Signaling mechanisms and functions related to patho-physiology of vascular, lung and blood systems
Signaling mechanisms and functions related to patho-physiology of vascular, lung and blood systems
批准号:
10089468
负责人:
Dianqing Wu
金额:
$91.23万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-02-01 至 2024-01-31
关键词:
Adult Respiratory Distress SyndromeApplications GrantsBiochemicalBiologicalBloodBlood VesselsCRISPR/Cas technologyCell PolarityCell membraneCell-Matrix JunctionCellsChemicalsChemotactic FactorsDiseaseExocytosisFibroblastsFunctional disorderFundingFunding MechanismsG-Protein-Coupled ReceptorsGenomicsHeartIn VitroLaboratoriesLungMediatingMissionMolecularNADPH OxidasePathogenicityPathway interactionsPhysiologicalProcessProteomicsPulmonary FibrosisRNA InterferenceReadinessRegulationResearchResearch Project GrantsSignal PathwaySignal TransductionStructureSystemTechnologyTestingTherapeuticTransgenic OrganismsWnt proteinsbasefallsflexibilityfunctional genomicshigh rewardhigh riskin vivoinnovationinsightinterestmigrationnovelreceptorsuccesstherapeutic target
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Project Summary:
My laboratory is interested in understanding molecular basis and functions for two signaling
pathways that use seven transmembrane receptors in their signaling transduction. One of the
pathways is mediated by G protein-coupled receptors, and the other is activated by Wnt
proteins. We have been using a combination of biochemical, molecular and cell biological,
transgenic, genomic, proteomic, structural and chemical biological approaches to discover novel
signaling mechanisms and investigate their functions in vitro and in vivo. In this R35 application,
I intend to streamline our current four research projects that are pertinent to NHBLI missions
under one funding mechanism. Two of the projects are current funded by NHBLI. These four
projects are: 1) To test the hypothesis that the initial break of the symmetry may arise from PM
PI4P polarization caused by plasma membrane deformation as the result of cell attachment.
Polarized PM PI4P defines the “uropod” and thus the initial cellular polarity, upon which further
polarization stimulated by chemoattractants is extended. 2) To investigate the sustained
signaling pathway for regulation of fibroblast migration and its therapeutic potential in treating
pulmonary fibrosis. 3) To Investigate the hypothesis that increased exocytosis is a pathogenic
basis for CCM disease. 4) To investigate MEKK3 as being a negative regulator of NADPH
oxidase 2 (NOD2) and potential therapeutic target for acute respiratory distress syndrome.
Each of the project is highly innovative and would exert a strong impact in their respective field.
In addition, we are generating the new leads coming from these high risk/high reward studies
that include functional genomic screens based on the CRISPR/Cas9 and RNAi technologies.
Thus, this R35 mechanism would not only allow streamlining our grant application and
management so that we can better focus our effort on research, but also afford us the flexibility
to fully and efficiently pursue the new leads coming from these high risk/high reward studies.
Our track record strongly indicates our readiness, capability, and success to pursue subjects
that we deem to be of high-impact even though they fall outside our initial intents.
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科研奖励(0)
会议论文
A novel signaling mechanism for LRP5
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批准号:10706591
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项目类别:
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资助金额:$53.56万
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财政年份:2022
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负责人:Dianqing Wu
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依托单位:
A novel signaling mechanism for LRP5
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批准号:10527478
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项目类别:
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资助金额:$54.65万
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财政年份:2022
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负责人:Dianqing Wu
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依托单位:
Signaling mechanisms and functions related to patho-physiology of vascular, lung and blood systems
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批准号:9244290
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项目类别:
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资助金额:$91.23万
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财政年份:2017
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负责人:Dianqing Wu
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依托单位:
DKK2 regulates NK activation and tumor immunity
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批准号:10064071
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资助金额:$51.33万
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财政年份:2017
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负责人:Dianqing Wu
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依托单位:
Signaling mechanisms and functions related to patho-physiology of vascular, lung and blood systems
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批准号:10570974
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项目类别:
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资助金额:$91.23万
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财政年份:2017
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负责人:Dianqing Wu
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依托单位:
DKK2 regulates NK activation and tumor immunity
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批准号:10307994
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项目类别:
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资助金额:$50.3万
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财政年份:2017
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负责人:Dianqing Wu
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依托单位:
Sustained signaling for fibroblast migration
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批准号:9066227
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项目类别:
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资助金额:$41.63万
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财政年份:2013
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负责人:Dianqing Wu
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依托单位:
Sustained signaling for fibroblast migration
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批准号:8594750
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项目类别:
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资助金额:$39.63万
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财政年份:2013
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负责人:Dianqing Wu
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依托单位:
Sustained signaling for fibroblast migration
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批准号:8707850
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项目类别:
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资助金额:$40.79万
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财政年份:2013
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负责人:Dianqing Wu
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依托单位:
Identification of novel genes as being important for neutrophil functions
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批准号:8415495
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项目类别:
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资助金额:$20.79万
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财政年份:2012
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负责人:Dianqing Wu
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依托单位:
Identification of novel genes as being important for neutrophil functions
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批准号:8300322
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项目类别:
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资助金额:$24.87万
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财政年份:2012
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负责人:Dianqing Wu
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依托单位:
Signaling Mechanisms for Leukocyte Migration Regulation
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批准号:8199731
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项目类别:
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资助金额:$48.9万
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财政年份:2011
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负责人:Dianqing Wu
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依托单位:
Signaling Mechanisms for Leukocyte Migration Regulation
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批准号:8695455
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项目类别:
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资助金额:$48.2万
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财政年份:2011
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负责人:Dianqing Wu
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依托单位:
Signaling Mechanisms for Leukocyte Migration Regulation
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批准号:8504529
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项目类别:
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资助金额:$46.83万
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财政年份:2011
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负责人:Dianqing Wu
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依托单位:
Signaling Mechanisms for Leukocyte Migration Regulation
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批准号:8319373
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项目类别:
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资助金额:$49.04万
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财政年份:2011
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负责人:Dianqing Wu
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依托单位:
Chemoattactant signaling, macrophage functions and atherogenesis
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批准号:8150051
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项目类别:
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资助金额:$42.13万
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财政年份:2010
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负责人:Dianqing Wu
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依托单位:
Wnt signaling
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批准号:8019088
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项目类别:
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资助金额:$37.72万
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财政年份:2009
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负责人:Dianqing Wu
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依托单位:
Wnt signaling
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批准号:8212562
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项目类别:
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资助金额:$37.52万
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财政年份:2009
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负责人:Dianqing Wu
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依托单位:
Wnt signaling
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批准号:8445308
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项目类别:
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资助金额:$35.1万
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财政年份:2009
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负责人:Dianqing Wu
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依托单位:
Investigation of the role of AMP-activated protein kinase alpha2 (AMPKa2) in bone
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批准号:7685852
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项目类别:
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资助金额:$5.09万
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财政年份:2009
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负责人:Dianqing Wu
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依托单位: