Length-dependent activation in human myocardium
人类心肌的长度依赖性激活
基本信息
- 批准号:10468226
- 负责人:
- 金额:$ 67.56万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2020
- 资助国家:美国
- 起止时间:2020-09-15 至 2024-07-31
- 项目状态:已结题
- 来源:
- 关键词:AmericanBiochemicalBiological AssayBiophysicsCalciumCardiacCardiomyopathiesCardiovascular systemComputer ModelsDataData SetDependenceDevelopmentDiseaseElectrophoresisGeneticGenomicsHeadHeart TransplantationHeart failureHistologicHistologyHumanImpairmentInfarctionKentuckyLengthLevosimendanMusMuscle CellsMuscle ContractionMutationMyocardialMyocardial IschemiaMyocardiumMyosin ATPaseOrgan DonorPatientsPenetrancePeptidesPharmacologic SubstancePhenotypePhysiciansPhysiologic pulsePilot ProjectsPreparationPropertyRegulationResearchResearch PersonnelResourcesSamplingSarcomeresScientistSpecimenStretchingStructureSturnus vulgarisTechniquesTestingThick FilamentTransplantationUniversitiesbasebiobankbiophysical techniquesdesignexperimental studygel electrophoresisgenomic datahuman dataorgan transplant recipientpredictive modelingpreservationskills
项目摘要
ABSTRACT
This translational project uses human biospecimens procured from organ donors and patients undergoing
cardiac transplant to advance understanding of a cellular-level mechanism that underpins the Frank-Starling
relationship. Specifically, the project focuses on length-dependent activation, defined as the increased maximum
force and Ca2+ sensitivity of contraction induced by myocardial stretch. The mechanisms that underlie length-
dependent activation remain unclear, but may involve thick-filament regulation and transitions between the newly
discovered OFF and ON states of myosin.
Co-PI Campbell has spent a decade building a biobank that now contains >10,000 myocardial specimens from
>360 patients. Pilot experiments performed by Co-PI Tanner with these samples show that length-dependent
changes in Ca2+ sensitivity are eliminated in myocardium from patients who have non-ischemic heart failure, but
preserved in myocardium from organ donors and patients who have ischemic heart failure. New computer
modeling predicts that these functional effects reflect destabilization of the myosin OFF state in patients who
have non-ischemic heart failure. This hypothesis is supported by additional experiments that used fluorescent
polarization techniques to assess OFF/ON dynamics in the thick filaments of human myocardium. Further pilot
studies tested the effects of peptides targeted to the thick filament. Peptides that stabilize the OFF state reduced
the Ca2+ sensitivity of contraction at long sarcomere length while destabilizing peptides enhanced Ca2+ sensitivity
at short length. The length-dependence of these effects was predicted by our computer modeling.
The project builds on these data from human biospecimens and integrates the skills and resources of five
cardiovascular researchers, a statistician, and a physician-scientist who specializes in advanced heart failure.
The Aims explore the global hypothesis that length-dependent activation is reduced in patients who have non-
ischemic heart failure because their cardiac thick filaments are biased towards the ON state.
Aim 1: Test the hypothesis that length-dependent changes in Ca2+ sensitivity are reduced in myocardium from
patients who have non-ischemic heart failure.
Aim 2: Test the hypothesis that the OFF state of the thick filament is destabilized in myocardium from patients
who have non-ischemic heart failure.
Aim 3: Target OFF/ON transitions to manipulate the Ca2+ sensitivity of human myocardium.
摘要
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Kenneth S Campbell其他文献
Unfolded Von Willebrand Factor Interacts with Protein S and Limits Its Anticoagulant Activity
- DOI:
10.1182/blood-2022-162612 - 发表时间:
2022-11-15 - 期刊:
- 影响因子:
- 作者:
Martha MS Sim;Hammodah Alfar;Melissa Hollifield;Dominic W. Chung;Xiaoyun Fu;Meenakshi Banerjee;Chi Peng;Xian Li;Alice Thornton;James Z Porterfield;Jamie Sturgill;Gail A Sievert;Marietta Barton-Baxter;Kenneth S Campbell;Jerold G Woodward;José A. López;Sidney W Whiteheart;Beth A Garvy;Jeremy P Wood - 通讯作者:
Jeremy P Wood
Kenneth S Campbell的其他文献
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{{ truncateString('Kenneth S Campbell', 18)}}的其他基金
Carol Act Supplement to Data-driven optimization of therapy for heart failure
卡罗尔法案对数据驱动的心力衰竭治疗优化的补充
- 批准号:
10851206 - 财政年份:2022
- 资助金额:
$ 67.56万 - 项目类别:
Data-driven optimization of therapy for heart failure
数据驱动的心力衰竭治疗优化
- 批准号:
10467277 - 财政年份:2022
- 资助金额:
$ 67.56万 - 项目类别:
Data-driven optimization of therapy for heart failure
数据驱动的心力衰竭治疗优化
- 批准号:
10615143 - 财政年份:2022
- 资助金额:
$ 67.56万 - 项目类别:
Dual filament control of myocardial power and hemodynamics
心肌功率和血流动力学的双丝控制
- 批准号:
10245290 - 财政年份:2020
- 资助金额:
$ 67.56万 - 项目类别:
Dual filament control of myocardial power and hemodynamics
心肌功率和血流动力学的双丝控制
- 批准号:
10472655 - 财政年份:2020
- 资助金额:
$ 67.56万 - 项目类别:
Dual filament control of myocardial power and hemodynamics
心肌功率和血流动力学的双丝控制
- 批准号:
10672422 - 财政年份:2020
- 资助金额:
$ 67.56万 - 项目类别:
Length-dependent activation in human myocardium
人类心肌的长度依赖性激活
- 批准号:
10678926 - 财政年份:2020
- 资助金额:
$ 67.56万 - 项目类别:
Length-dependent activation in human myocardium
人类心肌的长度依赖性激活
- 批准号:
10259881 - 财政年份:2020
- 资助金额:
$ 67.56万 - 项目类别:
Multiscale modeling of inherited cardiomyopathies and therapeutic interventions
遗传性心肌病的多尺度建模和治疗干预
- 批准号:
10223922 - 财政年份:2017
- 资助金额:
$ 67.56万 - 项目类别:
Multiscale modeling of inherited cardiomyopathies and therapeutic interventions
遗传性心肌病的多尺度建模和治疗干预
- 批准号:
9980457 - 财政年份:2017
- 资助金额:
$ 67.56万 - 项目类别:
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