Afferent Influences on Auditory System Ontogeny
传入对听觉系统个体发育的影响
基本信息
- 批准号:7782963
- 负责人:
- 金额:$ 47.31万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1999
- 资助国家:美国
- 起止时间:1999-05-01 至 2014-11-30
- 项目状态:已结题
- 来源:
- 关键词:AddressAffectAreaAuditoryAuditory areaAuditory systemBiologicalBiological MarkersBiological ModelsBirdsBrainBrain StemCalciumCell NucleusCellsCessation of lifeClinicalCochlear ImplantsCochlear nucleusCollaborationsCountryCouplingCytoskeletonDataDatabasesDendritesDevelopmentDiseaseElectrophysiology (science)ElectroporationEnvironmentEventExperimental GeneticsFundingFutureGene ExpressionGenesGenetic TranscriptionGenomeGlutamate ReceptorGoalsGrantGrowthHearingHomeostasisHumanImageIndividualInfantIntracellular TransportInvestigationKnowledgeLabelLabyrinthLeadLibrariesLinkMaintenanceMethodsMicroarray AnalysisMicroscopyMiningModificationMusMutationNeonatalNeonatal ScreeningNeuronsNeurosciencesOutcome AssessmentPMCA1 proteinPathologyPathway interactionsPatternPeripheralPlayPopulationPredispositionProteinsProteomicsQuality of lifeReceptor ActivationRegulationResearchResolutionResourcesRoleScienceSeriesSignal PathwayStructureSynapsesTechniquesTestingTimeTissuesWestern Blottingauditory pathwaycongenital deafnesscritical perioddeafnessdensitydeprivationearly onsetexperienceextracellularfascinategenetic analysisgenetic manipulationgenetic regulatory proteinhair cell regenerationhearing impairmentimaging modalityimmunoreactivityinformation processingmRNA Expressionmature animalmouse modelmutant mouse modelnerve supplyneuronal circuitryneuronal survivalneuroregulationpostnatalpresynapticprogramsprotein expressionpublic health relevancerehabilitation strategyrelating to nervous systemremediationresearch studyresponse
项目摘要
DESCRIPTION (provided by applicant): Understanding normal and abnormal brain development requires knowledge of the cellular events whereby differential experience influences the ontogeny of neural structure and function. Research in this area of auditory neuroscience has achieved a new level of clinical importance through universal newborn screening and enormously increased use of cochlear implants in congenitally and prelingually hearing impaired infants. This application seeks continued funding for a research program aimed at understanding the cellular events whereby the integrity and bioelectric activity of the inner influences development of brainstem auditory pathways. Two separate lines of investigation are proposed. 1. We will continue investigating the intercellular and intracellular signaling pathway(s) that underlie a critical period for susceptibility to neuronal death following the elimination of excitatory synaptic input to the mammalian cochlear nucleus. We propose a series of experiments to further examine developmental changes in transcription and protein expression in the murine cochlear nucleus over the period of hearing development. This pattern will be compared with data from similar analyses of cochlear nucleus tissue from several mutant mouse models of early onset inner ear structural and functional pathologies causing deafness. These studies will provide a library of biomarker profiles for better understanding of normal and hearing deprived cochlear nucleus development that can be used to assess disease states and attempts at remediation. 2. We combine single cell labeling, electrophysiology, calcium imaging and dynamic structural imaging methods to study the cellular pathways underlying afferent regulation of dendritic structure. We also test the hypothesis that a protein responsible for transporting intracellular calcium to the extracellular environment, PMCA2, is essential for maintenance of normal dendritic stability. These studies make use of the unique spatially segregated binaural innervation of n. laminaris cells to allow spatial resolution of the relationships between afferent stimulation, calcium homeostasis, calcium regulatory proteins and structural dynamics of dendrites.
