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NEURAL CELL ENGINEERING AND IMAGING CORE

NEURAL CELL ENGINEERING AND IMAGING CORE
神经细胞工程和成像核心
批准号:
10669070
负责人:
KOSTANTIN DOBRENIS
金额:
$18.94万
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
未结题
起止时间:
2021-07-23 至 2026-05-31
关键词:
AddressAnatomyAnimal ExperimentsAnimalsBackBiological AssayBrainCell LineCell SeparationCell modelCellsCognitiveComputer WorkstationsComputer softwareConsultationsCorrelation StudiesCoupledCustomData AnalysesDiseaseDissectionElectrophysiology (science)EmbryoEpigenetic ProcessEquipmentEvaluationExperimental DesignsFacultyFundingGene ExpressionGene TargetingGenerationsGeneticGoalsGrantHumanImageImage AnalysisIn SituIn VitroIndividualInjectionsIntellectual and Developmental Disabilities Research CentersIntellectual functioning disabilityInvestigationInvestmentsLaboratoriesLasersLeadershipMicroscopeMicroscopyModernizationModificationMolecularMonitorMutationNamesNeuronal DifferentiationNeuronsNeurosciencesOrganoidsPatientsPhenotypePhysiologicalPreparationPrintingProductionProductivityProteinsProteomicsProtocols documentationPublicationsQuality ControlRNAResearchResearch PersonnelResearch Project GrantsResolutionResource SharingResourcesSamplingScheduleServicesSliceSpecimenStructureSurveysTherapeutic InterventionTimeTissue EngineeringTissue ModelTissuesTrainingUnited States National Institutes of HealthVertebral columnWorkbasebehavioral phenotypingbrain cellcell preparationcellular engineeringcellular imagingclinical phenotypecollegecomputerized data processingdata acquisitiondesigndifferentiation protocolfetus cellgene therapyhigh end computerhigh standardimage processingimage reconstructionimaging softwarein vivoinduced pluripotent stem cellinnovationinstrumentinterestmouse modelneuralneurogenomicsneuroimagingoptogeneticsreconstructionsynergismtherapeutic evaluationtissue preparationtissue/cell culturetooltranslational studytreatment strategyultra high resolution

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PROJECT SUMMARY/ABSTRACT – (Core D: NCEI Core) The Neural Cell Engineering and Imaging Core (Core D, NCEI) has been a vital component of the Kennedy Center for 30 years, steadily growing in resources and user base, with 70 individuals from 50 IDDRC laboratories utilizing the Core in the last 3 years alone. The NCEI Core consists of 3 major divisions: The Cell and Tissue Engineering Subcore, with facilities and expertise for cell/tissue culture work including primary, embryonic, iPS cells and modern neural differentiation protocols. The Modern Microscopy Subcore, with instruments for tissue sectioning and imaging. And the Analysis and Graphics Subcore, which provides workstations with sophisticated software for deconvolution, quantitative 2D to 5D image analyses and reconstruction, custom software and macros, as well as graphics and printing services. To optimize use of these tools for IDDRC investigators and their trainees, NCEI leadership provides in-depth user consultation, emphasizes well-planned experimental design, and engages in vigilant monitoring of project progress. The Core’s value is extended linkage with expert advisors allowing studies on gene targeting, gene therapy, RNA constructs, optogenetics, electrophysiology, and human ES, iPS and fetal cells, including organoids. Productivity and innovation are also enhanced by interaction with other IDDRC Cores, coordinating, e.g., studies correlating brain cell and anatomic changes with behavioral phenotypes (AP), genetic or epigenetic evaluations on isolated cell subpopulations/single cells (NGEN), and translational studies on reprogrammed cells and iPSC-derived organoids from patients (HCP). Core resources also serve the P50 research project on KDM5C disease by providing imaging and quantitative analyses of changes in gene expression, analysis of neural subtypes and dendritic changes in mouse models, and generating iPS cells/organoids and differentiating neurons from patient samples carrying KDM5C mutations. The Core maintains high standards of quality control through scheduled internal evaluations and the annual user survey carried out by the ADM Core. Collectively, the NCEI Core represents a significant part of the scientific bridge between genetics and cognitive phenotypes and as such has a broad and significant impact on the research carried out by IDDRC investigators and their trainees focused on, and critical to, understanding and treating IDDs.
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