Anatomical characterization of neuronal cell types of the mouse brain
Anatomical characterization of neuronal cell types of the mouse brain
批准号:
10262970
负责人:
GIORGIO A ASCOLI
金额:
$258.26万
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:
2020-07-29 至 2024-05-31
关键词:
3-DimensionalAlgorithmsAnatomyAtlasesAxonBRAIN initiativeBrainCatalogsCellsCellular MorphologyCensusesCharacteristicsClassificationContralateralCustomDataDiseaseElectrophysiology (science)FLP recombinaseFoundationsGeneticGoalsHealthHealth systemImageIndividualInformaticsInjectionsIntuitionIpsilateralKnowledgeLabelLaboratoriesLimbic SystemLiteratureLocationMapsMetadataMethodsMicroscopyMonstersMorphologyMusNeuronsOnline SystemsOrganizational ProductivityOutcomeOutputPatternProcessProteinsPublishingRabiesRabies virusResolutionResourcesSiteStructureSubcellular AnatomySynapsesTechnologyTissuesViralVirusVisualizationVisualization softwarebasecell typecollaboratorydesignexperimental studyhigh resolution imaginginformatics toolmicroscopic imagingmotivated behaviormultiphoton imagingnovelnovel strategiesrabies viral tracingreconstructionrepositoryresponseserial imagingtoolweb interface
中文摘要
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英文摘要
PROJECT SUMMARY AND ABSTRACT
A comprehensive understanding neuronal cell type diversity is an essential guide to selective manipulation and
illuminating cell type specific functional contributions toward health and disease. Accordingly, the Brain
Initiative Cell Census Network (BICCN) is unifying the efforts of laboratories with unique expertise in anatomy,
genetics, electrophysiology, and function to classify neurons and create a common 3D atlas with integrated cell
type data. To this end, our proposed collaboratory aims to anatomically characterize neuronal cell types of the
mouse limbic system. Using mesoscale quadruple retrograde tracing, we will initially characterize cell types
based on the anatomical location of their connectional start and end points [e.g.,
ACB(contralateral)←BLAa→ACB(ipsilateral)]. A two-step cre-dependent AAV tracing strategy using advanced
viral tools will subsequently validate and refine specific axonal projections, collaterals, and projection fields
[e.g., ACB/X/Y←BLAa→ACB/X/Y]. Injections of G-deleted rabies in CLARITY-processed tissue will label
morphological features of cell types. Cre-dependent TRIO viral tracing will determine discrete inputs to each
cell type, providing deeper characterization of connectivity. Novel TRIO using flp recombinase in cre-
dependent mice will define projection patterns of genetically-defined cell types. Newly constructed AAV and
rabies viruses tagged to spaghetti monster fluorescent proteins, applied in combination with Expansion
Microscopy and multiphoton imaging, will determine the spatial organization of different synaptic inputs to the
cell types. Collectively, experiments will reveal cell type anatomic location, morphology, and comprehensive
connectivity. Initial efforts will focus on the limbic system, with the design extensible to neuronal
characterization of the entire brain. A web-based visualization platform will be developed to enable viewing and
analysis of cell type anatomy data in 2D and 3D. An online visualization tool similar in function to our
iConnectome viewer will present quadruple retrograde and TRIO tracing images. Digitized, reconstructed
quadruple retrograde, cre-AAV, and TRIO labeling will be placed atop the Allen Reference Atlas (ARA) to
create an online 2D connectivity map, allowing easy comparison of cell type specific inputs and outputs.
Common Coordinate Framework (CCF) registration and reconstruction of cre-AAV labeling experiments will
provide the cell type specific 3D context of projections, with input and morphological information integrated into
the viewer. An interactive, weighted and directed matrix will present an intuitive visualization of all connectivity
data. 3D reconstructed neurons will also be hosted on Neuromorpho.org for interspecies comparison. Our
current informatics pipelines will be extended and optimized to support the proposed viewer features. We
expect our technologies to elucidate diverse cell type specific networks and provide foundations for the
overarching goal of the BICCN of creating a comprehensive 3D cell type atlas.
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Third-generation rabies viral vectors allow nontoxic retrograde targeting of projection neurons with greatly increased efficiency.
