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Comparison of Cochlear Morphology and Apoptosis in Mouse Models of Presbycusis

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Objectives. Morphological studies on presbycusis, or age-related hearing loss, have been performed in several different strains of mice that demonstrate hearing loss with auditory pathology. The C57BL/6 (C57) mouse is a known model of early onset presbycusis, while the CBA mouse is characterized by relatively late onset hearing loss. We performed this study to further understand how early onset hearing loss is related with the aging process of the cochlea. Methods. We compared C57 cochlear pathology and its accompanying apoptotic processes to those in CBA mice. Hearing thresholds and outer hair cell functions have been evaluated by auditory brainstem response (ABR) recordings and distortion product otoacoustic emission (DPOAE). Results. ABR recordings and DPOAE studies demonstrated high frequency hearing loss in C57 mice at P3mo of age. Cochlear morphologic studies of P1mo C57 and CBA mice did not show differences in the organ of Corti, spiral ganglion, or stria vascularis. However, from P3mo and onwards, a predominant early outer hair cell degeneration at the basal turn of the cochlea in C57 mice without definitive degeneration of spiral ganglion cells and stria vascularis/spiral ligament, compared with CBA mice, was observed. Additionally, apoptotic processes in the C57 mice also demonstrated an earlier progression. Conclusion. These data suggest that the C57 mouse could be an excellent animal model for early onset ‘sensory’ presbycusis in their young age until P6mo. Further studies to investigate the intrinsic or extrinsic etiologic factors that lead to the early degeneration of organ of Corti, especially in the high frequency region, in C57 mice may provide a possible pathological mechanism of early onset hearing loss.

Abstract

Objectives. Morphological studies on presbycusis, or age-related hearing loss, have been performed in several different strains of mice that demonstrate hearing loss with auditory pathology. The C57BL/6 (C57) mouse is a known model of early onset presbycusis, while the CBA mouse is characterized by relatively late onset hearing loss. We performed this study to further understand how early onset hearing loss is related with the aging process of the cochlea. Methods. We compared C57 cochlear pathology and its accompanying apoptotic processes to those in CBA mice. Hearing thresholds and outer hair cell functions have been evaluated by auditory brainstem response (ABR) recordings and distortion product otoacoustic emission (DPOAE). Results. ABR recordings and DPOAE studies demonstrated high frequency hearing loss in C57 mice at P3mo of age. Cochlear morphologic studies of P1mo C57 and CBA mice did not show differences in the organ of Corti, spiral ganglion, or stria vascularis. However, from P3mo and onwards, a predominant early outer hair cell degeneration at the basal turn of the cochlea in C57 mice without definitive degeneration of spiral ganglion cells and stria vascularis/spiral ligament, compared with CBA mice, was observed. Additionally, apoptotic processes in the C57 mice also demonstrated an earlier progression. Conclusion. These data suggest that the C57 mouse could be an excellent animal model for early onset ‘sensory’ presbycusis in their young age until P6mo. Further studies to investigate the intrinsic or extrinsic etiologic factors that lead to the early degeneration of organ of Corti, especially in the high frequency region, in C57 mice may provide a possible pathological mechanism of early onset hearing loss.

참고문헌 (21)

  1. Kocher W, "Research on the genetics and pathology of the development of delayed hereditary deafness in the mouse (Mus musculus)", Arch Ohren Nasen Kehlkopfheilkd, 177, pp.108~145 (1960)
  2. Johnson KR, "A major gene affecting age-related hearing loss in C57BL", 6J mice, 1997, pp.114(1-2), 83~92
  3. Siemens J, "Cadherin 23 is a component of the tip link in hair-cell stereocilia", Nature, 428(6986), pp.950~955 (2004)
  4. Spongr VP, "Quantitative measures of hair cell loss in CBA and C57BL", 6 mice throughout their life spans, 1997, pp.101(6), 3546~3553
  5. Ichimiya I, "Age-related changes in the murine cochlear lateral wall", Hear Res, 139(1-2), pp.116~122 (2000)
  6. Li HS, "Age-related degeneration of the organ of Corti in two genotypes of mice", ORL J Otorhinolaryngol Relat Spec, 56(2), pp.61~67 (1994)
  7. Schuknecht HF, "Cochlear pathology in presbycusis", Ann Otol Rhinol Laryngol, 102(1 Pt 2), pp.1~16 (1993)
  8. Li HS, "Age-related loss of auditory sensitivity in two mouse genotypes", Acta Otolaryngol, 111(5), pp.827~834 (1991)
  9. Bronson RT, "Rate of occurrence of lesions in 20 inbred and hybrid genotypes of rats and mice sacrificed at 6 month intervals during the first years of life. In: Genetic effects on aging II", pp.279~357 (1990), Telford Press
  10. Sha SH, "Age-related auditory pathology in the CBA", J mouse, 2008, pp.243(1-2), 87~94
  11. Youle RJ, "The BCL-2 protein family: opposing activities that mediate cell death", Nat Rev Mol Cell Biol, 9(1), pp.47~59 (2008)
  12. McFadden SL, "Cu", Zn SOD deficiency potentiates hearing loss and cochlear pathology in aged 129,CD-1 mice, 1999, pp.413(1), 101~112
  13. McFadden SL, "Age-related cochlear hair cell loss is enhanced in mice lacking copper", zinc superoxide dismutase, 1999, pp.20(1), 1~8
  14. Sha SH, "Activation of cell death pathways in the inner ear of the aging CBA", J mouse, 2009, pp.254(1-2), 92~99
  15. Someya S, "Agerelated hearing loss in C57BL", 6J mice is mediated by Bak-dependent mitochondrial apoptosis, 2009, pp.106(46), 19432~19437
  16. Ohlemiller KK, "Divergence of hearing sensitivity and endocochlear potential (EP) in CBA", J and CBA, Assoc Res Otolaryngol, pp.2007, ~
  17. Hultcrantz M, "Inner ear morphology in CBA", Ca and C57BL, Eur Arch Otorhinolaryngol, pp.1993, 250(5)[DOI]
  18. Anderson SD, "The evoked cochlear mechanical response in laboratory primates: a preliminary report", Arch Otorhinolaryngol, 224(1-2), pp.47~54 (1979)
  19. Brownell WE, "Outer hair cell electromotility and otoacoustic emissions", Ear Hear, 11(2), pp.82~92 (1990)
  20. Willott JF, "Genetics of age-related hearing loss in mice: IV. cochlear pathology and hearing loss in 25 BXD recombinant inbred mouse strains", Hear Res., 119(1-2), pp.27~36 (1998)
  21. Tadros SF, "Apoptosis-related genes change their expression with age and hearing loss in the mouse cochlea", Apoptosis, 13(11), pp.1303~1321 (2008)

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