Genetic Modulation of Noise Injury to the Cochlear Lateral Wall

噪声对耳蜗外侧壁损伤的基因调控

• 批准号: 7413348
• 负责人: KEVIN K. OHLEMILLER
• 金额: $ 31.88万
• 依托单位: WASHINGTON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-04-20 至 2010-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7413348
• 关键词: 3-nitropropionic acid; Acute; Affect; Antioxidants; Auditory Threshold; Backcrossings; CBA/CaJ Mouse; CBA/J Mouse; Candidate Disease Gene; Cell Respiration; Cells; Characteristics; Chromosomes, Human, Pair 2; Cochlea; Cochlear duct; Code; Diagnosis; Environment; Epithelial Cells; Event; Exhibits; Generations; Genes; Genetic; Genome; Goals; Hearing; Heat shock proteins; Homeostasis; Homologous Gene; Hour; Human; Hybrids; Hypoxia; Inbred CBA Mice; Injury; Intervention; Ion Channel; Ion Pumps; Ion Transport; Ions; Iron-Regulatory Proteins; Knowledge; Lateral; Ligaments; Link; Literature; Maps; Measurement; Metric; Modification; Mus; Na(+)-K(+)-Exchanging ATPase; Noise; Noise-Induced Hearing Loss; Ouabain; Oxidation-Reduction; Oxidative Stress; Parents; Pathology; Phenotype; Pilot Projects; Play; Presbycusis; Process; Processed Genes; Public Health; Quantitative Trait Loci; Reactive Oxygen Species; Recombinants; Research; Research Personnel; Resistance; Role; Sensory; Severities; Stereocilium; Stress; Stria Vascularis; Testing; Time; Work; base; cell injury; cell type; cellular pathology; congenic; eumelanin; follow-up; gene discovery; hearing impairment; insight; novel; pheomelanin; programs; repaired; response; segregation; sound

DESCRIPTION (provided by applicant): We and others have identified several genes that promote cochlear noise injury in mice, and whose homologues may promote similar injury in humans. We now have evidence for a major effect quantitative trait locus (QTL) in mice that influences not the extent of noise injury, but rather the cellular distribution of noise injury. Hours after a moderate noise exposure (4-45 kHz, 110 dB SPL, 2 hrs), CBA/J mice show a reduction in the endocochlear potential (EP), as well as characteristic pathology within stria vascularis, spiral ligament, and spiral limbus. Although the EP recovers over time, the injury to stria and limbus is permanent. C57BL/6J (B6) mice, by contrast, show no significant acute EP reduction, and minimal acute or permanent cellular pathology. B6/CBA F1 hybrid mice respond to noise in a manner similar to the CBA parent strain, suggesting that one or a few dominant loci govern all facets of the injury phenotype. N2 backcross mice show the same constellation of noise pathology, and suggest linkage of the noise phenotype to the region containing the agouti locus on mouse chromosome 2. We HYPOTHESIZE that the linkage interval includes a gene involved in ion transport through the lateral stria (basal and intermediate cells) and limbus. The gene may code for an ion channel whose conductance is down-regulated by hypoxia or oxidative stress. Our findings point to novel genetic modulation of cochlear ion homeostasis during noise stress. The gene(s) and processes involved may impact the long term stability of cochlear noise injury and the accumulation of injury that presents as presbycusis. Our SPECIFIC AIMS are 1) To determine the cellular basis of EP reduction after noise exposure in CBA mice, 2) To examine the correlation of noise-related cellular pathologies of stria, spiral ligament, and limbus that comprise the CBA phenotype, and 3) To identify candidate gene(s) underlying CBA versus B6 strain differences in the effects of noise. RELEVANCE TO PUBLIC HEALTH: The cochlea contains many cell types whose functions are not known, but probably help maintain an appropriate ionic environment so that sensory cells can survive and respond sensitively to sound. Our work points to one or more genes that profoundy impact the distribution of noise injury in non-sensory cells. The gene, and the processes in which it is involved, may affect the long-term stability of cochlear injury, and the accumulation of injury that may be diagnosed as presbycusis.

描述（由申请人提供）：我们和其他人已经确定了几个促进小鼠耳蜗噪声损伤的基因，其同源物可能会促进人类类似的损伤。我们现在有证据表明，数量性状位点（QTL）在小鼠中的主要作用不是影响噪声损伤的程度，而是影响噪声损伤的细胞分布。中等噪声暴露（4-45 kHz, 110 dB SPL， 2小时）数小时后，CBA/J小鼠耳蜗内电位（EP）降低，血管纹、螺旋韧带和螺旋缘内的特征性病理改变。虽然EP会随着时间的推移而恢复，但纹状体和边缘的损伤是永久性的。相比之下，C57BL/6J （B6）小鼠没有明显的急性EP降低，也没有出现急性或永久性的细胞病理。B6/CBA F1杂交小鼠对噪音的反应方式与CBA亲本菌株相似，表明一个或几个显性位点控制着损伤表型的所有方面。N2回交小鼠显示出相同的噪声病理，并提示噪声表型与小鼠2号染色体上包含agouti位点的区域有关。我们假设连锁区间包括一个参与离子通过侧纹（基底细胞和中间细胞）和边缘运输的基因。该基因可能编码离子通道，其电导率因缺氧或氧化应激而下调。我们的发现指出了噪声胁迫下耳蜗离子稳态的新的遗传调节。所涉及的基因和过程可能影响耳蜗噪声损伤的长期稳定性和损伤的积累，表现为老年性耳蜗损伤。我们的具体目标是：1)确定CBA小鼠噪声暴露后EP降低的细胞基础；2)检查构成CBA表型的纹状、螺旋韧带和边缘与噪声相关的细胞病理的相关性；3)确定CBA和B6菌株在噪声影响下差异的候选基因。与公共卫生相关：耳蜗包含许多类型的细胞，其功能尚不清楚，但可能有助于维持适当的离子环境，使感觉细胞能够存活并对声音作出敏感反应。我们的工作指出了一个或多个基因对非感觉细胞中噪音损伤的分布有深远的影响。该基因及其参与的过程可能影响耳蜗损伤的长期稳定性，以及可能被诊断为老年性耳蜗损伤的损伤积累。