Living Cell Arrays for Real Time Functional Genomics
Living Cell Arrays for Real Time Functional Genomics
批准号:
7433703
负责人:
Martin L Yarmush
金额:
$66.47万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-07-01 至 2010-02-28
关键词:
Acute-Phase ProteinsAcute-Phase ReactionAdultAequorinArtsBindingBiomedical EngineeringBiomedical ResearchCell LineCell physiologyCellsChimeric ProteinsChronicComplexConditionCytokine SignalingDNADevelopmentDevicesDimerizationDisciplineDiseaseDoseEnergy TransferEngineeringEventFOS geneFibrosisFluorescenceFocus GroupsGene ExpressionGene Expression ProfileGene Expression ProfilingGene ProteinsGenesGenetic EngineeringGoldGrowthHepaticHepatocyteImageIn VitroInflammationInflammatoryInflammatory ResponseInjuryInterleukin-6InterleukinsIntracellular Accumulation of LipidsJUN geneLaboratoriesLeadLifeLiverLiver FibrosisLiver diseasesMetabolicMetabolismMethodsMicrofabricationMicrofluidicsMolecularMolecular BiologyMolecular ProfilingMonitorNonesterified Fatty AcidsNumbersOutcomePhenotypePhosphorylase PhosphatasePhosphorylationPhysiologicalPhysiologyPrimary carcinoma of the liver cellsPrincipal InvestigatorProcessProliferatingProtein DephosphorylationProteinsRattusRegulationReporterResearchResearch PersonnelSignal TransductionStandards of Weights and MeasuresSteatohepatitisStimulusStructureSystemTechniquesTechnologyTestingTimeTissuesTranscription Factor AP-1TransfectionTumor Necrosis Factor-alphaTumor Necrosis Factorsbasebody systemchemokineconceptcytokinedata acquisitiondesignfunctional genomicsgene therapyhepatoma cellhuman TNF proteinpromoterresearch studyresponsesuccesstooltranscription factortrend
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): New tools are revolutionizing biomedical research, enabling an exponential growth in the acquisition of data regarding genes, proteins, and their structures and functions in normal and diseased states. Among these advances, the ability to monitor profiles of genes on a large scale is notable. However, it is often difficult to correlate the trends and relationships observed in normal and abnormal states to the phenotype resulting from the gene expression profile. For physiological states involving metabolic derangements, gene expression profiling does not fully explain the complex molecular mechanisms involved. Thus, in order to develop a comprehensive understanding of metabolic states, it is essential to understand both the gene expression events as well as the cytoplasmic events, which control changes in metabolites. The proposed Bioengineering Research Partnership seeks to develop a new functional genomics approach for studying gene expression: the use of intact cells for the simultaneous temporal expression profiling of multiple genes using aequorin-type fluorescent proteins (AFP) in a massively parallel, high throughput format. The specific aims are: (1) to generate and characterize a panel of reporter cell lines that monitors the major events in the inflammatory cytokine signaling cascades; (2) to design a microfluidic system to dynamically control the input stimulus as well as the fluorescent response of an array of primary rat hepatocytes and H35 hepatoma reporter cell lines; (3) to characterize the dynamics of cytokine signal transduction and the impact of steatosis and different metabolic states on the acute phase response of these cells. This project will be carried out by three distinct research groups, which will interact extensively. Dr. Martin Yarmush (MGH), the Principal Investigator, will oversee the Administrative and Technical Core, and lead the Cell Physiology and Imaging group, which will integrate the technologies developed by the other Pl's and carry out the bulk of the cell physiology experiments. Dr. Mehmet Toner, Director of the Microscale Engineering Facility at the MGH, will lead the Microfabrication and Microfluidics group focusing on the development of microfabricated devices. Dr. Jeffrey Morgan (Brown Univ., Providence, RI), a molecular biologist and expert in gene therapy, will lead the Molecular Biology and Cell Analysis group focusing on reporter cell line development.
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财政年份:2012
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资助金额:$22.09万
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依托单位:
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资助金额:$26.25万
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Recellularization of Liver Bioscaffolds
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批准号:8699188
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资助金额:$52.45万
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财政年份:2009
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负责人:Martin L Yarmush
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依托单位:
Recellularization of Liver Bioscaffolds
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批准号:8502653
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项目类别:
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资助金额:$50.62万
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负责人:Martin L Yarmush
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依托单位:
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批准号:8231028
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项目类别:
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资助金额:$3.27万
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财政年份:2009
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负责人:Martin L Yarmush
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依托单位:
Extended Storage of Tissues and Organs in Subzero Environments
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批准号:7691150
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项目类别:
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资助金额:$62.45万
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财政年份:2009
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Recellularization of Liver Bioscaffolds
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依托单位:
Extended Storage of Tissues and Organs in Subzero Environments
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批准号:8292234
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项目类别:
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资助金额:$61.6万
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财政年份:2009
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依托单位:
Extended Storage of Tissues and Organs in Subzero Environments
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批准号:8063666
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项目类别:
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资助金额:$63.36万
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财政年份:2009
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负责人:Martin L Yarmush
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依托单位:
Metabolic Engineering for Improved Liver Function
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批准号:7905588
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项目类别:
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资助金额:$10.01万
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财政年份:2009
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负责人:Martin L Yarmush
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依托单位:
Recellularization of Liver Bioscaffolds
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项目类别:
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资助金额:$41.17万
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财政年份:2009
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负责人:Martin L Yarmush
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依托单位:
Recellularization of Liver Bioscaffolds
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项目类别:
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Extended Storage of Tissues and Organs in Subzero Environments
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项目类别:
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负责人:Martin L Yarmush
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依托单位:
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海外基金