Perfusable and beating engineered myocardium from human progenitor cells based on
Perfusable and beating engineered myocardium from human progenitor cells based on
批准号:
8138261
负责人:
ROBERT T TRANQUILLO
金额:
$71.56万
依托单位:
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:
2011-09-05 至 2015-05-31
关键词:
AffectAutologousBiopolymersBioreactorsBloodCardiacCardiac MyocytesCellsCellular StructuresCellularityCharacteristicsCollagenCongestive Heart FailureContractsDataDepositionDevelopmentDyesEndothelial CellsEngineeringExtracellular MatrixFiberFibrinFibroblastsGelGenerationsGeneric DrugsGoalsHeartHeart failureHumanHypertrophyImplantIn VitroInfarctionKnowledgeMeasuresMechanicsMetabolicMethodsModelingMonitorMyocardial InfarctionMyocardiumNeonatalNude RatsOxygenPatientsPerfusionPericytesPhenotypePropertyRattusResearchScreening procedureSourceStem cellsStretchingSystemTechnologyThickTimeTissue EngineeringTissuesTracerTubeUmbilical veinVenousabstractingbasecell assemblycell typedesignfunctional outcomesimprovedinduced pluripotent stem cellinterstitialpreventreconstitutionresearch studyself assemblysuccesstissue culture
中文摘要
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英文摘要
DESCRIPTION (provided by applicant):
A critical need in tissue engineering is a means to create the equivalent of a microvasculature within relatively thick and/or metabolic engineered tissues, such as engineered myocardium. This proposal combines the use of stem cells from convenient autologous sources and the technology of guided cell assembly via cell entrapment in and subsequent remodeling of fibrin gel into aligned tissue in order to create a perfusable and beating engineered myocardium. Perfusable tissue constructs will be fabricated from blood outgrowth endothelial cells and pericytes. Beating tissue constructs will be fabricated from induced pluripotent stem cell (iPS)-derived cardiomyocytes. Perfusable and beating engineered myocardium will then be fabricated by co-entrapment of the three cell types using the same guided cell assembly methods, which are based on mechanically-constrained cell contraction and alignment of fibrin gel. These tissue constructs will be extensively characterized in vitro and then assessed in an infarcted rat heart model for improved functional outcomes. The results from this research will be both enabling technology for many engineered tissues - a means to create a functional microvasculature - and the basis for a functional heart patch that can treat myocardial infarcts and potentially prevent onset of congestive heart failure. (End of Abstract)
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海外基金