DOCK7 Signaling in Neuronal Development
DOCK7 Signaling in Neuronal Development
批准号:
8245088
负责人:
Linda Van Aelst
金额:
$41.77万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-07-01 至 2013-07-31
关键词:
ActinsAddressAdoptedAxonBiochemicalBiologicalBiological ModelsBrainCellsComplexDataDefectDendritesDetergentsDevelopmentElectroporationEventExtracellular Matrix ProteinsFailureFamilyFamily memberGenerationsGeneric DrugsGoalsGuanosine Triphosphate PhosphohydrolasesHealthHippocampus (Brain)HumanImmunofluorescence ImmunologicLamininLifeLinkMass Spectrum AnalysisMediatingMembraneMethodsMicroscopyMicrotubulesMolecularMonitorMorphologyMotorNatural regenerationNatureNerve RegenerationNervous system structureNeuritesNeurodegenerative DisordersNeuronsPathway interactionsPhosphoproteinsPhosphorylationPhosphotransferasesPlayProcessProtein IsoformsProteinsRattusRegulationRoleSignal PathwaySignal TransductionSliceStem cellsStructureTechniquesTechnologyTherapeutic AgentsTwo-Hybrid System TechniquesWorkYeastsbasecell typecellular imagingcognitive functionexperiencegain of functiongenetic regulatory proteinin uteroinsightmembermigrationneuron developmentneuron lossnovelpolarized cellpolypeptiderho GTP-Binding Proteinsstathmintwo-photon
中文摘要
描述(由申请人提供):本研究的长期目标是了解轴突发育和神经元极性建立的分子和细胞机制。神经元细胞的极化能力对神经系统的组织至关重要,并具有深远的功能意义。典型的情况是,神经元极化形成一个长轴突和多个较短的树突,以传递和接收信息,并建立对正常认知功能至关重要的电路。此外,大量证据表明,神经元极性的丧失与许多神经退行性疾病有关。因此,了解神经元极化的机制对人类健康至关重要。建立极化神经元的初始事件是单个轴突的发育。我们最近发现DOCK7是一种新的Rac gtpase激活剂,并证明该蛋白在轴突发育的早期阶段起着至关重要的作用。此外,我们的数据揭示了DOCK7与微管调控蛋白stathmin之间的联系,并强调了微管网络调控对轴突发育的贡献。这些发现为获得轴突发育的分子和细胞基础的新见解提供了一个独特的框架。本应用程序旨在进一步描述DOCK7功能在这一重要发育步骤中的作用和机制。为了实现这些目标,第一个具体目标将描述介导DOCK7对安定素磷酸化和轴突发育影响的信号通路。具体目标2侧重于DOCK7的调控,包括DOCK7如何在新生轴突中被激活和选择性定位的机制。分子,生物化学和细胞生物学的方法将被用来解决这些目标。第三个具体目标是通过生化纯化技术和质谱技术以及酵母双杂交方法鉴定dock7相互作用蛋白,这些蛋白在神经元极化中发挥重要作用。最后,特异性目标4详细研究了DOCK7在脑切片中迁移皮层神经元极化中的作用。为此,将采用子宫内电穿孔技术和双光子显微镜。从这些研究中获得的信息将极大地有助于理解轴突发育和神经元极化的机制。因此,它们将对理解生物医学相关过程具有重要意义,包括神经元发育、相关认知功能、神经再生和神经退行性疾病。公共卫生相关性:神经元细胞的极化能力——即形成一个轴突和多个较短的树突——对神经系统的组织至关重要,对正常的认知功能和神经细胞的再生具有深远的功能影响。提出的研究旨在了解轴突发育和神经元极化的分子和细胞机制。因此,它们将对许多生物医学相关过程具有重要意义,包括神经元发育、相关认知功能、神经再生和神经退行性疾病,并可能为开发治疗新轴突和受损轴突的产生和再生的药物提供基础。
英文摘要
DESCRIPTION (provided by applicant): The long-term objective of this study is to understand the molecular and cellular mechanisms that underlie axon development and the establishment of neuronal polarity. The ability of neuronal cells to polarize is essential for the organization of the nervous system and has profound functional implications. Typically, a neuron polarizes to elaborate one long axon and multiple, shorter dendrites so as to transmit and receive information and establish the circuitry that is critical for normal cognitive functions. Moreover, abundant evidence indicates that loss of neuronal polarity is associated with numerous neurodegenerative diseases. Thus understanding the machineries involved in neuronal polarization is of utmost importance to human health. The initial event in establishing a polarized neuron is the development of a single axon. We have recently identified DOCK7 as a novel activator of Rac GTPases, and demonstrated that the protein plays a crucial role in early steps of axon development. Moreover, our data have unveiled a link between DOCK7 and the microtubule regulatory protein, stathmin, and highlight the contribution of microtubule network regulation to axon development. These findings provide a unique framework for obtaining novel insight into the molecular and cellular underpinnings of axon development. This application aims to delineate further the role and mechanism of DOCK7 function in this important developmental step. Towards these goals, the first specific aim will characterize the signaling pathway that mediates the effect of DOCK7 on stathmin phosphorylation and axon development. Specific aim 2 focuses on the regulation of DOCK7, including the mechanisms that define how DOCK7 becomes activated and selectively localized in the nascent axon. Molecular, biochemical, and cell biological approaches will be used to address these objectives. The third specific aim will identify DOCK7-interacting proteins important for its function in neuronal polarization, by using biochemical purification techniques and mass spectrometry, and the yeast two-hybrid method. Finally, specific aim 4 scrutinizes the role of DOCK7 in the polarization of migrating cortical neurons in brain slices. To this end, in utero electroporation technology and two-photon microscopy will be employed. Information gained from these studies will greatly contribute to understanding the mechanisms that underlie axon development and neuronal polarization. As such, they will have significant implications for understanding biomedically relevant processes, including neuronal development, associated cognitive function, nerve regeneration and neurodegenerative disease. PUBLIC HEALTH RELEVANCE: The ability of neuronal cells to polarize - i.e. to elaborate one axon and multiple, shorter dendrites - is essential for the organization of the nervous system and has profound functional ramifications for normal cognitive functions and the regeneration of nerve cells. The proposed studies are aimed at understanding the molecular and cellular mechanisms that underlie axon development and neuronal polarization. As such, they will have significant implications for numerous biomedically relevant processes, including neuronal development, associated cognitive function, nerve regeneration and neurodegenerative disease, and may provide the basis for developing therapeutic agents for the generation and regeneration of new and damaged axons, respectively.
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会议论文
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Rho regulator-mediated signaling in interneuron development
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资助金额:$48.18万
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财政年份:2013
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Role of Dok-1 in oncogenic tyrosine kinase signaling
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Role of Dok-1 in oncogenic tyrosine kinase signaling
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Role of Dok-1 in oncogenic tyrosine kinase signaling
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海外基金