Resorption of auditory ossicles and hearing loss in mice lacking osteoprotegerin

被引:62
作者
Kanzaki, Sho
Ito, Masako
Takada, Yasunari
Ogawa, Kaoru
Matsuo, Koichi
机构
[1] Keio Univ, Sch Med, Dept Microbiol & Immunol, Shinjuku Ku, Tokyo 1608582, Japan
[2] Keio Univ, Sch Med, Dept Otolaryngol, Shinjuku Ku, Tokyo 1608582, Japan
[3] Nagasaki Univ, Sch Med, Dept Radiol, Nagasaki 8528501, Japan
基金
日本学术振兴会;
关键词
bone remodeling; osteoclast; osteoprotegerin; hearing loss; auditory ossicles;
D O I
10.1016/j.bone.2006.01.155
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bones conduct sound in the middle ear. The three ossicles-the malles, incus, and stapes-form a chain that transmits vibrations from the tympanic membrane to the oval window of the inner ear. Little is known about bone remodeling events in these ossicles and about potential effects of osteoporosis on hearing loss. Osteoclastic bone resorption is enhanced in Opg(-/-) mice lacking osteoprotegerin, which is a soluble decoy receptor for the osteoclastogenic cytokine RANKL. We asked whether auditory ossicles are resorbed in Opg(-/-) mice, and whether these mice suffer from impaired auditory function. All three ossicles in Opg(-/-) mice showed thinning, especially at the malleal manubrium and incus body. Most notably, unlike in the case in wild-type mice, the junction between the stapes and the otic capsule was fixed in Opg(-/-) mice, and the stapedial footplate was thinner and broader. Radiological analyses revealed that malleal cortical thickness was positively correlated with tibial bone mineral density in Opg(-/-) and control littermate mice. Furthermore, progressive hearing loss was detected in Opg(-/-) mice starting at 6 to 15 weeks of age. These data suggest that osteoprotegerin plays a crucial role in hearing by protecting the auditory ossicles and otic capsule from osteoclastic bone resorption. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:414 / 419
页数:6
相关论文
共 37 条
  • [1] Adams P F, 1992, Vital Health Stat 10, P1
  • [2] Defective bone remodelling in osteoprotegerin-deficient mice
    Amizuka, N
    Shimomura, J
    Li, MQ
    Seki, Y
    Oda, M
    Henderson, JE
    Mizuno, A
    Ozawa, H
    Maeda, T
    [J]. JOURNAL OF ELECTRON MICROSCOPY, 2003, 52 (06): : 503 - 513
  • [3] Associations of serum osteoprotegerin levels with diabetes, stroke, bone density, fractures, and mortality in elderly women
    Browner, WS
    Lui, LY
    Cummings, SR
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (02) : 631 - 637
  • [4] osteoprotegerin-deficient mice develop early onset osteoporosis and arterial calcification
    Bucay, N
    Sarosi, I
    Dunstan, CR
    Morony, S
    Tarpley, J
    Capparelli, C
    Scully, S
    Tan, HL
    Xu, WL
    Lacey, DL
    Boyle, WJ
    Simonet, WS
    [J]. GENES & DEVELOPMENT, 1998, 12 (09) : 1260 - 1268
  • [5] Idiopathic hyperphosphatasia and TNFRSF11B mutations:: Relationships between phenotype and genotype
    Chong, B
    Hegde, M
    Fawkner, M
    Simonet, S
    Cassinelli, H
    Coker, M
    Kanis, J
    Seidel, J
    Tau, C
    Tüysüz, B
    Yüksel, B
    Love, D
    Cundy, T
    [J]. JOURNAL OF BONE AND MINERAL RESEARCH, 2003, 18 (12) : 2095 - 2104
  • [6] Clark Kathleen, 1995, Annals of Epidemiology, V5, P8, DOI 10.1016/1047-2797(94)00035-R
  • [7] COOPER C, 2003, EPIDEMIOLOGY OSTEOPO, P307
  • [8] A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype
    Cundy, T
    Hegde, M
    Naot, D
    Chong, B
    King, A
    Wallace, R
    Love, DR
    Seidel, J
    Fawkner, M
    Banovic, T
    Callon, KE
    Grey, AB
    Reid, IR
    Middleton-Hardie, CA
    Cornish, J
    [J]. HUMAN MOLECULAR GENETICS, 2002, 11 (18) : 2119 - 2127
  • [9] Brief report: Recombinant osteoprotegerin for juvenile Paget's disease
    Cundy, T
    Davidson, J
    Rutland, MD
    Stewart, C
    DePaoli, AM
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (09) : 918 - 923
  • [10] Requirement for NF-κB in osteoclast and B-cell development
    Franzoso, G
    Carlson, L
    Xing, LP
    Poljak, L
    Shores, EW
    Brown, KD
    Leonardi, A
    Tran, T
    Boyce, BF
    Siebenlist, U
    [J]. GENES & DEVELOPMENT, 1997, 11 (24) : 3482 - 3496