Cellular Imaging Core (CIC)
细胞成像核心 (CIC)
基本信息
- 批准号:10239467
- 负责人:
- 金额:$ 16.11万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2021
- 资助国家:美国
- 起止时间:2021-07-22 至 2026-05-31
- 项目状态:未结题
- 来源:
- 关键词:AddressAdvisory CommitteesAnimal ModelAnimalsArray tomographyAttentionBostonCandidate Disease GeneCellsCollaborationsCommunitiesComplexComputer softwareConsultationsCustomDataData AnalysesDevelopmentDiseaseEducational workshopEquipmentExperimental DesignsFund RaisingFundingFunding AgencyFutureGene ProteinsGoalsGrantImageImage AnalysisImaging TechniquesImaging technologyIn VitroIndividualIntellectual and Developmental Disabilities Research CentersInterdisciplinary StudyKnowledgeLaboratoriesLasersMaintenanceMicroscopeMicroscopyMonitorNeurobiologyNeurodevelopmental DisorderNeurologicNeurologyNeuronsOrganPathologicPediatric HospitalsPlayPopulationPrivatizationProceduresProteinsQuality ControlReproducibility of ResultsResearchResearch PersonnelResolutionResource AllocationResourcesRoleSamplingScanningServicesSignal TransductionSiteStatistical Data InterpretationStructureSystemTechniquesTechnologyTimeTissuesTrainingTraining ProgramsUnited States National Institutes of HealthVendorVisualizationWorkanalysis pipelineanimal imagingawakebasecellular imagingdata acquisitiondesigndigital imagingexperimental studyimaging approachimaging modalityin vivoin vivo imaginginstrumentinstrumentationinterestmedical schoolsmembermicroscopic imagingmultiphoton imagingneurodevelopmentnew technologynoveloptogeneticsprogramsquantitative imaging
项目摘要
ABSTRACT
The Cellular Imaging Core (CIC) plays a pivotal role in the multidisciplinary research pipeline of IDDRC
investigators at Boston Children’s Hospital and Harvard Medical School. Located within the Kirby Neurobiology
Center of Boston Children’s Hospital, this shared microscopy facility offers researchers access to high-end and
specialized microscopy and digital imaging approaches which they can harness to understand the underlying
mechanisms and structural changes associated with neurodevelopmental disorders. The Core offers widefield,
confocal (multiphoton, laser-scanning, spinning disk) and super-resolution (stimulated emission depletion,
STED) microscopes for high resolution subcellular localization of proteins of interest, for tracking live cells over
prolonged periods of time, and for monitoring populations of cells in vivo in an awake, behaving animal. These
instruments are accompanied with access to image analysis workstations, and importantly, to an extensive
educational program that trains researchers one-on-one on the capabilities and limitations of each instrument
and software package used. Core staff can also collaborate closely with IDDRC researchers in core-assisted
projects to design, optimize and implement custom designed experiments or analysis approaches. Additionally,
the Core offers Instrumentation and Technology Courses to inform the scientific community about what is new
for state-of-the-art microscopy, to provide interactive, hands-on workshops on image acquisition, analysis and
processing and to address issues in robustness with these imaging methods. Through these interactions with
researchers, the Core identifies and obtains new equipment and technology that is relevant to our researchers.
Taken together, here the CIC proposes a comprehensive program of collaboration with IDDRC investigators
and other IDDRC Cores to lower the barrier for laboratories to incorporate novel and transformative
microscopy technologies that elevate and accelerate our understanding of normal and pathological neural
development, plasticity and function.
抽象的
细胞成像核心 (CIC) 在 IDDRC 的多学科研究管道中发挥着关键作用
波士顿儿童医院和哈佛医学院柯比神经生物学的研究人员。
这个共享显微镜设施位于波士顿儿童医院中心,为研究人员提供了接触高端和
他们可以利用专门的显微镜和数字成像方法来了解底层
与神经发育障碍相关的机制和结构变化。
共焦(多光子、激光扫描、旋转盘)和超分辨率(受激发射损耗、
STED)显微镜,用于感兴趣蛋白质的高分辨率亚细胞定位,用于跟踪活细胞
长时间,并用于监测清醒、行为动物体内的细胞群。
仪器可以访问图像分析工作站,重要的是,可以访问广泛的
教育计划,对研究人员进行一对一培训,了解每种仪器的功能和局限性
核心人员还可以与 IDDRC 研究人员在核心辅助方面密切合作。
设计、优化和实施定制设计的实验或分析方法的项目。
核心提供仪器和技术课程,向科学界通报最新动态
对于最先进的显微镜,提供有关图像采集、分析和
通过这些成像方法的相互作用来处理并解决鲁棒性问题。
研究人员,核心识别并获得与我们的研究人员相关的新设备和技术。
综上所述,CIC 在此提出了与 IDDRC 调查人员合作的全面计划
和其他 IDDRC 核心,以降低实验室纳入新颖和变革性的障碍
显微镜技术可以提高和加速我们对正常和病理神经的理解
发育、可塑性和功能。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Hisashi Umemori其他文献
Hisashi Umemori的其他文献
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{{ truncateString('Hisashi Umemori', 18)}}的其他基金
Molecular Codes for the Establishment of Functionally Segregated Dopaminergic Circuits
建立功能分离的多巴胺能回路的分子密码
- 批准号:
10415208 - 财政年份:2021
- 资助金额:
$ 16.11万 - 项目类别:
Molecular Codes for the Establishment of Functionally Segregated Dopaminergic Circuits
建立功能分离的多巴胺能回路的分子密码
- 批准号:
10296721 - 财政年份:2021
- 资助金额:
$ 16.11万 - 项目类别:
Molecular Codes for the Establishment of Functionally Segregated Dopaminergic Circuits
建立功能分离的多巴胺能回路的分子密码
- 批准号:
10618351 - 财政年份:2021
- 资助金额:
$ 16.11万 - 项目类别:
Finding the projection-specific dopaminergic synaptic organizers
寻找投射特异性多巴胺能突触组织者
- 批准号:
10162573 - 财政年份:2017
- 资助金额:
$ 16.11万 - 项目类别:
How do neurons in the brain decide to refine their synaptic connections in vivo?
大脑中的神经元如何决定在体内完善其突触连接?
- 批准号:
9383862 - 财政年份:2017
- 资助金额:
$ 16.11万 - 项目类别:
Small Molecule Inhibitors of FGF22-Mediated Excitatory Synaptogenesis & Epilepsy
FGF22 介导的兴奋性突触发生的小分子抑制剂
- 批准号:
8325818 - 财政年份:2012
- 资助金额:
$ 16.11万 - 项目类别:
Small Molecule Inhibitors of FGF22-Mediated Excitatory Synaptogenesis & Epilepsy
FGF22 介导的兴奋性突触发生的小分子抑制剂
- 批准号:
8792428 - 财政年份:2012
- 资助金额:
$ 16.11万 - 项目类别:
Synapse Maturation by Activity-Dependent Ectodomain Shedding of SIRP
SIRP 活性依赖性胞外域脱落导致突触成熟
- 批准号:
8026981 - 财政年份:2011
- 资助金额:
$ 16.11万 - 项目类别:
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