CRCNS: Linking Synaptic Populations and Computation Using Statistical Mechanics
CRCNS:使用统计力学将突触群体和计算联系起来
基本信息
- 批准号:10830119
- 负责人:
- 金额:$ 26.13万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2023
- 资助国家:美国
- 起止时间:2023-08-01 至 2028-04-30
- 项目状态:未结题
- 来源:
- 关键词:AddressArchitectureAreaAwarenessBeautyBehaviorBiologyBooksBrainCharacteristicsChildClinicalCodeComplexDendritic SpinesDevelopmentDiseaseEducationEducational workshopEnsureEntropyFerretsFunctional disorderGeneral PopulationImageIndividualInterdisciplinary StudyKnowledgeLeadLinkLocationMeasuresMindModelingNatureNeurobiologyNeuronsNeurosciencesOutputPatternPennsylvaniaPersonsPhysicsPopulationProbabilityProgram DevelopmentPropertyResearch PersonnelSTEM fieldScienceScientific Advances and AccomplishmentsScientistSensoryStatistical MechanicsStructureSynapsesTalentsTrainingTreesUniversitiesVisual CortexWeightWorkbiophysical modelcalcium indicatorcareercareer developmentcomputational neurosciencedeep neural networkdesignexperimental studyhigh schoolin vivolecturesnervous system disorderneuralnext generationnovelnovel strategiesoutreachpublic health relevanceskillsstatisticssynaptic functiontheoriestwo photon microscopyundergraduate student
项目摘要
Computations performed by single neurons result from integration of a large myriad of synaptic inputs
distributed throughout complex dendritic topology. Synaptic inputs vary in substantial ways; sensory-driven
activity patterns, probability of activation, synapse location within the dendritic topology, local dendritic
organization, and ultrastructural characteristics are all thought to be critical for determining how synaptic
inputs influence the spiking output of a neuron. Populations of synaptic inputs, ultimately, determine the
coding capacity and computations single neurons can perform. Despite this fact, studies largely overlook the
synaptic input population within a single neuron, instead focusing on the activity of cellular populations, using
biophysical models or constructing models that create hypothetical weights or synapses (e.g. deep-neural
networks). Thus, a critical question in neuroscience remains how ensemble synaptic activity is integrated in
vivo and what are the fundamental principles of synaptic organization which describe neural computation.
To address this issue, we present a tightly integrated experiment-theory approach. We propose to (1)
measure the sensory-driven activity patterns of large populations of dendritic spines on layer 2/3 visual
cortical neurons in ferret visual cortex in vivo, and (2) use a statistical physics approach to characterize the
structure and computing of synaptic populations in multiple contexts. Thus, this project will provide
fundamental knowledge about the synaptic architecture of neurons in the brain. The
由单个神经元执行的计算是整合大量突触输入的结果
分布在复杂的树枝状拓扑结构中。突触输入在很大程度上不同的;感觉驱动的
活动模式、激活概率、突触在树突拓扑中的位置、局部树突
组织和超微结构特征都被认为是决定突触如何
输入会影响神经元的尖峰输出。突触输入的群体,最终决定了
单个神经元可以完成的编码能力和计算能力。尽管如此,研究很大程度上忽略了
单个神经元内的突触输入群体,而不是关注细胞群体的活动,使用
生物物理模型或构建创建假设权重或突触的模型(例如,深层神经
网络)。因此,神经科学中的一个关键问题仍然是如何整合整体突触活动。
以及描述神经计算的突触组织的基本原则是什么。
为了解决这个问题,我们提出了一种紧密结合的实验和理论方法。我们建议(1)
测量第2/3层视觉上大量树突棘的感觉驱动的活动模式
以及(2)使用统计物理方法来表征雪貂视觉皮质的
多语境下突触群体的结构和计算。因此,该项目将提供
关于大脑中神经元突触结构的基础知识。这个
项目成果
期刊论文数量(0)
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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Krishnan Padmanabhan其他文献
Krishnan Padmanabhan的其他文献
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{{ truncateString('Krishnan Padmanabhan', 18)}}的其他基金
in vivo imaging of transplanted human induced-Pluripotent Stem Cell (iPSC) derived neurons to model neurological and psychiatric disorders
对移植的人类诱导多能干细胞 (iPSC) 衍生的神经元进行体内成像,以模拟神经和精神疾病
- 批准号:
9377090 - 财政年份:2017
- 资助金额:
$ 26.13万 - 项目类别:
in vivo imaging of transplanted human induced-Pluripotent Stem Cell (iPSC) derived neurons to model neurological and psychiatric disorders
对移植的人类诱导多能干细胞 (iPSC) 衍生的神经元进行体内成像,以模拟神经和精神疾病
- 批准号:
9895863 - 财政年份:2017
- 资助金额:
$ 26.13万 - 项目类别:
in vivo imaging of transplanted human induced-Pluripotent Stem Cell (iPSC) derived neurons to model neurological and psychiatric disorders
对移植的人类诱导多能干细胞 (iPSC) 衍生的神经元进行体内成像,以模拟神经和精神疾病
- 批准号:
10132398 - 财政年份:2017
- 资助金额:
$ 26.13万 - 项目类别:
ENGRAFTING HUMAN NEURONS INTO ANIMAL MODELS TO STUDY SCHIZOPHRENIA
将人类神经元移植到动物模型中研究精神分裂症
- 批准号:
9233312 - 财政年份:2013
- 资助金额:
$ 26.13万 - 项目类别:
Engrafting human neurons into animal models to study schizophrenia
将人类神经元移植到动物模型中研究精神分裂症
- 批准号:
8727110 - 财政年份:2013
- 资助金额:
$ 26.13万 - 项目类别:
Engrafting human neurons into animal models to study schizophrenia
将人类神经元移植到动物模型中研究精神分裂症
- 批准号:
8568589 - 财政年份:2013
- 资助金额:
$ 26.13万 - 项目类别:
ENGRAFTING HUMAN NEURONS INTO ANIMAL MODELS TO STUDY SCHIZOPHRENIA
将人类神经元移植到动物模型中研究精神分裂症
- 批准号:
9316713 - 财政年份:2013
- 资助金额:
$ 26.13万 - 项目类别:
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