Microglial Phox Activity In Parkinson's Disease
Microglial Phox Activity In Parkinson's Disease
批准号:
8231458
负责人:
Jing Zhang
金额:
$34.75万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-03-01 至 2015-02-28
关键词:
4-ethoxymethylene-2-phenyl-2-oxazoline-5-oneAnimal ModelBacteriaDataDevelopmentDiseaseDopamineEnvironmental ExposureEnvironmental Risk FactorEnzymesExposure toFundingGeneticGenetic Predisposition to DiseaseHumanIn VitroInvestigationKnowledgeLinkLipopolysaccharidesMacrophage-1 AntigenMediatingMediator of activation proteinMembraneMicrogliaModelingMolecularNADPH OxidaseNerve DegenerationNeuraxisNeurodegenerative DisordersNeuronsParkinson DiseaseParkinsonian DisordersPathogenesisPathway interactionsPatientsProcessProteinsResearchResourcesRoleRotenoneTestingTherapeutic InterventionToxic Environmental SubstancesToxic effectUnited States National Institutes of HealthValidationWild Type Mousealpha synucleindesigndopamine systemdopaminergic neuronextracellularhuman tissuein vivoin vivo Modelkillingsmutantneuroinflammationneurotoxicneurotoxicitynew therapeutic targetpreventpublic health relevanceresponsesynucleintoxicant
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The role of microglial activation and neuroinflammation has recently emerged as a potential mediator and /or potentiator of Parkinson's disease (PD) pathogenesis. While the precise mechanisms and pathways responsible for neurodegeneration are relatively unclear, sufficient evidence has been put forth to suggest that PD has a multifactorial etiopathogenesis. Indeed, environmental as well as genetic factors have been demonstrated to cause activation of microglia, leading to neuroinflammation and subsequent damage to the nigrostriatal dopamine system. Furthermore, genetic and environmental insults both involve activation of NADPH oxidase (PHOX), a key mediator of the neurotoxic response following microglial activation. These data highlight the importance of PHOX and provides a common link between genetic susceptibility and environmental insult in the development of PD. Thus, this proposal will exploit the intersection of genetic and environmental factors at PHOX to gain a better understanding of the mechanisms involved in microglia- mediated neurotoxicity. Through the utilization of in vitro and in vivo models, the aims proposed will systematically elucidate the interplay between endogenous and exogenous insults and their synergistic contribution to microglial activation and neurodegeneration. Moreover, specific interacting proteins and pathways involved in these processes will be examined and these results will be further validated in human tissue from PD patients and compared to other neurodegenerative diseases. Completion of these proposed aims will provide a better understanding of the interaction of genetic and environmental factors at PHOX. Finally, the identification of specific proteins and pathways involved in microglia-mediated neurodegeneration may provide potential targets of therapeutic intervention for patients with PD.
PUBLIC HEALTH RELEVANCE: This project investigates the potential interplay between genetic vulnerability and environmental exposure that likely contributes to the development of the majority of Parkinson's cases. Elucidation of the mechanisms involved in this interplay may yield new therapies for the devastating disease.
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Dose-dependent Activation of the MEK/ERK Pathway in Hematopoiesis
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财政年份:2012
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Large Scale Biomarker Discovery and Validation for Parkinsons Disease
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财政年份:2012
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依托单位:
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项目类别:
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财政年份:2012
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依托单位:
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依托单位:
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