Giant Mitochondria in Aging
Giant Mitochondria in Aging
批准号:
8216930
负责人:
EDGAR A ARRIAGA
金额:
$4.51万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-04-15 至 2012-03-31
关键词:
3-methyladenineAffectAgingAlcoholismAmino AcidsAppearanceAutophagocytosisBiologicalBiological AgingCapillary ElectrophoresisCell Culture TechniquesCell modelCellsCellular biologyCentrifugationCharacteristicsCollaborationsConfocal MicroscopyDefectDiseaseElectron MicroscopyElectrophoresisFiberFluorescence MicroscopyFundingGene MutationGenomicsGoalsHealthHumanHyperoxiaIndividualKnowledgeLabelLinkLiteratureMembrane PotentialsMethodsMitochondriaMitochondrial DNAMitoticModelingMolecularMuscleMuscle FibersMuscle functionMyoblastsOrganellesPerformancePreparationPrincipal InvestigatorProceduresProductionPropertyProteinsProteomeProteomicsPublic HealthRattusRelative (related person)ReportingResearchResourcesRoleSamplingScientistSkeletal MuscleStable Isotope LabelingTechniquesTechnologyTimeTissuesToxic effectWorkage groupage relatedbasein vivomuscle agingnew technologynovelprotein expressiontheoriestool
中文摘要
描述(由申请人提供):有重要的证据表明线粒体与生物衰老有关,最近的一项理论表明,巨大的线粒体参与了有丝分裂后组织的衰老。在这些组织中,巨大的线粒体似乎逃避了自噬作用,积累并取代了正常的线粒体。在正常线粒体存在的情况下或从正常线粒体中分离出来后,描述巨大线粒体的技术是非常必要的。这项提议的短期目标是表征和分离巨型线粒体,并确定这些线粒体是否影响肌肉功能。长期目标是使用并提供新的技术方法,以揭示在亚细胞和分子水平上定义生物人类衰老的变化。这项拟议的工作利用了成肌细胞模型中的线粒体和费舍尔344只大鼠的肌肉。我们有四个目标:(1)基于细胞生物学,在活体细胞模型中描述巨大线粒体的特征。(2)从这些活体细胞模型中分离纯化出巨型线粒体,并对其进行生化鉴定。(3)比较从这些模型中分离的巨大线粒体和正常线粒体的蛋白质组。(4)骨骼肌衰老过程中巨大线粒体的特征。第一个目的是使用共聚焦显微镜,或结合单细胞毛细管电泳法,研究DNA的大小、DNA含量和合成、DNA突变、羰基积累、ROS产生、膜电位、线粒体融合和自噬作用。第二个目标描述了用自由流动电泳法分离巨型和正常线粒体亚群的方法,然后用适合于分离细胞器的方法对这些分离的线粒体进行表征。第三个目的是利用细胞培养中的稳定同位素标记来比较巨型和正常线粒体的蛋白质组。最后一个目的是研究含有巨大线粒体的肌肉中与年龄相关的变化。
对健康的意义。巨大线粒体的特征仍然很差,它们的蛋白质组和基因组特征还没有确定,它们与肌肉功能的关系也没有被研究过。这类线粒体的特征与公共健康高度相关,不仅因为它们可能在组织衰老中发挥作用,而且因为它们作为酒精中毒、人类毒性和多种疾病的结果而出现。
英文摘要
DESCRIPTION (provided by applicant): There is significant evidence linking mitochondria to biological aging, with a recent theory proposing that giant mitochondria are involved in the aging of post-mitotic tissues. In these tissues, giant mitochondria appear to evade autophagocytosis, accumulate, and replace normal mitochondria. Techniques to characterize giant mitochondria in the presence of, or after isolation from, normal mitochondria are greatly needed. The short- term goal of this proposal is to characterize and isolate giant mitochondria and establish whether or not these mitochondria affect muscle function. The long-term goal is to use and make available novel technological approaches for uncovering the changes that, at the subcellular and molecular level, define biological human aging. The proposed work utilizes mitochondria from a myoblast model and muscle from Fischer 344 rats. We have four aims: (1) Characterize giant mitochondria in vivo in cell models based on their cell biology. (2) Purify giant mitochondria isolated from these in vivo cell models and then characterize these giant mitochondria biochemically. (3) Compare the proteomes of giant and normal mitochondria isolated from these models. (4) Characterize giant mitochondria in aging skeletal muscle. The first aim uses confocal microscopy, or this technique combined with single cell capillary electrophoresis, to investigate size, DMA content and synthesis, DNA mutations, carbonyl accumulation, ROS production, membrane potential, mitochondrial fusion, and autophagocytosis. The second aim describes the methods to isolate subpopulations of giant and normal mitochondria using free-flow electrophoresis and then characterize these isolated mitochondria using methods suitable for isolated organelles. The third aim utilizes stable isotope labeling in cell cultures to compare the proteomes of giant and normal mitochondria. The last aim investigates age-related changes in muscle containing giant mitochondria.
Significance to Health. Giant mitochondria remain poorly characterized, their proteomic and genomic characteristics have not been defined, and their relationship to muscle function has not been investigated. The characterization of this class of mitochondria is highly relevant to the public health not only because of their possible role in aging tissues, but also because of their appearance as a consequence of alcoholism, human toxicity, and multiple diseases.
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会议论文
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