A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice

被引:49
作者
Zheng, Qing Yin [1 ,3 ]
Ding, Dalian [2 ]
Yu, Heping [1 ]
Salvi, Richard J. [2 ]
Johnson, Kenneth R. [3 ]
机构
[1] Case Western Reserve Univ, Dept Otolaryngol HNS, Cleveland, OH 44106 USA
[2] SUNY Buffalo, Ctr Hearing & Deafness, Buffalo, NY 14214 USA
[3] Jackson Lab, Bar Harbor, ME 04609 USA
关键词
Genetic mapping; Mouse; Inbred strain; Deafness; Presbycusis; QUANTITATIVE TRAIT LOCI; HAIR CELL LOSS; INBRED STRAINS; SUBSTITUTION STRAINS; COCHLEAR PATHOLOGY; ANIMAL-MODEL; MOUSE; GENE; PRESBYCUSIS; IMPAIRMENT;
D O I
10.1016/j.neurobiolaging.2007.12.011
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The ahl locus, shown to be a strain-specific Cdh23 dimorphism, contributes to age-related hearing loss in many inbred mouse strains. A/J mice begin to lose hearing by 4 weeks of age, much earlier than C57BL/6J (136) mice, although both strains have the same Cdh23(ahl) Variant. Here, we use recombinant inbred strains, chromosome substitution strains, and a linkage backcross to map a locus on distal Chromosome 10, designated ahl4, that contributes to the early-onset hearing loss of A/J mice. Cochleae of 9-week-old A/J mice exhibit inner and outer hair cell loss from the basal turn through the apical turn, with outer hair cell loss at the base being severest. To quantify the progression of hair cell loss, cytocochleograms were evaluated from 0 to 20 weeks of age. A/J mice showed evidence of hair cell loss in the base of the cochlea as early as 14 days of age and the magnitude and extent of loss increased rapidly during the following 2-5 months. Hair cell loss occurred earlier and was much more severe and widespread in A/J mice than in B6 mice during the first 5 months of age. Spiral ganglion neurons, cells of the stria vascularis, and vestibular hair cell densities, however, appeared normal in 20-week-old A/J mice. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:1693 / 1705
页数:13
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