Endothelium-derived Extracellular Vesicles, MicroRNAs and Pulmonary Hypertension
Endothelium-derived Extracellular Vesicles, MicroRNAs and Pulmonary Hypertension
批准号:
10009820
负责人:
Tianji Chen
金额:
$59.97万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-09-20 至 2022-08-31
关键词:
AffectAirAnimal ModelAreaBloodBlood CirculationBlood VesselsCellsCessation of lifeChronicDataDevelopmentDiseaseEndothelial CellsEndotheliumEngineeringFailureGene ExpressionGene ProteinsGoalsGrantHeartHumanHypoxiaIn VitroInjectionsKnowledgeLeadLungMass Spectrum AnalysisMicroRNAsMusPathogenesisPathway interactionsPatientsProteomicsPulmonary HypertensionPulmonary PathologyPulmonary artery structureRNARattusRegulationResearchResistanceRodent ModelRoleSeveritiesSideSmooth Muscle MyocytesStructure of parenchyma of lungTNF receptor-associated factor 3TestingTherapeutic AgentsTransfectionTransforming Growth Factor betaVascular Endothelial CellVascular Smooth MuscleVascular remodelingVentricularVesiclebasedesignextracellular vesiclesin vivoinnovationmiRNA expression profilingnovelnovel strategiesnovel therapeutic interventionpressurepreventtreatment strategyvascular smooth muscle cell proliferation
中文摘要
摘要
英文摘要
ABSTRACT
Our long term goals are to understand the mechanisms by which pulmonary vascular smooth muscle cell
(PASMC) proliferation is regulated in the context of vascular remodeling in pulmonary hypertension (PH). In the
lung, the pulmonary vascular endothelial cell (PVEC) regulates the function and proliferation of the underlying
smooth muscle cell (PASMC) by various bioactive agents that get to the PASMC via into the circulation,
myoendothelial junctions and/or extracellular vesicles (EV). The central hypothesis is that in hypoxia, PVEC-
derived EV contain microRNA that not only promote PASMC proliferation but also those that inhibit proliferation
and it is the imbalance between these two types of microRNAs that leads to disease. The objective of this grant
is to characterize the role of EV and their microRNA cargo in hypoxia, in modulating the progression of pulmonary
vascular remodeling and PH. Our specific aims are 1) To determine the role of PVEC-derived EV and the roles
of two of their miRNA cargo, miR-212-5p and miR-210-3p, in modulating vascular remodeling in hypoxia-induced
PH. 2) To determine the mechanisms by which miR-212-5p inhibits PASMC proliferation; specifically the roles
of TNF Receptor Associated Factor 3 (TRAF3) and the TGF- pathway and KLF4 in the inhibitory effect of miR-
212-5p on PASMC proliferation. In addition, novel targets of miR-212-5p and miR-210-3p will be identified using
iTRAQ mass spectrometry/proteomics analysis. 3) To provide proof of concept that engineered EV can be used
to treat severe PH. We will engineer EV to carry miR-212-5p and anti-miR-210-3p and determine if they can
ameliorate PH in two rodent models of PH. This contribution is significant since it will establish a critical role for
PVEC-derived EV and their microRNA cargo in the pathogenesis of PH; will delineate the role of miR-212-5p as
an important negative regulator of pulmonary vascular remodeling and PH and will test the possibility of utilizing
engineered EV for treatment of severe PH. The proposed research is innovative and knowledge derived from
the proposal should open new areas for further exploration and enable us to find new treatment strategies for
severe PH.
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国内基金
海外基金
湍流和化学交互作用对H2-Air-H2O微混燃烧中NO生成的影响研究
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批准号:51976048
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项目类别:面上项目
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资助金额:61.0万元
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批准年份:2019
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负责人:邱朋华
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依托单位: