Neuroprotective Activity of DJ-1 in Parkinson's Disease
Neuroprotective Activity of DJ-1 in Parkinson's Disease
批准号:
7883233
负责人:
M. Maral Mouradian
金额:
$33.78万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-08-01 至 2012-06-30
关键词:
AccountingAddressAffectAmino Acid SubstitutionAntioxidantsApoptoticBindingBiochemicalBiologicalBiologyBrainCell DeathCell Death Signaling ProcessCell NucleusCell SurvivalCell modelCellsCessation of lifeCytoplasmDataDefectDiseaseEventFailureGene ActivationGene SilencingGenesGeneticGenetic TranscriptionGenetically Engineered MouseGoalsIndividualInheritedInvestigationKnockout MiceLeadLifeLightLinkMAP3K5 geneMediatingMolecularMolecular and Cellular BiologyMutateMutationNeuronsOxidantsOxidative StressPARK7 proteinParkinson DiseasePathogenesisPathway interactionsPhosphotransferasesPlayPoint MutationProcessPropertyProteinsReactive Oxygen SpeciesResearch PersonnelResistanceRoleSignal PathwayTestingTherapeutic InterventionWild Type Mousealpha synucleinbrain celldisease-causing mutationdopaminergic neurongene repressiongenetic pedigreein vivoin vivo Modelloss of functionmouse modelmutantneuronal survivaloxidant stressoxidative damagepreventprogramsresponsetransmission process
中文摘要
描述(由申请人提供):在过去十年中,几种遗传形式的帕金森病(PD)的遗传特征使得能够进行关于多巴胺能神经元存活的分子决定因素的机制研究,这些神经元对内源性和外源性损伤的反应,以及它们在这种疾病中的死亡。DJ-1是迄今为止被确定与遗传性PD相关的五个基因之一。在受影响的家系中,在DJ-1基因座中鉴定的两个原始突变的隐性传递表明,正常的DJ-1在多巴胺能神经元中起神经保护分子的作用,并且这种性质随着引起疾病的突变而丧失。本申请提出阐明这些神经保护机制,并解决这些过程中的扰动如何导致PD。第一个具体目标是扩展我们最近的发现,即野生型DJ-1抑制Daxx/ASK 1死亡信号通路,研究DJ-1中的各种突变如何影响这种凋亡机制,以及DJ-1的抗氧化功能如何使用细胞模型与该通路相关。第二个具体目标将解决该途径在PD受试者和基因工程小鼠脑中的体内相关性。第三个具体目标集中在DJ-1的细胞保护功能,通过调节基因的转录,这些基因是多巴胺能神经元通过Daxx依赖性和Daxx非依赖性机制存活的关键。这些研究的最终目的是通过确定治疗干预的潜在靶点来减轻帕金森病的负担,这些靶点也可以使散发性PD受益。DJ-1基因突变是遗传性帕金森病的原因之一。该项目的目标是了解DJ-1的正常功能,以及这些功能的缺陷如何导致大脑中的神经细胞变性。澄清这些事件可以帮助开发可能减缓或阻止脑细胞死亡的治疗方法。
英文摘要
DESCRIPTION (provided by applicant): The genetic characterization of several inherited forms of Parkinson's disease (PD) in the past decade has allowed the conduct of mechanistic studies about the molecular determinants of dopaminergic neuronal survival, the response of these neurons to endogenous and exogenous insults, and their demise in this disease. DJ-1 is one of five genes identified thus far to be linked to inherited PD. The recessive transmission of the two original mutations identified in the DJ-1 locus in affected pedigrees suggests that normal DJ-1 functions as a neuroprotective molecule in dopaminergic neurons, and that this property is lost with the disease causing mutations. This application proposes to elucidate these neuroprotective mechanisms and to address how perturbations in these processes lead to PD. The first specific aim proposes to expand on our recent discovery that wild-type DJ-1 inhibits the Daxx/ASK1 death signaling pathway, to investigate how various mutations in DJ-1 influence this apoptotic mechanism, and how the anti-oxidant function of DJ-1 relates to this pathway using cellular models. The second specific aim will address the in vivo relevance of this pathway in the brains of PD subjects and of genetically engineered mice. And the third specific aim focuses on the cytoprotective function of DJ-1 by modulating transcription of genes that are key to the survival of dopaminergic neurons both through Daxx-dependent and Daxx-independent mechanisms. The ultimate objective of these studies is to ease the Parkinson's disease burden by identifying potential targets for therapeutic interventions that can also benefit sporadic PD. For Lay public: Mutations in the DJ-1 gene is one of the causes of inherited Parkinson's disease. The goal of this project is to understand the normal functions of DJ-1 and how defects in these functions lead to nerve cell degeneration in the brain. Clarifying these events can help develop treatments that could potentially slow down or block brain cell death.
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