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调节遗传异质性小鼠老年听力的等位基因。

Alleles that modulate late life hearing in genetically heterogeneous mice.

机构信息

Kresge Hearing Research Institute, Department of Otolaryngology, University of Michigan Medical School, Ann Arbor, MI, USA.

出版信息

Neurobiol Aging. 2012 Aug;33(8):1842.e15-29. doi: 10.1016/j.neurobiolaging.2011.12.034. Epub 2012 Feb 2.

Abstract

A genetically heterogeneous population of mice was tested for hearing at 8, 18, and 22 months by auditory brainstem response (ABR), and genotyped at 128 markers to identify loci that modulate late life hearing loss. Half of the test mice were exposed to noise for 2 hours at age 20 months. Polymorphisms affecting hearing at 18 months were noted on chromosomes 2, 3, 7, 10, and 15. Most of these loci had effects only on responses to 48 kHz stimuli, but a subset also influenced the auditory brainstem response at lower frequencies. Loci on chromosomes 4, 10, 12, and 14 had significant effects on hearing at 22 months in noise-exposed mice, and loci on chromosomes 10 and 11 had effects on mice not exposed to noise. Outer hair cell loss was modulated by polymorphisms on chromosomes 10, 11, 12, 17, and 19. Resistance to age-related hearing loss is thus modulated by a set of genetic effects, some age-specific, some frequency specific, some dependent on prior exposure to noise, and some of which compromise survival of cochlear hair cells.

摘要

一组遗传异质性的小鼠群体在 8、18 和 22 个月时通过听觉脑干反应(ABR)进行听力测试,并在 128 个标记处进行基因分型,以确定调节晚年听力损失的基因座。一半的测试小鼠在 20 个月大时暴露于 2 小时的噪声中。在 18 个月时影响听力的多态性出现在染色体 2、3、7、10 和 15 上。这些基因座中的大多数仅对 48 kHz 刺激的反应有影响,但一部分也影响低频的听觉脑干反应。在暴露于噪声的小鼠中,染色体 4、10、12 和 14 上的基因座对 22 个月时的听力有显著影响,而染色体 10 和 11 上的基因座对未暴露于噪声的小鼠有影响。外毛细胞的丧失受染色体 10、11、12、17 和 19 上的多态性调节。因此,年龄相关性听力损失的抗性受一组遗传效应调节,一些是年龄特异性的,一些是频率特异性的,一些取决于先前暴露于噪声,一些则影响耳蜗毛细胞的存活。

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