Restoring LV Function Post-MI Using Fibrin-Gel Based Engineered Myocardium
Restoring LV Function Post-MI Using Fibrin-Gel Based Engineered Myocardium
批准号:
8037270
负责人:
Lauren D. Black III
金额:
$24.9万
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:
2010-05-24 至 2013-04-30
关键词:
AddressAnatomyAreaArterial Fatty StreakAwardBiologicalBiomedical EngineeringBiomimeticsBioreactorsCardiacCardiologyCardiovascular DiseasesCause of DeathCell TherapyCellsCommunicationCoronary arteryCouplingDevelopmentEngineeringEnvironmentEvaluationFibrinFundingGelGoalsHealthHeartHeart DiseasesHeart TransplantationHeart failureHumanIn VitroIncidenceInfarctionInnovative TherapyLeadLearningLeft Ventricular FunctionLeft ventricular structureMechanical StimulationMechanicsMentorsMethodsModelingMolecularMorphologyMuscle CellsMyocardialMyocardial InfarctionMyocardial tissueMyocardiumNatural regenerationOperative Surgical ProceduresPatientsPhasePhysiologicalPhysiologyPositioning AttributePropertyRattusResearchResearch InstituteResearch ProposalsTechniquesTimeTissue Culture TechniquesTissue EngineeringTissue GraftsTissuesUniversitiesWorkbasecareercomparative efficacydesignfunctional restorationheart functionimplantationimprovedin vivoinjuredinnovationpreventrepairedskills
中文摘要
心血管疾病可导致心肌梗死(Ml)和随后的心力衰竭。确实有
目前,许多治疗方法旨在预防或治疗心肌梗塞后的心力衰竭。只有心
移植替代梗死心肌以恢复心功能,但供体匮乏
心脏和心血管疾病的发病率持续上升。一种新的和创新的选择是使用
在体外制造的用于体内植入的“心脏贴片”。在独立阶段提出的研究
该奖项旨在解决与心脏功能和最终使用有关的两个关键问题
贴片:1)仿生培养环境对组织形态和功能的影响;2)贴片
体外仿生工程心肌等效物恢复左心功能的效果
心肌梗死后。这项工作的总体假设是,心肌在体外仿生培养中被工程化
条件比基于细胞治疗的修复方法更好地恢复心肌梗塞后的左心功能。这个
塔夫茨大学的环境使我能够回答这个假设,作为世界知名的
组织工程研究中心和分子心脏病研究所都位于附近。
这种环境将使我有机会充实我在组织方面已经相当丰富的背景。
与心脏解剖和生理学有关的力学和组织工程方法在健康和疾病和
心脏外科技术。在独立阶段继续我的职业规划包括
在细胞和组织培养技术以及生物反应器开发方面获得更多专业知识,同时学习新的
包括心脏外科技术和ML大鼠模型的生理学评估在内的技能。这个
该项目的最终目标是利用这些技能直接比较心肌组织的功效
以目前细胞疗法为基础的体外工程心脏修复方法在恢复左侧功能中的作用
心肌梗塞后的脑室。考虑到心脏病发病率的持续上升,这项研究尤其重要
疾病。这项研究的结果可能有助于阐明设计参数对创建
在体外进行功能心肌工程,从而使“心脏补片”的概念更接近现实
英文摘要
Cardiovascular disease can lead to myocardial infarction (Ml) and subsequent heart failure. There are
currently a number of therapies aimed at preventing or treating heart failure post-MI. Only heart
transplantation replaces infarcted myocardium to restore heart function, but there is a paucity of donor
hearts and the incidence of cardiovascular disease continues to rise. A new and innovative option is the use
of "heart patches" created in vitro for implantation in vivo. The research proposed in the independent phase
of this award aims to address 2 critical issues pertaining to the function and eventual use of such heart
patches: 1) the effect of a biomimetic culture environment on tissue morphology and function, and 2) the
efficacy of myocardial equivalents biomimetically-engineered in vitro in restoring left ventricular function
post-MI. The overall hypothesis of this work is that myocardium engineered in vitro in biomimetic culture
conditions restores post-MI left ventricular function better than cell therapy-based methods of repair. The
environment at the Tufts University uniquely positions me to address this hypothesis, as the world-renowned
Tissue Engineering Research Center and Molecular Cardiology Research Institute are both located nearby.
This environment will give me the opportunity to augment my already considerable background in tissue
mechanics and tissue engineering methods with cardiac anatomy and physiology in health and disease and
cardiac surgical techniques. The continuation of my career plan during the independent phase includes
gaining more expertise in cell and tissue culture techniques and bioreactor development, while learning new
skills in areas including cardiac surgical techniques and physiological evaluation in a rat model of Ml. The
ultimate goal of the project is to leverage these skills to directly compare the efficacy of myocardial tissue
engineered in vitro with current cell-therapy based methods of cardiac repair in restoring function to the left
ventricle post-MI. This research is especially critical considering the continuing rise in incidence of heart
disease. The results of this research may help elucidate design parameters that are critical to the creation of
functional myocardium engineered in vitro and thus advance the concept of the "heart patch" closer to reality
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会议论文
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批准号:10705333
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资助金额:$38.47万
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财政年份:2022
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负责人:Lauren D. Black III
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依托单位:
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The role of the extracellular biophysical and biomechanical milieu in CHDs
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资助金额:$17.39万
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批准号:8535815
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资助金额:$37.39万
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财政年份:2012
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负责人:Lauren D. Black III
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依托单位:
Restoring LV Function Post-MI Using Fibrin-Gel Based Engineered Myocardium
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批准号:8270013
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项目类别:
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资助金额:$24.9万
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财政年份:2010
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负责人:Lauren D. Black III
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依托单位:
Restoring LV Function Post-MI Using Fibrin-Gel Based Engineered Myocardium
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批准号:8076797
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项目类别:
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资助金额:$24.9万
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财政年份:2010
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负责人:Lauren D. Black III
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依托单位:
Restoring LV Function Post-MI Using Fibrin-Gel Based Engineered Myocardium
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批准号:7659862
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资助金额:$7.89万
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财政年份:2009
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负责人:Lauren D. Black III
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依托单位:
Engineered Cell Alignment for Improved Beating in a Fibrin-Based Heart Patch
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批准号:7274650
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项目类别:
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资助金额:$4.83万
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财政年份:2007
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负责人:Lauren D. Black III
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依托单位:
Engineered Cell Alignment for Improved Beating in a Fibrin-Based Heart Patch
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批准号:7429680
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财政年份:2007
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依托单位:
海外基金