Tissue regulation of T cell function - Imaging Core
Tissue regulation of T cell function - Imaging Core
批准号:
10689176
负责人:
Minsoo Kim
金额:
$44.87万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-06-01 至 2024-08-31
关键词:
3-DimensionalAdhesionsAnimal ModelAnimalsBiologicalCell CommunicationCell Culture TechniquesCell physiologyCellsCollaborationsColorCommunicationComputer softwareComputing MethodologiesCustomDataData AnalysesData Storage and RetrievalDevelopmentDimensionsDiscriminationEarEnvironment DesignEquipmentFluorescenceFosteringGenerationsGoalsHealth SciencesHigh Performance ComputingHousingHuman ResourcesImageImage AnalysisImaging TechniquesImaging technologyImmuneImmune responseImmune systemImmunologic SurveillanceIn SituInfectionInflammationInnate Immune ResponseKnock-in MouseLabelLeukocytesLungLymphoidMaintenanceMethodologyMicroscopyMissionModelingModificationMusProteinsProtocols documentationReactionReagentResearchResearch PersonnelScientistServicesSignal TransductionSiteSkinSmall IntestinesStandardizationSystemT cell regulationT-LymphocyteTechniquesTimeTissue imagingTissuesTracheaTrainingUniversitiesadaptive immune responseanimal imagingcell typechemokine receptorcomputing resourcesdata standardsdesigndigitaleffector T cellexperienceexperimental studyimage processingimaging capabilitiesimaging softwareimaging studyimaging systemimmune functionimprovedin vivoin vivo imagingin vivo imaging systeminformation organizationinnovationintravital microscopylymph nodesmigrationmulti-photonmultiphoton microscopynovelpathogenphotoactivationprogramstool
中文摘要
点击翻译按钮获取中文摘要
英文摘要
PROJECT SUMMARY/ABSTRACT – IMAGING CORE
The host response to pathogen infections is not confined to a single tissue, thus maintenance of homeostatic
immune surveillance and the development of protective immune responses require that cells in the immune
system constantly patrol the entire body, efficiently crossing multiple tissue barriers. Furthermore, in their target
sites, immune cells often have to find customized tissue-specific solutions to effectively identify and eradicate
pathogens. As such, the direct observation of leukocyte adhesion, migration and communication in lymphoid
and non-lymphoid tissues with microscopy is one of the most important experimental approaches. The Imaging
Core (Core B) has been established based on a stated need of PPG investigators and is designed to draw on
the considerable experience of its key personnel to provide expertise and specialized equipment in the design
and execution of in vivo imaging studies of effector T cell functions in infected tissues. The main missions of
the Imaging Core are as follows: 1. To provide state-of-the-art imaging capabilities in conducting specific
experiments regarding leukocyte adhesion and migration as well as cell-cell interactions during local immune
responses in as many as six dimensions (i.e. 3D-space, time, color, fluorescence signals). 2. To develop a
novel hyperspectral multiphoton microscopy for multicellular in vivo imaging. 3. To provide technical assistant
for analysis of the collected image data. 4. To provide assistance in the planning of in vivo animal studies by
offering standardized infectious/inflammation models and a custom-designed environment with appropriate
biosafety conditions for the generation, housing and intravital microscopy analysis of live cell cultures,
explanted tissues, and infected mice. The Cores have already been highly effective in achieving some of these
goals by providing service that both facilitates research and fosters collaborations between investigators, and
by enabling development of novel in vivo animal models and imaging techniques.
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会议论文
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批准号:10515703
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财政年份:2022
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批准号:10643889
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批准号:10084273
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Visualizing the resolution of innate immune responses during influenza infection
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批准号:9899365
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资助金额:$23.1万
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Identification of a Damaging Subset of Neutrophils that Arises in Septic Patients
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批准号:10179456
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资助金额:$50.4万
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T cell migration and cardiovascular toxicity in immunotherapy
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批准号:10646491
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资助金额:$56.94万
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财政年份:2019
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负责人:Minsoo Kim
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依托单位:
T cell migration and cardiovascular toxicity in immunotherapy
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批准号:9981638
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项目类别:
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资助金额:$56.94万
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财政年份:2019
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负责人:Minsoo Kim
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依托单位:
Optical control of T cell metabolism
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批准号:9910585
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项目类别:
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资助金额:$21.6万
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财政年份:2019
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负责人:Minsoo Kim
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依托单位:
T cell migration and cardiovascular toxicity in immunotherapy
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批准号:9814149
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项目类别:
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资助金额:$56.94万
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财政年份:2019
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负责人:Minsoo Kim
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依托单位:
T cell migration and cardiovascular toxicity in immunotherapy
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批准号:10437785
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项目类别:
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资助金额:$56.94万
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财政年份:2019
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负责人:Minsoo Kim
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依托单位:
T cell migration and cardiovascular toxicity in immunotherapy
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批准号:10192644
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项目类别:
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资助金额:$56.94万
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财政年份:2019
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负责人:Minsoo Kim
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依托单位:
Identification of a Damaging Subset of Neutrophils that Arises in Septic Patients
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批准号:10418694
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项目类别:
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资助金额:$50.4万
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财政年份:2019
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负责人:Minsoo Kim
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依托单位:
Optogenetic immunomodulation for adoptive cell transfer therapy
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批准号:9059681
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资助金额:$16.69万
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财政年份:2015
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负责人:Minsoo Kim
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依托单位:
Resolution of neutrophil response for effective T cell functions and tissue repair
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批准号:10002194
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项目类别:
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资助金额:$38.51万
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财政年份:2014
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负责人:Minsoo Kim
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依托单位:
Tissue regulation of T cell function - Imaging Core
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批准号:10477317
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项目类别:
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资助金额:$42.42万
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财政年份:2014
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负责人:Minsoo Kim
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依托单位:
Neutrophil-endothelial interactions and barrier function in sepsis
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批准号:8799334
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项目类别:
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财政年份:2014
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负责人:Minsoo Kim
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依托单位:
Tissue regulation of T cell function - Imaging Core
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批准号:10002191
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项目类别:
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资助金额:$42.67万
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财政年份:2014
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依托单位:
Neutrophil-endothelial interactions and barrier function in sepsis
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批准号:8928645
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项目类别:
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资助金额:$74.64万
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财政年份:2014
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负责人:Minsoo Kim
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依托单位:
海外基金