The In Vivo Role of ERK1/2 Signaling in Peripheral Nervous System Development
The In Vivo Role of ERK1/2 Signaling in Peripheral Nervous System Development
批准号:
7788137
负责人:
Jason Marshall Newbern
金额:
$5.22万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-04-01 至 2011-03-31
关键词:
AddressAfferent NeuronsAllelesAxonBiological ModelsCell Differentiation processCell ProliferationClinicalComplexConflict (Psychology)DataDevelopmentDisciplineEmbryoExhibitsExtracellular MatrixFellowshipFinancial compensationGeneticGrowth FactorIn VitroMAPK1 geneMAPK3 geneMAPK7 geneMAPK7 geneMalignant NeoplasmsMediator of activation proteinMusMutationNatural regenerationNerve RegenerationNeuronsPathogenesisPathway interactionsPeripheralPeripheral Nervous SystemPlayPreparationProcessProteinsRoleSchwann CellsSignal TransductionSpinal GangliaStagingStimulusStudy modelsSyndromeTechnologyTrainingautism spectrum disorderaxon growthcell typecraniofacialextracellulargenetic analysisglial cell developmentin vivointerestmyelinationnervous system developmentpainful neuropathyprogramspromoterrecombinaseresearch studyresponsetherapeutic target
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The Extracellular signal-Regulated protein Kinase1/2 (ERK1/2, classical MARK) intracellular signal transduction cascade is activated by numerous extracellular stimuli that play important roles in various aspects of nervous system development, plasticity, and regeneration. Although ERK1/2 is thought to be vital for a number of processes its precise functional role has not been adequately analyzed. To better clarify the role of ERK1/2 signaling in peripheral nervous system development, we have utilized Cre/loxp technology to conditionally inactivate ERK1/2 specifically in sensory neurons and Schwann cells at early stages of development. The precise in vivo function of ERK1/2 signaling in Schwann cell differentiation and myelination and sensory neuron axon growth will be defined. The ability of the related kinase, ERK5, to compensate for loss of ERK1/2 will also be analyzed. These data will further our understanding of the complex functions regulated by ERK1/2 in separate cell types and clarify the intracellular pathways utilized by a trophic factors important for nervous system development. Summary Statement: Genetic or sporadic disruption of ERK1/2 signaling has been implicated in craniofacial syndromes, autism spectrum disorders, neuropathic pain, neurofibramatosis, and various cancers, yet our understanding of the functions of this pathway remain incomplete. The data arising from the execution of this proposal will be of interest to clinical disciplines; exploring ERK1/2 or ERK5 signaling as a therapeutic target, seeking to understand the pathogenesis of developmental syndromes resulting from mutations in regulators of ERK1/2 signaling, or attempting to reactivate neuronal or glial programs to induce or modify nervous system regeneration.
期刊论文(3)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1016/j.semcdb.2010.08.008
发表时间:
2010-12
期刊:
Seminars in cell & developmental biology
影响因子:
7.3
作者:
[Newbern J, Birchmeier C]
通讯作者:
Birchmeier C
Functions of ERK/MAPK Signaling in GABAergic Circuit Development
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批准号:9923769
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项目类别:
-
资助金额:$34.07万
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财政年份:2016
-
负责人:Jason Marshall Newbern
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依托单位:
ERK/MAPK regulation of cortical inhibitory interneurons
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批准号:8338802
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项目类别:
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资助金额:$8.7万
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财政年份:2011
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负责人:Jason Marshall Newbern
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依托单位:
ERK/MAPK regulation of cortical inhibitory interneurons
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批准号:8733171
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项目类别:
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资助金额:$24.09万
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财政年份:2011
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负责人:Jason Marshall Newbern
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依托单位:
ERK/MAPK regulation of cortical inhibitory interneurons
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批准号:8226226
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项目类别:
-
资助金额:$8.7万
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财政年份:2011
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负责人:Jason Marshall Newbern
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依托单位:
ERK/MAPK regulation of cortical inhibitory interneurons
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批准号:8703421
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项目类别:
-
资助金额:$24.7万
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财政年份:2011
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负责人:Jason Marshall Newbern
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依托单位:
The In Vivo Role of ERK1/2 Signaling in Peripheral Nervous System Development
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批准号:7676488
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项目类别:
-
资助金额:$5.01万
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财政年份:2009
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负责人:Jason Marshall Newbern
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依托单位:
海外基金