the study of astrocyte function in neural systems following sensory stimulation in living animals. To date, nearly all studies of astrocytic function have relied on pharmacological approaches to activate or inactivate signaling in these cells and to record the effects of their activity on surrounding cells in vitro or in situ. It is our view that progress in this area requires a model system where: 1) sensory input in living animals can be used to activate astrocytic signaling and, 2) behavioral readouts are available for determining the functional outcome of astrocytic signaling in vivo. To this end, we propose to use the mouse central visual pathway to investigate the role of astrocytic signaling cascades in synaptic transmission and plasticity as well as in vision. In Specific Aim 1 we will use well-characterized slices of primary visual cortex to examine the pathways and mechanisms regulating astrocytic signaling in situ. In Specific Aim 2 we will use in vivo imaging to determine if astrocytic calcium responses are spatially-restricted and important in the local control of vascular tone. In Specific Aim 3 we will use in vivo imaging and genetically- modified mice to investigate the role of astrocytes in visual plasticity. Finally, in Specific Aim 4 we will genetically engineered mice to investigate the role of astrocytes in vision, a behavioral readout of sensory input into the visual cortex. Overall, the results of these studies should clarify the conditions where sensory input leads to the activation of astrocytic signaling and the role of astrocytic signaling in synaptic transmission and vision.
PUBLIC HEALTH RELEVANCE: Astrocytes are the predominate cell type in brain, closely associate with all other neural cell types, exhibit a wide array of neurotransmitter receptors, respond to neuronal activity, and release neuroactive molecules; in spite of this, we know very little about the role of these cells in physiology, behavior, or disease. Understanding the role that astrocytes play in the visual cortex could lead to new therapeutic treatments of visual disorders.
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会议论文
Function of Astrocytic GPCR Signaling Cascades in Physiology and Mental Illness
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批准号:8442109
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项目类别:
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资助金额:$34.2万
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财政年份:2013
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负责人:Ken Douglas McCarthy
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依托单位:
Function of Astrocytic GPCR Signaling Cascades in Physiology and Mental Illness
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批准号:8629792
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财政年份:2013
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Function of Astrocytic GPCR Signaling Cascades in Physiology and Mental Illness
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批准号:9020268
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资助金额:$34.2万
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Glial Modulation of Autonomic Nervous System Activity
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批准号:8429591
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财政年份:2012
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Glial Modulation of Autonomic Nervous System Activity
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批准号:8535858
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财政年份:2012
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负责人:Ken Douglas McCarthy
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依托单位:
SPINAL CORD ASTROCYTES AND CHRONIC PAIN
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批准号:8361931
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项目类别:
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财政年份:2011
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INVESTIGATING EARLY ULTRASTRUCTURAL CHANGES IN THE PATHOGENESIS OF HYDROCEPHALUS
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批准号:8361941
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项目类别:
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依托单位:
ASTROCYTE-NEURONAL INTERACTIONS IN THE VISUAL CORTEX
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批准号:8787739
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项目类别:
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资助金额:$39.57万
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财政年份:2011
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ASTROCYTE-NEURONAL INTERACTIONS IN THE VISUAL CORTEX
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批准号:8597430
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项目类别:
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资助金额:$39.81万
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财政年份:2011
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负责人:Ken Douglas McCarthy
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ASTROCYTE-NEURONAL INTERACTIONS IN THE VISUAL CORTEX
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批准号:8403633
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项目类别:
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资助金额:$42.87万
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财政年份:2011
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负责人:Ken Douglas McCarthy
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依托单位:
ASTROCYTE-NEURONAL INTERACTIONS IN THE VISUAL CORTEX
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批准号:8206491
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项目类别:
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资助金额:$45.13万
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财政年份:2011
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负责人:Ken Douglas McCarthy
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依托单位:
SPINAL CORD ASTROCYTES AND CHRONIC PAIN
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批准号:8169647
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项目类别:
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资助金额:$2.39万
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依托单位:
Role of Spinal Cord Lamina II Astrocytes in Neurophysiology and Chronic Pain
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批准号:7385710
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项目类别:
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资助金额:$28.56万
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财政年份:2008
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负责人:Ken Douglas McCarthy
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依托单位:
Role of Spinal Cord Lamina II Astrocytes in Neurophysiology and Chronic Pain
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批准号:7765500
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项目类别:
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资助金额:$31.48万
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财政年份:2008
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负责人:Ken Douglas McCarthy
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依托单位:
Analysis of Genomic and Proteomic Changes in Glia That Lead To Hydrocephalus
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批准号:7587317
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项目类别:
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资助金额:$18.15万
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财政年份:2008
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负责人:Ken Douglas McCarthy
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依托单位:
Role of Spinal Cord Lamina II Astrocytes in Neurophysiology and Chronic Pain
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批准号:7535561
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项目类别:
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资助金额:$31.79万
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财政年份:2008
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负责人:Ken Douglas McCarthy
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依托单位:
Analysis of Genomic and Proteomic Changes in Glia That Lead To Hydrocephalus
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批准号:7451185
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项目类别:
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资助金额:$21.81万
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财政年份:2008
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依托单位:
ASTROCYTIC REGULATION OF NEURONAL EXCITABILITY IN VIVO
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批准号:2272992
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项目类别:
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资助金额:$20.77万
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财政年份:1996
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负责人:Ken Douglas McCarthy
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依托单位:
ASTROCYTIC REGULATION OF NEURONAL EXCITABILITY IN VIVO
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批准号:2771944
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项目类别:
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资助金额:$22.23万
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财政年份:1996
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负责人:Ken Douglas McCarthy
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依托单位:
ASTROCYTIC REGULATION OF NEURONAL EXCITABILITY IN VIVO
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批准号:6393705
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项目类别:
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资助金额:$37.81万
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财政年份:1996
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