The paradoxical role of CDKN2B in blood vessel sprouting and maturation
The paradoxical role of CDKN2B in blood vessel sprouting and maturation
批准号:
8968859
负责人:
Nicholas James Leeper
金额:
$46.49万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-11-15 至 2019-10-31
关键词:
9p21AccountingAnimalsApoptosisArterial Fatty StreakAtherosclerosisBiological AssayBiologyBlood VesselsCDKN2B geneCandidate Disease GeneCardiovascular DiseasesCardiovascular systemCause of DeathCellsChromosomesChromosomes, Human, Pair 9Coculture TechniquesCohort StudiesCollaborationsCoronary ArteriosclerosisDefectDevelopmentDiseaseDominant-Negative MutationEndothelial CellsEnrollmentEventFigs - dietaryGenesGeneticGenetic PolymorphismGenetic RiskGenetic VariationGenetic studyHealthHeartHemorrhageHindlimbHumanHyperlipidemiaHypertensionHypoxiaIn VitroIndividualInheritedIntramuscularIschemiaLeadLigationLimb structureLinkMapsMediatingMissionMolecularMolecular GeneticsMusMyocardial InfarctionOperative Surgical ProceduresPathologicPathway interactionsPatientsPericytesPeripheral arterial diseasePhagocytosisPhenotypePhosphorylationPhysiologyProcessPublishingQuantitative Trait LociResearch PersonnelRiskRisk FactorsRoleRuptureSamplingScientistSecondary toSignal TransductionSmokingSmooth Muscle MyocytesSourceTP53 geneTissue SampleTransfectionTransgenic OrganismsTranslatingTubeTumor Suppressor ProteinsUnited StatesUnited States National Institutes of HealthVariantVascular DiseasesVascular Endothelial Growth FactorsWestern WorldWorkangiogenesisatherogenesisbasecardiovascular risk factorcell behaviorcell typedisorder riskfemoral arterygenome wide association studyhuman tissuein vivoinsightknockout animallifetime riskmacrophagemanmatrigelmouse modelneovascularizationnovelnovel therapeuticspleiotropismresponserisk variant
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Genome-wide association studies (GWAS) have recently identified a region of chromosome 9p21 as the most important source of heritable cardiovascular risk. This locus is independent of traditional risk factors such as smoking, hypertension and hyperlipidemia, suggesting it potentiates disease via a novel mechanism. The most predictive 9p21 variants account for more than 20% of an individual's lifetime risk for coronary artery disease. Despite being implicated in the leading cause of death in the Western world, the mechanism(s) by which these polymorphisms lead to vascular disease remain unclear. In this proposal, the investigators seek to elucidate the relationship between a leading candidate gene at the 9p21 risk locus, CDKN2B, and vascular disease. Specifically, they will query the role of this gene in angiogenesis, and the concept that CDKN2B may regulate disease via a paradoxical and antagonistic effect on blood vessel sprouting, and blood vessel maturation. This proposal will bring together recognized experts from several fields, deeply phenotyped human tissue samples and unique mouse models with the objective of fully describing the vascular biology of CDKN2B. This application includes three specific aims which will: 1) Map the molecular mechanism by which CDKN2B regulates blood vessel stabilization; 2) Employ novel cell-specific Cdkn2b knockout animals to specifically determine which cell type regulates the pathologic response to ischemia, and whether the process is reversible; and 3) Determine whether the angiogenic defect also promotes atherosclerotic plaque vulnerability and myocardial infarction in human carriers of the 9p21 risk allele. The objective of these studies is to 'reverse translate' the biology of the 9p21 locus and contribute to the field of cardiovascular genetics in the post-GWAS era. Discoveries made in the course of this proposal are intended to support the stated mission of the National Institutes of Health and provide contributions that will
lead to the development of new translational therapies for patients with cardiovascular disease.
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