Type IX collagen knock-out mouse shows progressive hearing loss

被引:34
作者
Suzuki, N
Asamura, K
Kikuchi, Y
Takumi, Y
Abe, S
Imamura, Y
Hayashi, T
Aszodi, A
Fässler, R
Usami, S
机构
[1] Shinshu Univ, Sch Med, Dept Otorhinolaryngol, Matsumoto, Nagano 3908621, Japan
[2] Univ Tokyo, Inst Med Sci, Ctr Human Genome, Mol Med Lab,Minato Ku, Tokyo 1088639, Japan
[3] Univ Tokyo, Grad Sch Arts & Sci, Dept Life Sci, Tokyo 1538902, Japan
[4] Max Planck Inst Biochem, Dept Mol Med, D-85152 Martinsried, Germany
关键词
type IX collagen; type II collagen; knock-out mouse; progressive hearing loss; tectorial membrane; morphological change;
D O I
10.1016/j.neures.2004.12.001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Type IX collagen is one of the important components, together with type 11, V, and XI collagens, in the tectorial membrane of the organ of Corti. To confirm the significance of type IX collagen for normal hearing, we assessed the detailed morphological and electrophysiological features of type IX collagen knock-out mice, which have recently been reported as a deafness model. Through assessment by auditory brainstem response (ABR), knock-out mice were shown to have progressive hearing loss. At the light microscopic level, the tectorial membrane of knock-out mice was found to be abnormal in shape. These morphological changes started in the basal turn and were progressive toward the apical turn. Electron microscopy confirmed disturbance of organization of the collagen fibrils. These results suggest that mutations in type IX collagen genes may lead to abnormal integrity of collagen fibers in the tectorial membrane.(C) 2004 Elsevier Ireland Ltd and the Japan Neuroscience Society. All rights reserved.
引用
收藏
页码:293 / 298
页数:6
相关论文
共 23 条
[11]   An α-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21 [J].
Mustapha, M ;
Weil, D ;
Chardenoux, S ;
Elias, S ;
El-Zir, E ;
Beckmann, JS ;
Loiselet, J ;
Petit, C .
HUMAN MOLECULAR GENETICS, 1999, 8 (03) :409-412
[12]   An anatomically based frequency-place map for the mouse cochlea [J].
Ou, HC ;
Harding, GW ;
Bohne, BA .
HEARING RESEARCH, 2000, 145 (1-2) :123-129
[13]  
RICARDBLUM S, 2000, UNCONVENTIOANL COLLA, P73
[14]   A family with Stickler syndrome type 2 has a mutation in the COL11A1 gene resulting in the substitution of glycine 97 by valine in alpha 1(XI) collagen [J].
Richards, AJ ;
Yates, JRW ;
Williams, R ;
Payne, SJ ;
Pope, FM ;
Scott, JD ;
Snead, MP .
HUMAN MOLECULAR GENETICS, 1996, 5 (09) :1339-1343
[15]   Twister mutant mice are defective for otogelin, a component specific to inner ear acellular membranes [J].
Simmler, MC ;
Zwaenepoel, I ;
Verpy, E ;
Guillaud, L ;
Elbaz, C ;
Petit, C ;
Panthier, JJ .
MAMMALIAN GENOME, 2000, 11 (11) :961-966
[16]   LOCALIZATION OF TYPE-II, TYPE-IX AND TYPE-V COLLAGEN IN THE INNER-EAR [J].
SLEPECKY, NB ;
SAVAGE, JE ;
YOO, TJ .
ACTA OTO-LARYNGOLOGICA, 1992, 112 (04) :611-617
[17]   ELECTRON-MICROSCOPIC LOCALIZATION OF TYPE-II, IX, AND V COLLAGEN IN THE ORGAN OF CORTI OF THE GERBIL [J].
SLEPECKY, NB ;
SAVAGE, JE ;
CEFARATTI, LK ;
YOO, TJ .
CELL AND TISSUE RESEARCH, 1992, 267 (03) :413-418
[18]   TYPE-II AND TYPE-IX COLLAGEN FORM HETEROTYPIC FIBERS IN THE TECTORIAL MEMBRANE OF THE INNER-EAR [J].
SLEPECKY, NB ;
CEFARATTI, LK ;
YOO, TJ .
MATRIX, 1992, 12 (01) :80-86
[19]  
Verhoeven K, 1997, AM J HUM GENET, V60, P1168
[20]   AUTOSOMAL-DOMINANT AND RECESSIVE OSTEOCHONDRODYSPLASIAS ASSOCIATED WITH THE COL11A2 LOCUS [J].
VIKKULA, M ;
MARIMAN, ECM ;
LUI, VCH ;
ZHIDKOVA, NI ;
TILLER, GE ;
GOLDRING, MB ;
VANBEERSUM, SEC ;
MALEFIJT, MCD ;
VANDENHOOGEN, FHJ ;
ROPERS, HH ;
MAYNE, R ;
CHEAH, KSE ;
OLSEN, BR ;
WARMAN, ML ;
BRUNNER, HG .
CELL, 1995, 80 (03) :431-437