Role of Progranulin in Mediating the Anti-Inflammatory Property of High-Density L
Role of Progranulin in Mediating the Anti-Inflammatory Property of High-Density L
批准号:
8706956
负责人:
Andrew D. Nguyen
金额:
$0.62万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-08-16 至 2014-08-31
关键词:
AgeAnti-Inflammatory AgentsAnti-inflammatoryApolipoprotein A-IApolipoprotein EAtherosclerosisBindingBloodCardiovascular DiseasesCell AdhesionCell Adhesion MoleculesCollagen ArthritisDiseaseEndothelial CellsEpidemiologic StudiesFrontotemporal DementiaGenesGleanGrowth FactorHigh Density Lipoprotein CholesterolHigh Density LipoproteinsHumanImmunoprecipitationIn VitroIncidenceIndividualInflammationInflammatoryIntercellular adhesion molecule 1KnowledgeLinkLipoproteinsMass Spectrum AnalysisMediatingModelingMolecularMusMutateMutationPGRN genePlasmaPlayPredispositionPreventionProgranulinPropertyProtein BindingProteinsRecombinantsReportingRoleSignal TransductionTNF geneTestingTherapeuticTissuesTumor Necrosis Factor ReceptorVascular Cell Adhesion Molecule-1basedensityin vivoinsightmacrophagemouse modelprotective effectreverse cholesterol transport
中文摘要
描述(由申请人提供):高密度脂蛋白(HDL)是血浆中最小、密度最大的脂蛋白。过去四十年的流行病学研究一致发现,HDL水平与心血管疾病的发病率呈负相关。HDL的保护作用主要归因于其在胆固醇逆向转运中的作用或其抗炎性质。1995年,基于HDL阻断TNF-α诱导的内皮细胞中细胞粘附分子VCAM-1和ICAM-1表达的能力,描述了抗炎特性。尽管许多研究已经证实了这一发现,但这种抗炎特性的机制仍然未知。我建议把重点放在一个新的候选人介导高密度脂蛋白的抗炎性质。颗粒蛋白原是一种分泌的生长因子,在许多组织中表达并在血液中循环。在家族性额颞叶痴呆的某些病例中,颗粒蛋白前体基因GRN发生突变。据报道,颗粒蛋白前体与HDL相关。有趣的是,最近的研究表明,颗粒蛋白前体与TNF受体结合,从而建立了颗粒蛋白前体与炎症之间的联系。具体地,目前的模型证实颗粒蛋白前体通过与TNF-α竞争结合TNF受体来拮抗TNF信号传导。此外,缺乏颗粒蛋白前体的小鼠对胶原诱导的关节炎的易感性增强,说明了涉及炎症的功能后果。这提出了一个有趣的假设,即颗粒蛋白前体显著有助于HDL的抗炎特性。这些研究的完成有望为HDL抗炎特性的分子基础提供重要的见解。从这些研究中收集的知识可能对预防和治疗心血管疾病具有治疗意义。此外,它与GRN基因突变的个体直接相关,GRN基因在某些额颞叶痴呆症病例中发生突变。
英文摘要
DESCRIPTION (provided by applicant): High-density lipoprotein (HDL) is the smallest, most dense lipoprotein in plasma. Epidemiological studies from the past four decades have consistently found that HDL levels are inversely correlated with the incidence of cardiovascular disease. The protective effect of HDL is largely attributed to either its role in reverse cholesterl transport or its anti-inflammatory property. The anti-inflammatory property was described in 1995, based on HDL's ability to block TNF-a-induced expression of the cellular adhesion molecules VCAM-1 and ICAM-1 in endothelial cells. Although numerous studies have confirmed this finding, the mechanism underlying this anti-inflammatory property remains unknown. I propose to focus on a new candidate for mediating HDL's anti-inflammatory property. Progranulin is a secreted growth factor that is expressed in many tissues and circulates in the blood. The progranulin gene, GRN, is mutated in some cases of familial frontotemporal dementia. Progranulin has been reported to be associated with HDL. Interestingly, recent studies revealed that progranulin binds to TNF receptors, thereby establishing a link between progranulin and inflammation. Specifically, current models posit that progranulin antagonizes TNF signaling by competing with TNF-a for binding to TNF receptors. Further, mice lacking progranulin have enhanced susceptibility to collagen-induced arthritis, illustrating functional consequences involving inflammation. This raises the intriguing hypothesis that progranulin significantly contributes to the anti-inflammatory property of HDL. Completion of these studies is expected to provide important insights into the molecular basis underlying HDL's anti-inflammatory property. Knowledge gleaned from these studies will likely have therapeutic implications for the prevention and treatment of cardiovascular disease. Moreover, it would be directly relevant to individuals with mutations in the GRN gene, which is mutated in some cases of frontotemporal dementia.
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海外基金