Kitamura K, Nomura Y, Yagi M, Yoshikawa Y, Ochikubo F
Department of Otolaryngology, University of Tokyo, Japan.
Acta Otolaryngol. 1991;111(1):61-9. doi: 10.3109/00016489109137355.
The hearing ability and histological characteristics of the cochlea of a strain of new-mutant mice were analyzed. This new mutant arose as a spontaneous mutation in the C3H/He stock. The genetic mode is autosomal recessive and the animals show abnormal behavior such as circling, head-tossing and hyperactivity. The audiological findings exhibited no recordable auditory brain stem response (ABR) in any homozygotes at ages ranging from 11 days to 117 days. For morphological examination, we used 36 homozygote with ages ranging from 10 days to 18 months. The primary morphological abnormalities were observed in the organ of Corti. The stereocilia of the outer hair cells showed disarray throughout the whole cochlea, although outer hair cell cytoplasm became fully developed, including the nerve terminals. Age-dependent degeneration of the outer hair cells subsequently occurred from the basal to the apical part of the cochlea. The earliest change demonstrated in the outer hair cells was cuticular degeneration. Although the abnormalities of the inner hair cells occurred late, a complete loss of inner and outer hair cells was demonstrated. The stria vascularis was well preserved at a later age as were spiral ganglion cells. These histological findings confirm that this mouse is classified as a neuroepithelial-type mutant. As this animal was expected to have a single gene abnormality, molecular genetic studies on this animal can provide important information on the nature of histological changes of the hair cell from a mode of gene action.
对一种新突变小鼠品系的耳蜗听力能力和组织学特征进行了分析。这种新突变是在C3H/He种群中自发产生的。遗传模式为常染色体隐性遗传,动物表现出异常行为,如转圈、甩头和多动。听力学检查结果显示,在11天至117天龄的任何纯合子中均未记录到可听性脑干反应(ABR)。为了进行形态学检查,我们使用了36只年龄在10天至18个月之间的纯合子。主要的形态学异常在柯蒂氏器中观察到。外毛细胞的静纤毛在整个耳蜗中都显示出排列紊乱,尽管外毛细胞的细胞质包括神经末梢已完全发育。随后,外毛细胞从耳蜗基部到顶部出现了年龄依赖性退变。外毛细胞最早出现的变化是表皮退变。尽管内毛细胞的异常出现较晚,但内、外毛细胞均出现了完全丧失。血管纹在后期保存良好,螺旋神经节细胞也是如此。这些组织学结果证实,这种小鼠被归类为神经上皮型突变体。由于预计这种动物有单一基因异常,对这种动物进行分子遗传学研究可以从基因作用模式提供关于毛细胞组织学变化性质的重要信息。