Mechanisms linking mitochondrial form and function
连接线粒体形式和功能的机制
基本信息
- 批准号:10205864
- 负责人:
- 金额:$ 53.01万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2021
- 资助国家:美国
- 起止时间:2021-05-01 至 2022-04-30
- 项目状态:已结题
- 来源:
- 关键词:AddressBehaviorCell DeathCell physiologyCellsDNA copy numberDiabetes MellitusDiseaseEukaryotic CellGenomeGiant CellsHealthHereditary DiseaseHomeostasisHumanHuman bodyInner mitochondrial membraneLinkMalignant NeoplasmsMetabolicMetabolic syndromeMetabolismMitochondriaMitochondrial DNANatural ImmunityNerve DegenerationNeurodegenerative DisordersObesityOrganellesOxidative PhosphorylationPathogenesisRegulationResearchRoleSignal PathwayWorkcell behaviorinsightmitochondrial dysfunctiontransmission process
项目摘要
Summary
Mitochondria are endosymbiotic organelles and have retained a reduced genome
packaged into 100-1000 copies of nucleoids per cell, distributed within dynamic
mitochondria “syncytia”. Mitochondria are the metabolic hubs of eukaryotic cells, producing
ATP via oxidative phosphorylation and other critical building blocks. They have evolved to
behave dynamically and to be an integrating platform for the assembly and regulation of
signaling pathways, such as cell death and innate immunity. Given their central roles, it is
not surprising that that mitochondrial dysfunction is associated with an increasingly large
proportion of human inherited disorders and with common diseases, such as
neurodegenerative disorders, metabolic syndromes, and cancer. To gain insight into the
roles of mitochondria in sickness and in health, we are focused on how mitochondrial
behavior is controlled within cells and how this behavior is intertwined with metabolism and
cell behavior. Our current research addresses the outstanding questions of how
mitochondrial DNA copy number and transmission is controlled in cells, how the
mitochondrial inner membrane is differentiated into distinct domains and how mitochondrial
behavior, metabolism and cell behavior are integrated. Addressing these questions will
illuminate how mitochondria contribute to cellular homeostasis and pathogenesis.
总结
线粒体是内共生的细胞器,
每个细胞包装成100-1000个类核拷贝,分布在动态
线粒体“合胞体”。线粒体是真核细胞的代谢中心,
ATP通过氧化磷酸化和其他关键的构建块。它们已经进化到
动态行为,成为组装和监管的集成平台
信号通路,如细胞死亡和先天免疫。鉴于其核心作用,
这并不奇怪,线粒体功能障碍与越来越大的
人类遗传性疾病和常见疾病的比例,如
神经变性病症、代谢综合征和癌症。为了深入了解
线粒体在疾病和健康中的作用,我们专注于线粒体如何
行为是在细胞内控制的,以及这种行为如何与新陈代谢交织在一起,
细胞行为我们目前的研究解决了悬而未决的问题,
线粒体DNA拷贝数和传输是在细胞中控制的,
线粒体内膜分化成不同的结构域,
行为、代谢和细胞行为是一体的。解决这些问题将
阐明线粒体如何有助于细胞内稳态和发病机制。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Jodi M. Nunnari其他文献
Mitochondrial Fission is Mediated by Conformational Changes in the Dynamin-related Protein, Dnm1
- DOI:
10.1016/j.bpj.2008.12.2105 - 发表时间:
2009-02-01 - 期刊:
- 影响因子:
- 作者:
Jason A. Mears;Laura L. Lackner;Shunming Fang;Jodi M. Nunnari;Jenny E. Hinshaw - 通讯作者:
Jenny E. Hinshaw
Jodi M. Nunnari的其他文献
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{{ truncateString('Jodi M. Nunnari', 18)}}的其他基金
Mechanisms linking mitochondrial form and function
连接线粒体形式和功能的机制
- 批准号:
10389944 - 财政年份:2021
- 资助金额:
$ 53.01万 - 项目类别:
Molecular basis and cellular roles of mitochondria-ER contact sites
线粒体-ER接触位点的分子基础和细胞作用
- 批准号:
10189369 - 财政年份:2011
- 资助金额:
$ 53.01万 - 项目类别:
Mechanisms controlling mitochondrial division and positioning
控制线粒体分裂和定位的机制
- 批准号:
8462640 - 财政年份:2011
- 资助金额:
$ 53.01万 - 项目类别:
Mechanisms controlling mitochondrial division and positioning
控制线粒体分裂和定位的机制
- 批准号:
8087874 - 财政年份:2011
- 资助金额:
$ 53.01万 - 项目类别:
Mechanisms controlling mitochondrial division and positioning
控制线粒体分裂和定位的机制
- 批准号:
8655901 - 财政年份:2011
- 资助金额:
$ 53.01万 - 项目类别:
Mechanisms controlling mitochondrial division and positioning
控制线粒体分裂和定位的机制
- 批准号:
8320081 - 财政年份:2011
- 资助金额:
$ 53.01万 - 项目类别:
The Mechanism of Mitochondrial Fission and Fusion.
线粒体裂变和融合的机制。
- 批准号:
7835146 - 财政年份:2009
- 资助金额:
$ 53.01万 - 项目类别:
A Tri-modular TIRF/Live Cell Confocal/Fast Widefield Fluorescence Imaging System
三模块 TIRF/活细胞共焦/快速宽场荧光成像系统
- 批准号:
7388456 - 财政年份:2008
- 资助金额:
$ 53.01万 - 项目类别:
Chemical Genetic Screens for Mitochondrial Division and Fusion Inhibitors
线粒体分裂和融合抑制剂的化学遗传筛选
- 批准号:
7305461 - 财政年份:2007
- 资助金额:
$ 53.01万 - 项目类别:
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