System for advanced automated 3D microvascular analysis in neuroplasticity
System for advanced automated 3D microvascular analysis in neuroplasticity
批准号:
9332468
负责人:
Paul Angstman
金额:
$49.99万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-09-06 至 2019-07-31
关键词:
AddressAgingAlgorithmsBiologicalBiomedical ResearchBiotechnologyBlood VesselsBrainBrain DiseasesCollaborationsCommunitiesComplexComputer softwareDestinationsDevelopmentDimensionsEncephalitisGrantGraphImageImage AnalysisLearningLightLightingManualsMarketingMental HealthMental disordersMichiganMicroscopeMicroscopicNational Institute of Mental HealthNerve DegenerationNeuronal PlasticityNeuronsNeurosciencesNeurosciences ResearchNew YorkOpticsPathologicPerformancePeriodicityPharmacologyPhasePhysiologicalPlayProcessProductionReportingReproducibilityResearchResearch PersonnelRoleScientistSmall Business Innovation Research GrantSocietiesSoftware ToolsStructureSynaptic plasticitySystemSystems AnalysisTechniquesTechnologyTestingThree-Dimensional ImageThree-dimensional analysisTimeTissuesTraumatic Brain Injury recoveryTreesUnited States National Institutes of HealthUniversitiesValidationadvanced systembrain morphologybrain tissuecerebral microvasculaturecommercializationdata modelingdigitalexperiencefightingimprovedinnovationinsightmedical schoolsmicroscopic imagingmigrationnetwork modelsneurogenesisnovelresearch and developmenttechnology developmenttherapeutic developmenttooltreatment strategytwo-photonusability
中文摘要
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英文摘要
Abstract
It has become evident that the microvasculature (i.e., microscopically small blood vessels) plays a critical role in
the plasticity of the brain for fundamental processes: (i) neurogenesis, (ii) migration of neuronal precursors to
their final destination in the brain, (iii) axonal, dendritic and synaptic plasticity during brain development, learning,
aging and neurodegeneration, and (iv) recovery from traumatic brain injury and brain inflammation. For more
than thirty years, investigators have attempted to trace, reconstruct, visualize and quantitatively characterize the
three-dimensional (3D) morphology of the brain's microvasculature in normal and pathological tissue (3D
microangioarchitectonics). Yet, 3D microangioarchitectonics is rarely used in neuroscience research due to the
paucity of adequate tools. The investigators who have started to study 3D microangioarchitectonics use software
tools that were developed for other purposes. Because these software tools make use of data models which are
inappropriate for 3D microangioarchitectonics and have not been validated against a manually established
ground truth, the results must be considered faulty and irreproducible. To remedy this untenable situation we
propose to create Vesselucida, an innovative software product to perform advanced, accurate and reproducible
automatic 3D microangioarchitectonics in normal and pathological brain tissue. This software will allow significant
advancements in (i) neuroscience research that addresses the roles of microvessels on various aspects of
neuroplasticity, and (ii) pharmacological and biotechnology research and development. These advancements
will be the basis for the development of innovative treatments to fight complex brain diseases. During Phase I
we successfully established proof of concept and demonstrated that the development of Vesselucida represents
substantial progress beyond the state-of-the-art, with great benefits for the neuroscience research community
and society in general.
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海外基金