Role of the Notch Pathway in Kidney Injury
Role of the Notch Pathway in Kidney Injury
批准号:
8716732
负责人:
KATALIN SUSZTAK
金额:
$43.34万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-03-01 至 2016-06-30
关键词:
AdultAdverse effectsAffectAgingAnimal ModelArchitectureBindingBiological ProcessCardiovascular systemCell CommunicationCell Differentiation processCell NucleusCell ProliferationCellsChronic Kidney FailureCoculture TechniquesCollagenCommunitiesComplexDataDevelopmentDistalEnd stage renal failureEndothelial CellsEpithelialEpithelial CellsEquilibriumFibroblastsFibrosisFunctional disorderFundingGene Expression ProfileGenetic TranscriptionGenomeGoalsGreen Fluorescent ProteinsHomeostasisIn VitroInflammatoryInjuryIntestinesKidneyLigandsMapsMediatingMedicalModelingMolecularMusMyofibroblastPathway interactionsPatientsPhenotypePlayPrevalenceProtein IsoformsProteinsProteolysisRenal functionResolutionRoleSignal TransductionSolid NeoplasmSystemToxic effectTransgenic MiceTravelTubular formationbasecell typegenome-widein vivoinhibitor/antagonistinterstitialinterstitial cellmortalitynephrogenesisnotch proteinreceptorrepairedresearch studyscreening
中文摘要
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英文摘要
DESCRIPTION (provided by applicant). The primary goal of this proposal is to explore the hypothesis that the Notch pathway plays an important role in the development of chronic kidney disease and kidney fibrosis. We found via large scale genome screening that Notch pathway proteins are regulated in patients and animal models chronic kidney disease and fibrosis. In this application we propose to perform a systematic analysis to examine the role of renal tubular epithelial Notch signaling in the adult kidney at baseline and diseased kidneys. First we will examine whether tubular epithelial Notch signaling plays any role in the adult kidney homeostasis, aging and repair. Next we will analyze which Notch receptor and ligand isoforms is responsible for the renal damage during injury. The third specific aim will define the molecular mechanism of Notch induced epithelial dysfunction and interstitial fibrosis. The current proposal will built on our original observation and explore the role of Notch signaling in the adult kidney both at baseline and in injury models. These studies will help not only deepen our understanding of renal epithelial homeostasis, but also aid the potential development of Notch based inhibitors for chronic kidney disease.
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会议论文
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资助金额:$48.91万
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海外基金