Role of Mitochondrial DNA Mutations in Aging in Neuronal Cells
Role of Mitochondrial DNA Mutations in Aging in Neuronal Cells
批准号:
7568809
负责人:
Yidong Bai
金额:
$28.95万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-03-01 至 2011-01-31
关键词:
AgeAgingAging-Related ProcessApoptosisApplications GrantsBiochemicalBiogenesisBrainBrain regionCell Culture SystemCell LineCell modelCell physiologyCellsDNAElectron TransportEnergy SupplyEvaluationExhibitsFunctional disorderGene MutationGenerationsGenesGeneticGenetic TranscriptionGoalsIndividualLipidsMeasuresMethodsMitochondriaMitochondrial DNAMolecularMolecular GeneticsMonitorMusMutationNerve EndingsNeuroblastomaNeuronsNuclearOxidative PhosphorylationOxidative StressPhenotypePhysiologicalProteinsReactive Oxygen SpeciesRegulationRelative (related person)ReportingRespirationRoleSequence AnalysisSignal TransductionSynaptosomesSystemTechnologyTestingTimeTissuesTranslationsage groupage relatedestablished cell linehuman tissueimprovedinsightmiddle agemitochondrial DNA mutationmitochondrial dysfunctionmitochondrial genomemutantoxidative damageprogramsrespiratorytheories
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Our long-term goal is to study the role of mitochondria in aging. The overall goal of this grant application is to
test the mitochondria! theror/ of aging and, in particular, to investigate the role of mitochondrial DNA(mtDNA)
mutations in mouse brain during aging. As one of the most favored hypotheses, the mitochondrial theory of
aging, predicts that somatic mitochondria DNA (mtDNA) mutations accumulate with time, and the
compromised mitochondrial function resulting from these mutations is then responsible for various aging
phenotypes. However, there has been no comprehensive study of the overall accumulation of mtDNA
mutations during aging, and the physiological consequences of aging-related mtDNA mutations are largely
unclear. We recently established a method to transfer mtDNA from mouse nerve endings, i.e., synaptosomes
to a cell system, and we have improved methods to isolate and characterize mtDNA mutations. Combined with
established mitochondrial molecular genetic and biochemical technologies, we can, for the first time,
investigate the accumulation of mtDNA mutations in neuronal cells during aging by evaluating individual
mtDNA from the synaptosomes.The particular hypothesis to be tested in this proposal is that mutations in the
mitochondrial genome accumulate during aging in mouse neuronal cells; these mtDNA mutations in turn
compromise mitochondrial function and may result in oxidative damage to various cellular components
including mtDNA in neuronal cells. We will perform genetic and functional analyses of aging-related mtDNA
mutations by transferring synaptosomal mtDNA to a cell line system. This will reveal low frequncy mtDNA
mutations that could not be identified by other methods. By generating neuronal cell models that carry
aging-related mtDNA mutations, we will also charaterize the physiological consequences of the mutations, in
particular those related to oxidative damage. The successful completion of this project will not only help to test
the mitochondrial theory of aging, but could also provide insights into the underlying mechanisms of the aging
process.
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海外基金