The role of the BMP type II receptor in vascular function
The role of the BMP type II receptor in vascular function
批准号:
7589690
负责人:
PAUL B YU
金额:
$13.43万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-04-01 至 2011-03-31
关键词:
AblationAbnormal CellAddressAdultAdvisory CommitteesAffectAnimal ModelAnimalsApoptosisBMPR2 geneBiologyBlood CirculationBlood VesselsBone Morphogenetic ProteinsCardiacCardiologyCell ProliferationCell physiologyCellsCellular biologyDevelopmentDevelopment PlansDiseaseEmbryoEnvironmentFacultyFamilyFellowshipFibrosisFoundationsGene ExpressionGene MutationGeneral HospitalsGenetic TranscriptionGrowth FactorHealthHistologyIn SituIn VitroIntegrinsInvestigationLeadLesionLigandsLungMassachusettsMediatingMentorshipMolecularMolecular GeneticsMusMutationMyofibroblastOrganogenesisPathologicPathway interactionsPatientsPatternPhysiciansPhysiologicalPhysiologyPrincipal InvestigatorProliferatingProstatePulmonary HypertensionPulmonary artery structureReportingResearchResearch PersonnelRight Ventricular FunctionRoleScientistSignal PathwaySignal TransductionSmooth MuscleSmooth Muscle MyocytesSolidStructureSystemTechnical ExpertiseTestingTimeTissuesTrainingTransforming Growth FactorsTumor Suppressor ProteinsVascular DiseasesWorkbone morphogenetic protein receptor type IIbone morphogenetic protein receptorscareercareer developmentexperiencegastrulationhemodynamicsimprovedin vivoinsightintimal medial thickeningkidney cellloss of function mutationmeetingsmembermigrationnew growthprimary pulmonary hypertensionprogramsreceptorresearch studyskills
中文摘要
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英文摘要
The proposed research examines the function of bone morphogenetic protein (BMP) signaling in the
vasculature. Previous work in the field has demonstrated the impact of BMP signals upon the function of
vascular endothelial and smooth muscle cells, indicating that BMP signals are important regulators of vessel
brmation and remodeling. Loss-of-function mutations in the principal receptor for BMP signals, the BMP
type II receptor (BMPR2) are implicated in the vasculopathic disease primary pulmonary hypertension,
urther supporting an essential role in vascular function. However, the mechanisms by which BMP signals
modify the function of vascular tissues are incompletely defined. Use of the Cre-lox system and genetically
modified mice has permitted tissue-specific disruption of the BMPR2 gene in vivo and in vitro. The impact of
BMPR2 signaling upon vascular cell functions and transcriptional activity will be investigated, as well as the
potential mechanisms of effect. Cell physiology will be correlated with the impact of disrupting BMPR2 in
vivo, using the endpoints of pulmonary vascular hemodynamic function, structure and development. These
studies will help define the role of BMPR2 and BMP signaling in normal and pathologic vascular function and
may provide an animal model of pulmonary hypertension. Completion of the research program and the
acquisition of the required skills and experience will provide a solid foundation for the development of a
career as a physician-scientist specializing in cardiac and pulmonary vascular biology.
The principal investigator is transitioning from fellowship training to faculty in the Division of Cardiology at
Massachusetts General Hospital and proposes to expand upon his scientific skills in molecular genetics, cell
biology, and animal physiology to facilitate the transition to independence as an investigator skilled in
integrating molecular and physiologic aspects of disease. The career development plan includes scientific
and career mentorship from an advisory committee of accomplished scientists; participation in relevant
seminars, courses, and national meetings; and the provision of protected research time. The proposal will
take advantage of extensive local technical expertise and the highly collaborative environment present at
Massachusetts General Hospital.
Health Relevance: Bone morphogenetic proteins are used by cells to coordinate growth of new tissues and
maintain existing tissues, and are especially important in developing and maintaining normal blood vessels.
This study examines in mice how a receptor for bone morphogenetic proteins (BMPR2) coordinates the
function of blood vessel cells, and how abnormal function of BMPR2 may lead to disorders of the circulation.
期刊论文(0)
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会议论文
Context-specific angiogenic signaling in the pulmonary vasculature
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批准号:10280040
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项目类别:
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资助金额:$62.56万
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财政年份:2021
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依托单位:
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Molecular and cellular mechanisms of heterotopic ossification
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批准号:10238889
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资助金额:$7.65万
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财政年份:2010
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依托单位:
Molecular and cellular mechanisms of heterotopic ossification
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批准号:8538700
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项目类别:
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资助金额:$5.98万
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财政年份:2010
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负责人:PAUL B YU
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依托单位:
Molecular and cellular mechanisms of heterotopic ossification
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批准号:8116468
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项目类别:
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资助金额:$38.53万
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财政年份:2010
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负责人:PAUL B YU
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依托单位:
Molecular and cellular mechanisms of heterotopic ossification
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批准号:7993157
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项目类别:
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资助金额:$39.09万
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财政年份:2010
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负责人:PAUL B YU
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依托单位:
Molecular and cellular mechanisms of heterotopic ossification
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批准号:10005031
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项目类别:
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资助金额:$66.03万
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依托单位:
Molecular and cellular mechanisms of heterotopic ossification
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批准号:8325423
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资助金额:$38.56万
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Molecular and cellular mechanisms of heterotopic ossification
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批准号:10757487
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资助金额:$29.24万
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Molecular and cellular mechanisms of heterotopic ossification
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批准号:10685932
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资助金额:$36.74万
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依托单位:
Molecular and cellular mechanisms of heterotopic ossification
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批准号:9753912
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项目类别:
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资助金额:$39.38万
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财政年份:2010
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负责人:PAUL B YU
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依托单位:
Molecular and cellular mechanisms of heterotopic ossification
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批准号:8500210
-
项目类别:
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资助金额:$43.46万
-
财政年份:2010
-
负责人:PAUL B YU
-
依托单位:
The role of the BMP type II receptor in vascular function
-
批准号:7211349
-
项目类别:
-
资助金额:$13.43万
-
财政年份:2006
-
负责人:PAUL B YU
-
依托单位:
The role of the BMP type II receptor in vascular function
-
批准号:7790705
-
项目类别:
-
资助金额:$13.43万
-
财政年份:2006
-
负责人:PAUL B YU
-
依托单位:
The role of the BMP type II receptor in vascular function
-
批准号:7077169
-
项目类别:
-
资助金额:$13.43万
-
财政年份:2006
-
负责人:PAUL B YU
-
依托单位:
The role of the BMP type II receptor in vascular function
-
批准号:7388825
-
项目类别:
-
资助金额:$13.43万
-
财政年份:2006
-
负责人:PAUL B YU
-
依托单位:
海外基金