MicroRNAs in brown fat development and metabolism
MicroRNAs in brown fat development and metabolism
批准号:
9256460
负责人:
Yong-Xu Wang
金额:
$36.43万
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:
2014-07-21 至 2019-03-31
关键词:
3&apos Untranslated RegionsAddressAdipocytesAdipose tissueAdultAffectAnimalsBase PairingBrown FatCell Culture TechniquesCell Differentiation processCell physiologyCellsCharacteristicsCyclic GMPCyclic NucleotidesDataDevelopmentDevelopmental ProcessDietDown-RegulationEnergy MetabolismEvolutionExonsFatty acid glycerol estersGene ExpressionGenesGenetic Predisposition to DiseaseGenetic TranscriptionGoalsGuanosine MonophosphateHumanIn VitroInsulin ResistanceIntronsLeadMediatingMessenger RNAMetabolicMetabolic DiseasesMetabolismMicroRNAsModelingMolecularMusNatureNon-Insulin-Dependent Diabetes MellitusObesityPPAR PathwayPathway interactionsPeriodicityPhosphodiesterase InhibitorsPhysiologicalPhysiologyPlayProtein KinaseProteinsRegulationResistanceRoleSeedsSignal PathwaySignal TransductionSignaling MoleculeSiteSmall RNASurveysTherapeuticTissuesTransgenesTransgenic MiceTransgenic OrganismsTranslational RepressionUntranslated RNAenergy balanceexperimental studyimprovedin vivoinhibitor/antagonistinsulin sensitivityinterestknock-downlipid biosynthesismembermetabolic phenotypenovel therapeuticsoverexpressionphosphoric diester hydrolasepreventprotein activationpublic health relevanceselective expressiontherapeutic targettranscriptome sequencing
中文摘要
描述(由申请人提供):我们的长期目标是了解控制棕色脂肪发育和功能的分子途径。与白色脂肪相比,棕色脂肪是一种专门用于能量消耗的组织。它存在于成人中,其活性是
英文摘要
DESCRIPTION (provided by applicant): Our long-range goal is to understand molecular pathways that govern brown fat development and function. In contrast to white fat, brown fat is a tissue that is specialized in energy expenditure. It is present in adult humans and its activity is
inversely associated with human obesity. Thus, brown fat is potentially an attractive therapeutic target tissue for obesity and metabolic diseases. We are interested in how brown fat development and function is regulated by miRNAs, a class of small RNAs that do not encode protein yet control many developmental and cellular processes. We have identified a set of miRNAs that are selectively expressed in the brown fat. We found that, one of them, when expressed in the brown fat, remarkably expands the brown fat depots of mice, and as a result, the animals have less white fat mass and are resistant to diet-induced obesity. Our hypothesis is that this miRNA promotes brown fat cell differentiation by activating a cGMP- dependent signaling pathway. In the first aim, we will analyze in detail whether the expanded brown fat depots are true brown fat and are functional. We will determine whether the expanded brown fat improves metabolic parameters and enhances insulin sensitivity. We will determine whether the expanded brown fat prevents genetically predisposed obesity. In the second aim, we will perform cell culture studies to further validate that this miRNA promotes brown cell differentiation. We will examine whether the miRNA represses the expression of a negative regulator in the cGMP-dependent signaling pathway. In the third aim, we will determine whether the miRNA activates the cGMP-dependent signaling pathway. Our studies will likely provide useful information on whether mimics of this miRNA have therapeutic potentials for obesity and metabolic diseases.
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会议论文
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海外基金