CORE--Imaging and Physiology Core
CORE--影像与生理学核心
基本信息
- 批准号:7367826
- 负责人:
- 金额:$ 26.99万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2007
- 资助国家:美国
- 起止时间:2007-03-01 至 2010-02-28
- 项目状态:已结题
- 来源:
- 关键词:AddressAlbuminsAreaBlood VesselsCellsConfocal MicroscopyDNADrug FormulationsElectron MicroscopyEndothelial CellsEquipmentFiltrationFluorescence MicroscopyGenesGoalsHuman ResourcesImageImage AnalysisIndividualIntercellular JunctionsLiposomesLungMeasurementMethodsMusPathway interactionsPermeabilityPhysiologicalPhysiologyProceduresResourcesSurfaceTechnical ExpertiseTrainingTransfectionVascular Permeabilitiesexperienceinterestmonolayer
项目摘要
The goal of Core D: Imaging and Physiology Core, is to provide technical support, expertise, and resources for electron microscopy, fluorescence & confocal microscopy, image analysis, and mouse lung vascular permeability measurements that will be required to address the specific aims of all projects. The centralization of the imaging and physiological support within Core D is necessitated by the emphasis of the individual projects on the physiological relevance of the proposed studies. Thus, Core D will provide equipment and technical expertise for carrying out and analyzing the functional studies in mouse lungs or endothelial cell monolayers. In this context, Core D will provide expertise and technical support for studying the permeability of lung vascular endothelial barrier using physiological methods (i.e., pulmonary microvessel filtration coefficient and vessel wall albumin permeability surface area product) as well as examination of specific permeability pathways using electron microscopy and quantitative image analysis at
the level of cell-cell junctions and transcellular pathway. All Projects will require assessments of lung vascular permeability provided by Core D. Core D will also provide expertise for the formulation of DNA containing cationic liposomes and the transfection of genes of interest in mouse lung microvessels. Core D personnel, who have extensive training and experience in the described procedures, will provide the support and resources outlined below as well as
the necessary training of personnel in all Projects.
核心D的目标:成像和生理学核心,是提供技术支持,专业知识和资源,电子显微镜,荧光和共聚焦显微镜,图像分析和小鼠肺血管通透性测量,将需要解决所有项目的具体目标。核心D内的成像和生理支持的集中化是必要的,因为单个项目强调了拟议研究的生理相关性。因此,核心D将提供设备和技术专长,用于在小鼠肺或内皮细胞单层中进行和分析功能研究。在此背景下,核心D将为使用生理方法研究肺血管内皮屏障的通透性提供专业知识和技术支持(即,肺微血管滤过系数和血管壁白蛋白渗透性表面积乘积)以及使用电子显微镜和定量图像分析在
细胞间连接和跨细胞通路水平。所有项目都需要由核心D提供肺血管通透性评估。核心D还将提供含有阳离子脂质体的DNA制剂和小鼠肺微血管中感兴趣基因转染的专业知识。核心D人员在所述程序方面接受过广泛培训并具有丰富经验,他们将提供下述支持和资源,
对所有项目的人员进行必要的培训。
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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RICHARD D MINSHALL其他文献
RICHARD D MINSHALL的其他文献
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{{ truncateString('RICHARD D MINSHALL', 18)}}的其他基金
Fibroblast Mediated Mechanisms of Pulmonary Hypertension
成纤维细胞介导的肺动脉高压机制
- 批准号:
10163897 - 财政年份:2019
- 资助金额:
$ 26.99万 - 项目类别:
Fibroblast Mediated Mechanisms of Pulmonary Hypertension
成纤维细胞介导的肺动脉高压机制
- 批准号:
10378641 - 财政年份:2019
- 资助金额:
$ 26.99万 - 项目类别:
Fibroblast Mediated Mechanisms of Pulmonary Hypertension
成纤维细胞介导的肺动脉高压机制
- 批准号:
10599245 - 财政年份:2019
- 资助金额:
$ 26.99万 - 项目类别:
Fibroblast Mediated Mechanisms of Pulmonary Hypertension
成纤维细胞介导的肺动脉高压机制
- 批准号:
9912845 - 财政年份:2019
- 资助金额:
$ 26.99万 - 项目类别:
Src Regulation of Lung Endothelial Barrier Function
Src 对肺内皮屏障功能的调节
- 批准号:
8059132 - 财政年份:2011
- 资助金额:
$ 26.99万 - 项目类别:
Caveolin-1 and NO Regulate PMN-mediated Increases in Vascular Permeability
Caveolin-1 和 NO 调节 PMN 介导的血管通透性增加
- 批准号:
7822536 - 财政年份:2009
- 资助金额:
$ 26.99万 - 项目类别:
Src Regulation of Lung Endothelial Barrier Function
Src 对肺内皮屏障功能的调节
- 批准号:
7367823 - 财政年份:2007
- 资助金额:
$ 26.99万 - 项目类别:
Src Regulation of Lung Endothelial Barrier Function
Src 对肺内皮屏障功能的调节
- 批准号:
7312502 - 财政年份:2006
- 资助金额:
$ 26.99万 - 项目类别:
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