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突变型忙碌(BUS/Idr)小鼠前庭感觉细胞上的退行性小毛

Degenerative hairlets on the vestibular sensory cells in mutant bustling (BUS/Idr) mice.

作者信息

Moriyama K, Hashimoto R, Hanai A, Yoshizaki N, Yonezawa S, Otani H

机构信息

Department of Anatomy, Shimane Medical University, Izumo, Japan.

出版信息

Acta Otolaryngol. 1997 Jan;117(1):20-4. doi: 10.3109/00016489709117985.

DOI:10.3109/00016489709117985
PMID:9039475
Abstract

The bustling mouse (BUS/Idr: bus) is a mutant mouse strain which exhibits deafness, bustling/hyperkinetic behaviour and functional disorders seemingly related to the vestibular system. This phenotype develops in homozygous (bus/bus) mice and has been shown from cross experiments to be genetically induced by a single autosomal recessive gene. We previously detected, with light and electron microscopy, post-natal degeneration of the inner ear sensory cells in homozygotes. In the present study, we examined, by electron microscopy, the development of pathological changes in the sensory epithelia of the macula acustica and crista ampullaris of homozygous mice of various ages, paying special attention to the detailed morphology of the sensory hairlets. The homozygous mice exhibited specific pathological changes: a decrease in the number of hairs; disarrangement of the kinocilium-stereocilia pattern; and, fused and/or very large stereocilia. Homozygotes also frequently exhibited apical cytoplasmic herniation, or bleb of hair cells, as well as a degenerated kinocilium in the sensory epithelium. Heterozygotes showed similar changes, but to a lesser degree and frequency. As for the vestibular organs, similar pathological changes had developed at day, 17 of gestation. These pathological findings and onset suggest that the BUS mouse may be a mutant mouse strain distinct from other reported strains which display similar behaviour, and may be a useful animal model for the study of human degenerative vestibular disorders.

摘要

忙碌小鼠(BUS/Idr:bus)是一种突变小鼠品系,表现出耳聋、忙碌/多动行为以及似乎与前庭系统相关的功能障碍。这种表型在纯合子(bus/bus)小鼠中出现,并且通过杂交实验表明是由单个常染色体隐性基因遗传诱导的。我们之前通过光学显微镜和电子显微镜检测到纯合子内耳感觉细胞的产后退化。在本研究中,我们通过电子显微镜检查了不同年龄纯合小鼠听斑和壶腹嵴感觉上皮细胞病理变化的发展情况,特别关注了感觉纤毛的详细形态。纯合子小鼠表现出特定的病理变化:毛发数量减少;动纤毛 - 静纤毛模式紊乱;以及融合和/或非常大的静纤毛。纯合子还经常出现顶端细胞质疝出或毛细胞泡,以及感觉上皮中退化的动纤毛。杂合子表现出类似的变化,但程度和频率较低。至于前庭器官,在妊娠第17天时就已经出现了类似的病理变化。这些病理发现和发病情况表明,BUS小鼠可能是一种与其他报道的表现出类似行为的品系不同的突变小鼠品系,并且可能是研究人类退行性前庭疾病的有用动物模型。

相似文献

1
Degenerative hairlets on the vestibular sensory cells in mutant bustling (BUS/Idr) mice.突变型忙碌(BUS/Idr)小鼠前庭感觉细胞上的退行性小毛
Acta Otolaryngol. 1997 Jan;117(1):20-4. doi: 10.3109/00016489709117985.
2
Vestibulocochlear defects and effects of deuterium oxide in mutant bustling (BUS) mice.
Acta Otolaryngol Suppl. 1995;519:286-93. doi: 10.3109/00016489509121925.
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Hair cells in the inner ear of the pirouette and shaker 2 mutant mice.旋转和颤抖2突变小鼠内耳中的毛细胞。
J Neurocytol. 2000 Apr;29(4):227-40. doi: 10.1023/a:1026515619443.
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Morphologically specific vestibular hair cell degeneration in the jerker mouse mutant.急动小鼠突变体中形态学上特定的前庭毛细胞变性。
Eur Arch Otorhinolaryngol. 1990;247(1):51-5. doi: 10.1007/BF00240951.
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Cochlear histopathology of the mutant bustling mouse, BUS/Idr.突变型活泼小鼠(BUS/Idr)的耳蜗组织病理学
Acta Otolaryngol. 1996 May;116(3):409-16. doi: 10.3109/00016489609137865.
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Chromosomal localization of a gene responsible for vestibulocochlear defects of BUS/Idr mice: identification as an allele of waltzer.导致BUS/Idr小鼠前庭蜗缺陷的基因的染色体定位:鉴定为waltzer的一个等位基因。
Hear Res. 1999 Aug;134(1-2):116-22. doi: 10.1016/s0378-5955(99)00080-5.
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Vestibular morphology in relation to age and circling behavior.与年龄和转圈行为相关的前庭形态
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A morphological study on vestibular sensory epithelia in a strain of the waltzing guinea pig.
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Genetically induced inner ear degeneration. A structural and functional study.基因诱导的内耳退变:一项结构与功能研究
Acta Otolaryngol Suppl. 1992;493:141-6.
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Auditory and vestibular defects in the circling (ci2) rat mutant.转圈(ci2)大鼠突变体中的听觉和前庭缺陷。
Eur J Neurosci. 2001 Oct;14(7):1129-42. doi: 10.1046/j.0953-816x.2001.01726.x.

引用本文的文献

1
Genetics of peripheral vestibular dysfunction: lessons from mutant mouse strains.外周前庭功能障碍的遗传学:来自突变小鼠品系的经验教训。
J Am Acad Audiol. 2014 Mar;25(3):289-301. doi: 10.3766/jaaa.25.3.8.
2
Kbus/Idr, a mutant mouse strain with skeletal abnormalities and hypophosphatemia: identification as an allele of 'Hyp'.Kbus/Idr,一种具有骨骼异常和低血磷症的突变鼠品系:鉴定为“Hyp”的等位基因。
J Biomed Sci. 2011 Aug 20;18(1):60. doi: 10.1186/1423-0127-18-60.
3
A quantitative survey of gravity receptor function in mutant mouse strains.
突变小鼠品系重力感受器功能的定量研究。
J Assoc Res Otolaryngol. 2005 Dec;6(4):297-310. doi: 10.1007/s10162-005-0009-4.