Vijayakumar Sarath, Lever Teresa E, Pierce Jessica, Zhao Xing, Bergstrom David, Lundberg Yunxia Wang, Jones Timothy A, Jones Sherri M
Department of Special Education and Communication Disorders, University of Nebraska-Lincoln, 301 Barkley Memorial Center, Lincoln, NE, 68583, USA.
Mamm Genome. 2015 Apr;26(3-4):154-72. doi: 10.1007/s00335-015-9556-0. Epub 2015 Feb 3.
A/J mice develop progressive hearing loss that begins before 1 month of age and is attributed to cochlear hair cell degeneration. Screening tests indicated that this strain also develops early onset vestibular dysfunction and has otoconial deficits. The purpose of this study was to characterize the vestibular dysfunction and macular structural pathology over the lifespan of A/J mice. Vestibular function was measured using linear vestibular evoked potentials (VsEPs). Macular structural pathology was evaluated using light microscopy, scanning electron microscopy, transmission electron microscopy, confocal microscopy and Western blotting. Individually, vestibular functional deficits in mice ranged from mild to profound. On average, A/J mice had significantly reduced vestibular sensitivity (elevated VsEP response thresholds and smaller amplitudes), whereas VsEP onset latency was prolonged compared to age-matched controls (C57BL/6). A limited age-related vestibular functional loss was also present. Structural analysis identified marked age-independent otoconial abnormalities in concert with some stereociliary bundle defects. Macular epithelia were incompletely covered by otoconial membranes with significantly reduced opacity and often contained abnormally large or giant otoconia as well as normal-appearing otoconia. Elevated expression of key otoconins (i.e., otoconin 90, otolin and keratin sulfate proteoglycan) ruled out the possibility of reduced levels contributing to otoconial dysgenesis. The phenotype of A/J was partially replicated in a consomic mouse strain (C57BL/6J-Chr 17(A/J)/NaJ), thus indicating that Chr 17(A/J) contained a trait locus for a new gene variant responsible to some extent for the A/J vestibular phenotype. Quantitative trait locus analysis identified additional epistatic influences associated with chromosomes 1, 4, 9 and X. Results indicate that the A/J phenotype represents a complex trait, and the A/J mouse strain presents a new model for the study of mechanisms underlying otoconial formation and maintenance.
A/J小鼠在1月龄前就开始出现进行性听力丧失,这归因于耳蜗毛细胞变性。筛查测试表明,该品系还会出现早发性前庭功能障碍并有耳石缺陷。本研究的目的是描述A/J小鼠一生中的前庭功能障碍和黄斑结构病理学特征。使用线性前庭诱发电位(VsEPs)测量前庭功能。使用光学显微镜、扫描电子显微镜、透射电子显微镜、共聚焦显微镜和蛋白质免疫印迹法评估黄斑结构病理学。单独来看,小鼠的前庭功能缺陷程度从轻度到重度不等。平均而言,A/J小鼠的前庭敏感性显著降低(VsEP反应阈值升高且振幅较小),而与年龄匹配的对照(C57BL/6)相比,VsEP起始潜伏期延长。还存在有限的与年龄相关的前庭功能丧失。结构分析发现,与一些静纤毛束缺陷一致,存在明显的与年龄无关的耳石异常。黄斑上皮未被耳石膜完全覆盖,不透明度显著降低,且通常含有异常大或巨大的耳石以及外观正常的耳石。关键耳石蛋白(即耳石蛋白90、耳石素和硫酸角质素蛋白聚糖)的表达升高排除了其水平降低导致耳石发育异常的可能性。A/J的表型在一个染色体代换小鼠品系(C57BL/6J-Chr 17(A/J)/NaJ)中部分得到复制,因此表明Chr 17(A/J)包含一个新基因变体的性状位点,该变体在一定程度上导致了A/J的前庭表型。数量性状位点分析确定了与染色体1、4、9和X相关的其他上位性影响。结果表明,A/J表型代表一种复杂性状,A/J小鼠品系为研究耳石形成和维持的潜在机制提供了一个新模型。