MicroRNA in Functional Regulation of Endothelial Cells in Response to Flow
MicroRNA in Functional Regulation of Endothelial Cells in Response to Flow
批准号:
8208978
负责人:
SHU CHIEN
金额:
$78.43万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-01-01 至 2014-11-30
关键词:
AnimalsAntiatherogenicApolipoprotein EApoptosisAreaArterial Fatty StreakBioinformaticsBiologicalBiological AvailabilityBiologyBiomechanicsBlood VesselsBlood flowCardiovascular DiseasesCardiovascular systemCell LineCell physiologyComplexComputer SimulationDataData AnalysesDevelopmentDiagnosisEndothelial CellsEndotheliumEventFunctional RNAGene ExpressionGene Expression ProfileGenesGenomicsHistocompatibility TestingHuman GenomeImmunoprecipitationIn VitroInflammationInflammatoryLesionLeukocyte ChemotaxisLiquid substanceLiteratureMaintenanceMapsMechanicsMessenger RNAMicroRNAsModelingModificationMolecularMolecular ProfilingMusPathway interactionsPatternPhenotypePlayProteinsRegulationResearchResearch Project GrantsRoleSystemSystems BiologyTechnologyTestingThoracic aortaTissue-Specific Gene ExpressionTranslational RepressionTreesVascular Endothelial CellWorkaortic archbasecDNA Arrayscrosslinkfunctional genomicsgene functiongenome-widein vivoinnovationinsightloss of functionmRNA Stabilitymouse modelmultidisciplinarynovel strategiesprotein expressionresearch studyresponseshear stress
中文摘要
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英文摘要
Project Summary:
MicroRNAs (miRs) are small non-coding RNAs that play crucial roles in regulating mRNA stability and
translational repression. There is increasing evidence that miRs can modulate gene expression in the
cardiovascular system. Endothelial cells (ECs) lining the vascular lumen are sensitive to mechanical factors
such as fluid shear stress. During the past two decades, this research team has worked on the mechanisms of
mechanotransduction in ECs and the consequent gene expression. The results from them and others indicate
that steady and pulsatile shear stresses (PS) with a net forward direction are anti-atherogenic by inducing
genes involved in anti-proliferation and anti-inflammation. In contrast, oscillatory shear stress (OS) without a
significant forward direction is pro-atherogenic by activating pro-proiferative and pro-inflammatory genes.
Based on new evidence in the literature and our recent findings that miRs play an important role in regulating
EC genes, we hypothesize that anti-atherogenic (PS) and pro-atherogenic (OS) flow patterns induce distinct
patterns of miRs, and hence the differential gene expressions and functional consequences. We will use in
vitro, in vivo, and in silico approaches to develop an integrated system to elucidate the roles of miRs in
regulating EC functions in response to different flow patterns. This multi-P.I. research project, by combining
experimental data obtained from cultured ECs and mouse models with molecular, genomics and systems
approaches, will elucidate the mechanisms of functional regulation by miRs in ECs under flows. In order to test
our hypothesis, we propose the following five specific aims: (1) To establish miR expression profiles in cultured
ECs in response to PS vs. OS. (2) To determine the target mRNAs of miRs in response to PS vs. OS. (3) To
decipher the functional gene expression profiles regulated by miRs under PS vs. OS. (4) To elucidate the
functional consequences of miR regulation under PS vs. OS. (5) To verify the role of miRs in functional
regulation of vascular ECs exposed to different flow patterns in vivo. In this proposal the role of miR in
regulating vascular functions will be studied under different flow patterns with a combination of experimental
and computational approaches to perform multi-scale analyses from miRs/mRNAs to cellular functions. This
innovative, multidisciplinary project includes (a) comprehensive genome-wide approaches to establish the miR
profiles in ECs, (b) CLIP-seq approaches to elucidate the interactions between miRs and target mRNAs, (c)
systems biology approaches to map the functional gene expression and biological consequence regulated by
miRs, and (d) in vivo approaches in lesion-induction mice to validate the roles of miRs under different flow
patterns established in vitro. The results will enhance the mechanistic insights of the roles of mechano-
regulation and functional genomics at the systems biology level and may contribute to the development of
novel approaches for the diagnosis and treatment of cardiovascular diseases.
期刊论文(0)
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科研奖励(0)
会议论文
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财政年份:2015
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批准号:8615815
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财政年份:2013
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财政年份:2013
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资助金额:$55.47万
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财政年份:2013
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资助金额:$79.0万
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财政年份:2013
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依托单位:
Systems Biology Analyses for Hemodynamic Regulation of Vascular Homeostasis
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批准号:8332732
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资助金额:$109.07万
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财政年份:2012
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批准号:9111932
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资助金额:$96.63万
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财政年份:2012
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依托单位:
Systems Biology Analyses for Hemodynamic Regulation of Vascular Homeostasis
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批准号:10448495
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资助金额:$103.74万
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财政年份:2012
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负责人:SHU CHIEN
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依托单位:
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财政年份:2012
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财政年份:2012
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负责人:SHU CHIEN
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依托单位:
Systems Biology Analyses for Hemodynamic Regulation of Vascular Homeostasis
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批准号:9403707
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项目类别:
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资助金额:$105.76万
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财政年份:2012
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负责人:SHU CHIEN
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依托单位:
Systems Biology Analyses for Hemodynamic Regulation of Vascular Homeostasis
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批准号:8536356
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项目类别:
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资助金额:$101.78万
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财政年份:2012
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负责人:SHU CHIEN
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依托单位:
Systems Biology Analyses for Hemodynamic Regulation of Vascular Homeostasis
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批准号:8722012
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项目类别:
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资助金额:$103.51万
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财政年份:2012
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负责人:SHU CHIEN
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依托单位:
Systems Biology Analyses for Hemodynamic Regulation of Vascular Homeostasis
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批准号:10318053
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资助金额:$106.25万
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财政年份:2012
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负责人:SHU CHIEN
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依托单位:
MicroRNA in Functional Regulation of Endothelial Cells in Response to Flow
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批准号:8266924
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项目类别:
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资助金额:$4.14万
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财政年份:2011
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负责人:SHU CHIEN
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依托单位:
MicroRNA in Functional Regulation of Endothelial Cells in Response to Flow
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批准号:8034113
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财政年份:2011
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负责人:SHU CHIEN
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Nucleolin Regulation of miRome by Shear Stress
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资助金额:$58.38万
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负责人:SHU CHIEN
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依托单位:
海外基金