Improving fibrin-based bioartificial arteries by prolonging ERK activation
Improving fibrin-based bioartificial arteries by prolonging ERK activation
批准号:
8597625
负责人:
JUSTIN Sol WEINBAUM
金额:
$1.2万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-12-10 至 2013-02-28
关键词:
AmericanAmerican Heart AssociationArteriesAutologousBalloon AngioplastyBehaviorBiochemicalBiologicalBiological AssayBiomechanicsBioreactorsBlood PressureBypassCellsCellularityChemicalsCollagenCollagen Type ICoronary ArteriosclerosisCoronary heart diseaseDermalDevelopmentDiseaseEngraftmentEventFeedbackFellowshipFibrinFibroblastsGelGenetic TranscriptionGoalsHarvestHealthcareImmuneIn VitroIncubatedInfectionLeadLuciferasesMAPK14 geneMechanical StimulationMechanicsMinnesotaMitogen-Activated Protein KinasesMonitorMorbidity - disease rateOutcomePathway interactionsPatientsPhosphoric Monoester HydrolasesPhysiologic pulsePhysiologicalPolymersPolytetrafluoroethyleneProcessProductionPropertyQuality of lifeReporterReportingResearchRiskSamplingSaphenous VeinSignal PathwaySignal TransductionStentsStimulusSystemTensile StrengthTestingThrombosisTimeTissue EngineeringTissuesTrainingTransplantationTubular formationTunica MediaUniversitiesVascular GraftWorkWound Infectionbasecare burdenconditioninghemodynamicsimplantationimprovedinhibitor/antagonistinternal thoracic arteryneonatal humanpressurepreventpublic health relevanceresearch and developmentresponserestenosistype I collagen alpha 1
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英文摘要
DESCRIPTION (provided by applicant): Nationally, coronary artery disease is a tremendous health care burden. Current therapies for coronary artery disease suffer from multiple risks to the patient including restenosis, thrombosis, infection, and other graft disease. A completely biological bioartificial artery graft would circumvent these issues and improve the outcome for sufferers of coronary artery disease. Fibrin-based tissue engineering has already shown significant progress but as yet has not produced a bioartificial artery with sufficient mechanical strength for implantation without risk. A new strategy is needed to exploit signaling pathways for cellular stimulation. The hypothesis for the proposed work is that: Prolonged ERK signaling during in vitro culture will improve the mechanical strength of fibrin-based bioartificial arteries, via stimulation of type I collagen transcription and increased collagen content. By manipulating extracellular signal-regulated kinase (ERK) signaling by the cells seeded in tubular fibrin- based constructs, this project will improve the collagen content of bioartificial arteries and ultimately their mechanical strength. The specific aims of the proposed work are as follows: #1. Establish that ERK activity is necessary for the production of mechanically strong bioartificial arteries. #2. Promote prolonged ERK activation in bioartificial arteries by inhibiting negative feedback pathways. #3. Promote prolonged ERK activation in bioartificial arteries by mechanical stimulation. The primary readouts for the response to ERK signal manipulation will be type I collagen transcription, using a luciferase reporter, collagen content, using a biochemical assay, and mechanical strength, using mechanical testing systems. Significant training in tissue engineering and biomechanics from experts at the University of Minnesota will be a key goal for this fellowship. It is expected that this project will produce bioartificial arteries that can withstand physiological blood pressure.
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Improving fibrin-based bioartificial arteries by prolonging ERK activation
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批准号:8207809
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项目类别:
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资助金额:$5.57万
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财政年份:2010
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负责人:JUSTIN Sol WEINBAUM
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依托单位:
Improving fibrin-based bioartificial arteries by prolonging ERK activation
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批准号:8058406
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项目类别:
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资助金额:$5.58万
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财政年份:2010
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负责人:JUSTIN Sol WEINBAUM
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依托单位:
海外基金