MORPHOLOGICAL-CHANGES OF COCHLEA IN A STRAIN OF NEW-MUTANT MICE

被引:13
作者
KITAMURA, K
NOMURA, Y
YAGI, M
YOSHIKAWA, Y
OCHIKUBO, F
机构
[1] UNIV TOKYO,INST MED SCI,LAB ANIM RES CTR,TOKYO 113,JAPAN
[2] UNIV TOKYO,DEPT ANIM PATHOL,TOKYO 113,JAPAN
关键词
TRANSMISSION ELECTRON MICROSCOPE; SCANNING ELECTRON MICROSCOPE; HAIR CELL DEGENERATION; DEAF; AUDITORY BRAIN-STEM RESPONSE (ABR);
D O I
10.3109/00016489109137355
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
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.
引用
收藏
页码:61 / 69
页数:9
相关论文
共 16 条
[1]   THE AGING VESTIBULAR HAIR CELL [J].
ANNIKO, M .
AMERICAN JOURNAL OF OTOLARYNGOLOGY, 1983, 4 (03) :151-160
[2]   INNER-EAR PATHOLOGY IN THE DEAFNESS MUTANT MOUSE [J].
BOCK, GR ;
STEEL, KP .
ACTA OTO-LARYNGOLOGICA, 1983, 96 (1-2) :39-47
[3]  
Deol M S, 1968, J Med Genet, V5, P137, DOI 10.1136/jmg.5.2.137
[4]   SPINNER MOUSE [J].
DEOL, MS ;
ROBINS, MW .
JOURNAL OF HEREDITY, 1962, 53 (03) :133-&
[6]   SNELLS WALTZER A NEW MUTATION AFFECTING BEHAVIOUR AND INNER EAR IN MOUSE [J].
DEOL, MS ;
GREEN, MC .
GENETICAL RESEARCH, 1966, 8 (03) :339-&
[8]  
GRUNEBERG H, 1956, BRIT MED BULL, V12, P153
[9]  
Hultcrantz M, 1985, Acta Otolaryngol Suppl, V425, P1
[10]  
MIKAELIAN DO, 1964, ARCHIV OTOLARYNGOL, V80, P418