Understanding overlap in resting state fMRI networks at the single cell level: a cross-species approach
Understanding overlap in resting state fMRI networks at the single cell level: a cross-species approach
批准号:
10059107
负责人:
Janine Diane Bijsterbosch
金额:
$70.88万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-08-15 至 2023-05-31
关键词:
AddressAffectAnimal ModelAnimalsArchitectureBehaviorBiologicalBrainCellsCognitionCognitiveCognitive deficitsCollaborationsCouplingDataElectrodesElectrophysiology (science)Functional Magnetic Resonance ImagingHumanImage AnalysisIndividualInterdisciplinary StudyInvestigationLesionLife StyleLinkLocationMacacaMagnetic Resonance ImagingMeasurementMental ProcessesMethodologyMethodsMicroelectrodesModelingMonkeysNeuronsOutcomeOxygenParietal LobePatternPlayPolarographyPrimatesResolutionRestRoleSignal TransductionSiteStructureTechniquesTestingTimeTissuesVariantanalytical methodawakebasebehavior testblood oxygen level dependentexperimental studyfollow-upforgingimagerinterdisciplinary collaborationinterestneural circuitnonhuman primatenovelrelating to nervous systemtool
中文摘要
在单细胞水平上理解静息状态fMRI网络的重叠:一个跨物种的研究
方法
摘要
静息态功能连接MRI(rsfcMRI)是研究脑内神经元功能的常用工具。
将大脑的功能组织成大规模的网络。多条不同的
调查指出了密集互联的“枢纽”区域的重要性,
认知和行为。然而,这些中枢中的细胞电路的功能架构
地区不详。为了研究枢纽区域的细胞基础,我们将一个
跨学科的研究团队,跨越物种和跨越规模的桥梁。我们首先
概括了人类fcMRI分析在不同物种中的最新进展,
清醒猕猴rsfcMRI数据中网络重叠的个体化模式(Aim
1)。这使我们能够从集线器中识别相同动物的记录的感兴趣区域
两个(或多个)网络在空间上重叠的区域,以及两个
分别对其中一个网络有很大贡献。然后我们问,在一个更好的
在细胞尺度上,枢纽区域的两个网络之间存在真正的神经耦合,或者
在rsfcMRI数据的分辨率下出现空间重叠的网络实际上在空间上是重叠的。
在更精细的尺度上相互交叉而不是重叠(目标2)。最后,我们使用电生理学
记录以确定中枢区域中的单个神经元是否整合来自
重叠网络(即耦合),或者神经元是否动态切换其网络
随着时间的推移,从一个网络到另一个网络的忠诚度(目标3)。该提案的成果包括:
对人类rsfcMRI数据的建模和解释具有重要意义。R34
提案提供了建立新的合作和验证我们的方法的机会
跨越物种。这些因素对于我们项目的下一个阶段--目标大脑--至关重要
电路项目R 01提案,在该提案中,我们将在此调查基础上,
行为,以研究中枢区域大脑回路的基本原理如何形成
心理过程的生物学基础。
英文摘要
Understanding overlap in resting state fMRI networks at the single cell level: a cross-species
approach
Abstract
Resting state functional connectivity MRI (rsfcMRI) is a popular tool to investigate the intrinsic
functional organization of the brain into large scale networks. Multiple different lines of
investigation have pointed to the importance of densely interconnected `hub' regions for
cognition and behavior. However, the functional architecture of cellular circuits in these hub
regions is unknown. To study the cellular underpinnings of hub regions, we bring together an
interdisciplinary research team to bridge across species and across scales. We start by
generalizing recent advances in human fcMRI analyses across species to characterize
individualized patterns of network overlap in rsfcMRI data from awake macaque monkeys (Aim
1). This allows us to identify regions of interest for recordings in this same animals from a hub
region where two (or more) networks spatially overlap, and from two non-hub regions that
strongly contribute to only one of the networks respectively. We then ask whether, at a finer
cellular scale, there is true neural coupling between both networks in hub regions, or whether
networks that appear spatially overlapping at the resolution of rsfcMRI data are in fact spatially
interdigitated rather than overlapping at a finer scale (Aim 2). Lastly, we use electrophysiological
recordings to determine whether individual neurons in hub regions integrate information from
both overlapping networks (i.e. coupling), or whether neurons dynamically switch their network
allegiance from one network to another over time (Aim 3). The outcomes of this proposal have
important implications for the modeling and interpretation of human rsfcMRI data. This R34
proposal provides the opportunity to establish a new collaboration and validate our methodology
across species. These factors are essential for the next stage of our project, a Targeted Brain
Circuits Project R01 proposal, in which we will build on this line of investigation by bridging into
behavior to study how fundamental principles of the brain circuits in hub regions form the
biological basis of mental processes.
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DOI:
10.1016/j.neuroimage.2021.118513
发表时间:
2021-11
期刊:
NeuroImage
影响因子:
5.7
作者:
[Farahibozorg SR, Bijsterbosch JD, Gong W, Jbabdi S, Smith SM, Harrison SJ, Woolrich MW]
通讯作者:
Woolrich MW
DOI:
10.1002/hbm.25690
发表时间:
2022-02-01
期刊:
Human brain mapping
影响因子:
4.8
作者:
[Dutt RK, Hannon K, Easley TO, Griffis JC, Zhang W, Bijsterbosch JD]
通讯作者:
Bijsterbosch JD
DOI:
10.1038/s41398-022-02172-w
发表时间:
2022-10-03
期刊:
TRANSLATIONAL PSYCHIATRY
影响因子:
6.8
作者:
[Zhang, Wei, Paul, Sarah E., Winkler, Anderson, Bogdan, Ryan, Bijsterbosch, Janine D.]
通讯作者:
Bijsterbosch, Janine D.
DOI:
10.1038/s41593-022-01058-w
发表时间:
2022-06
期刊:
NATURE NEUROSCIENCE
影响因子:
25
作者:
[Bijsterbosch, Janine]
通讯作者:
Bijsterbosch, Janine
HCP-2.0: Ascertaining Network Mechanisms and Analytics of Emotional Dysfunction (HARMONY)
-
批准号:10803654
-
项目类别:
-
资助金额:$84.64万
-
财政年份:2023
-
负责人:Janine Diane Bijsterbosch
-
依托单位:
Individualized brain biomarkers of late life depression: contributions to heterogeneity and resilience
-
批准号:10676995
-
项目类别:
-
资助金额:$46.44万
-
财政年份:2022
-
负责人:Janine Diane Bijsterbosch
-
依托单位:
海外基金