第三代狂犬病病毒载体允许效率提高的投射神经元逆行逆行靶向。
DOI:
10.1016/j.crmeth.2023.100644
发表时间:
2023-11-20
期刊:
Cell reports methods
影响因子:
--
作者:
[Jin L, Sullivan HA, Zhu M, Lea NE, Lavin TK, Fu X, Matsuyama M, Hou Y, Feng G, Wickersham IR]
通讯作者:
Wickersham IR
DOI:
10.1073/pnas.2023481120
发表时间:
2023-02-14
期刊:
Proceedings of the National Academy of Sciences of the United States of America
影响因子:
11.1
作者:
[]
通讯作者:
DOI:
10.1002/cne.24966
发表时间:
2021-03
期刊:
The Journal of comparative neurology
影响因子:
--
作者:
[Hahn JD, Swanson LW, Bowman I, Foster NN, Zingg B, Bienkowski MS, Hintiryan H, Dong HW]
通讯作者:
Dong HW
DOI:
10.1016/j.pbb.2017.12.010
发表时间:
2018-11
期刊:
Pharmacology, biochemistry, and behavior
影响因子:
--
作者:
[Knowland D, Lim BK]
通讯作者:
Lim BK
Long-range neuronal projections: circuit blueprint or stochastic targeting? Rigorous classification of brain-wide axonal reconstructions
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批准号:10360723
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项目类别:
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资助金额:$128.71万
-
财政年份:2021
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负责人:GIORGIO A ASCOLI
-
依托单位:
Anatomical characterization of neuronal cell types of the mouse brain
-
批准号:10225863
-
项目类别:
-
资助金额:$266.05万
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财政年份:2020
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负责人:GIORGIO A ASCOLI
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依托单位:
Anatomical characterization of neuronal cell types of the mouse brain
-
批准号:9567222
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项目类别:
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资助金额:$272.83万
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财政年份:2017
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负责人:GIORGIO A ASCOLI
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依托单位:
Cytoskeletal mechanisms of dendrite arbor shape development
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批准号:10649463
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项目类别:
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资助金额:$30.13万
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财政年份:2013
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负责人:GIORGIO A ASCOLI
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依托单位:
Cytoskeletal mechanisms of dendrite arbor shape development
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批准号:10162670
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项目类别:
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资助金额:$30.13万
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财政年份:2013
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负责人:GIORGIO A ASCOLI
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依托单位:
Cytoskeletal mechanisms of dendrite arbor shape development
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批准号:10404546
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项目类别:
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资助金额:$30.13万
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财政年份:2013
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负责人:GIORGIO A ASCOLI
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依托单位:
Reconstruction and Mapping of Human Brain Vasculature
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批准号:7860671
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项目类别:
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资助金额:$20.16万
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财政年份:2009
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负责人:GIORGIO A ASCOLI
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依托单位:
Neuroinformatics of the Hippocampus: From System-Level to Neuronal Arborizations
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批准号:7532436
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项目类别:
-
资助金额:$15.19万
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财政年份:2008
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负责人:GIORGIO A ASCOLI
-
依托单位:
ANATOMICALLY ACCURATE NEURAL NETWORKS: BUILDING A HIPPOCAMPUS
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批准号:7369377
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项目类别:
-
资助金额:$1.02万
-
财政年份:2006
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负责人:GIORGIO A ASCOLI
-
依托单位:
ANATOMICALLY ACCURATE NEURAL NETWORKS: BUILDING A HIPPOCAMPUS
-
批准号:7182786
-
项目类别:
-
资助金额:$0.98万
-
财政年份:2005
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负责人:GIORGIO A ASCOLI
-
依托单位:
CRCNS: Input/Output Relationship in CA3 Pyramidal Cells
-
批准号:6951044
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项目类别:
-
资助金额:$30.26万
-
财政年份:2004
-
负责人:GIORGIO A ASCOLI
-
依托单位:
CRCNS: Input/Output Relationship in CA3 Pyramidal Cells
-
批准号:7474611
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项目类别:
-
资助金额:$29.04万
-
财政年份:2004
-
负责人:GIORGIO A ASCOLI
-
依托单位:
CRCNS: Input/Output Relationship in CA3 Pyramidal Cells
-
批准号:6887559
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项目类别:
-
资助金额:$31.2万
-
财政年份:2004
-
负责人:GIORGIO A ASCOLI
-
依托单位:
CRCNS: Input/Output Relationship in CA3 Pyramidal Cells
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批准号:7102590
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项目类别:
-
资助金额:$30.43万
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财政年份:2004
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负责人:GIORGIO A ASCOLI
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依托单位:
CRCNS: Input/Output Relationship in CA3 Pyramidal Cells
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批准号:7255435
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项目类别:
-
资助金额:$28.88万
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财政年份:2004
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负责人:GIORGIO A ASCOLI
-
依托单位:
ANATOMICALLY ACCURATE NEURAL NETWORKS:A HIPPOCAMPUS
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批准号:6978970
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项目类别:
-
资助金额:$2.75万
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财政年份:2004
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负责人:GIORGIO A ASCOLI
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依托单位:
GENERATION AND DESCRIPTION OF DENDRITIC MORPHOLOGY
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批准号:6529430
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项目类别:
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资助金额:$10.93万
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财政年份:1999
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负责人:GIORGIO A ASCOLI
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依托单位:
Generation and Description of Neuronal Morphology and Connectivity
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批准号:8066283
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项目类别:
-
资助金额:$29.23万
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财政年份:1999
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负责人:GIORGIO A ASCOLI
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依托单位:
Generation and Description of Neuronal Morphology and Connectivity
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批准号:10613429
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项目类别:
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资助金额:$36.9万
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财政年份:1999
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负责人:GIORGIO A ASCOLI
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依托单位:
Generation and Description of Dendritic Morphology
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批准号:7233290
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项目类别:
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资助金额:$31.21万
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财政年份:1999
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负责人:GIORGIO A ASCOLI
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依托单位:
海外基金