PUBLIC HEALTH RELEVANCE: This project encompasses three interrelated areas: development of auditory information processing, neuroembryology of the auditory system, and the effects of experience on brain development. It is imperative that we understand how the various parts of the auditory system develop normally, in order to be able to therapeutically intervene in cases of congenital hearing loss. It is estimated that 10 to 20 percent of the US population have hearing impairments that significantly affect quality of life. Furthermore, 1 out of every 1,000 babies born in this country is seriously hearing impaired.
描述(由申请人提供):了解正常和异常的大脑发育需要了解细胞事件,从而差异经验影响神经结构和功能的个体发育。通过普遍的新生儿筛查和在先天性和语前听力受损的婴儿中大量增加使用人工耳蜗,听觉神经科学这一领域的研究在临床上的重要性达到了新的水平。该申请寻求继续资助一项研究计划,旨在了解细胞事件,从而内部的完整性和生物电活动影响脑干听觉通路的发展。提出了两条独立的调查路线。1.我们将继续研究细胞间和细胞内的信号通路(S)的基础上的一个关键时期的神经元死亡的敏感性消除兴奋性突触输入哺乳动物耳蜗核。我们提出了一系列的实验,以进一步研究在转录和蛋白质表达的小鼠耳蜗核在听力发育过程中的发展变化。这种模式将与来自耳蜗核组织的类似分析的数据进行比较,这些耳蜗核组织来自导致耳聋的早发性内耳结构和功能病理的几种突变小鼠模型。这些研究将提供一个生物标志物谱库,以更好地了解正常和听力剥夺的耳蜗核发育,可用于评估疾病状态和补救尝试。2.我们结合联合收割机单细胞标记、电生理学、钙离子成像和动态结构成像等方法来研究树突结构的传入调节的细胞通路。我们还测试了一种负责将细胞内钙转运到细胞外环境的蛋白质PMCA 2对维持正常树突稳定性至关重要的假设。这些研究利用了n独特的空间隔离双耳神经支配。laminaris细胞,以允许传入刺激,钙稳态,钙调节蛋白和树突的结构动力学之间的关系的空间分辨率。
公共卫生相关性:该项目包括三个相互关联的领域:听觉信息处理的发展,听觉系统的神经胚胎学,以及经验对大脑发育的影响。我们必须了解听觉系统的各个部分是如何正常发育的,以便能够在先天性听力损失的情况下进行治疗干预。据估计,10%至20%的美国人口患有严重影响生活质量的听力障碍。此外,在这个国家出生的每1,000名婴儿中就有一名听力严重受损。
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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Edwin W Rubel其他文献
Edwin W Rubel的其他文献
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{{ truncateString('Edwin W Rubel', 18)}}的其他基金
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ORC-13661预防静脉阿米卡星治疗非结核分枝杆菌感染患者耳毒性的有效性和安全性的2期研究
- 批准号:
10426862 - 财政年份:2022
- 资助金额:
$ 47.31万 - 项目类别:
Phase 2 Study of the Efficacy and Safety of ORC-13661 for the Prevention of Ototoxicity in Patients Receiving Intravenous Amikacin for Treatment of Non-Tuberculous Mycobacterium Infection
ORC-13661预防静脉阿米卡星治疗非结核分枝杆菌感染患者耳毒性的有效性和安全性的2期研究
- 批准号:
10706468 - 财政年份:2022
- 资助金额:
$ 47.31万 - 项目类别:
ROLE OF THE INNATE IMMUNE SYSTEM IN THE SURVIVAL OF AUDITORY NEURONS
先天免疫系统在听觉神经元生存中的作用
- 批准号:
10119786 - 财政年份:2017
- 资助金额:
$ 47.31万 - 项目类别:
Core Center--NIDCD Research Core Center P30
核心中心--NIDCD研究核心中心P30
- 批准号:
7901262 - 财政年份:2009
- 资助金额:
$ 47.31万 - 项目类别:
Core Center--NIDCD Research Core Center P30
核心中心--NIDCD研究核心中心P30
- 批准号:
6953304 - 财政年份:2000
- 资助金额:
$ 47.31万 - 项目类别:
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