Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier

Nature

Volumn 419, Issue 6904, 2002, Pages 300-304

  Liberman, M Charles ^a   Gao, Jiangang ^b   He, David Z Z ^c   Wu, Xudong ^b,d   Jia, Shuping ^c   Zuo, Jian ^b  

^a MASSACHUSETTS EYE AND EAR INFIRMARY   (United States)

^b ST JUDE CHILDREN S RESEARCH HOSPITAL   (United States)

^c BOYS TOWN NATIONAL RESEARCH HOSPITAL   (United States)

^d UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMPLIFICATION; AUDITION; PROTEINS;

MAMMALS;

CELLS;

COMPLEMENTARY DNA; MEMBRANE PROTEIN; PRESTIN; UNCLASSIFIED DRUG;

AUDITORY CUE; MAMMAL; PROTEIN; SENSITIVITY ANALYSIS;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CELL MOTILITY; COCHLEA; DNA SEQUENCE; EMBRYO; FEMALE; GENE MUTATION; GENOTYPE; HAIR CELL; INNER EAR; MALE; MOUSE; NONHUMAN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SIGNAL TRANSDUCTION;

ANIMALS; COCHLEA; ELECTROPHYSIOLOGY; GENE DELETION; GENOTYPE; HAIR CELLS, OUTER; HEARING; IMMUNOHISTOCHEMISTRY; MICE; PHENOTYPE; PROTEINS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION;

ANIMALIA; MAMMALIA;

EID: 0037136582     PISSN: 00280836     EISSN: None     Source Type: Journal    
DOI: 10.1038/nature01059     Document Type: Article

References (29)

1. Gold, T. Hearing. II. The physical basis of the action of the cochlea. Proc. R. Soc. Lond. B 135, 492-498 (1948).
2. Dallos, P. & Harris, D. Properties of auditory nerve responses in absence of outer hair cells. J. Neurophysiol. 41, 365-383 (1978).
3. Brown, M. C., Nuttall, A. L. & Masta, R. I. Intracellular recordings from cochlear inner hair cells: effects of stimulation of the crossed olivocochlear efferents. Science 222, 69-72 (1983).
4. Dallos, P. The active cochlea. J. Neurosci. 12, 4575-4585 (1992).
5. Brownell, W. E., Bader, C. R., Bertrand, D. & de Ribaupierre, Y. Evoked mechanical responses of isolated cochlear outer hair cells. Science 227, 194-196 (1985).
6. Kachar, B., Brownell, W. E., Altschuler, R. & Fex, J. Etectrokinetic shape changes of cochlear outer hair cells. Nature 322, 365-368 (1986).
7. Ashmore, J. F. A fast motile response in guinea-pig outer hair cells: The cellular basis of the cochlear amplifier. J. Physiol. 388, 323-347 (1987).
8. Ashmore, J. F. Cochlear Mechanisms (eds Wilson, J. P. & Kemp, D. T.) 107-116 (Plenum, London, 1989).
9. Santos-Sacchi, J. Reversible inhibition of voltage-dependent outer hair cell motility and capacitance. J. Neurosci. 11, 3096-3110 (1991).
10. Zheng, J. et al. Prestin is the motor protein of cochlear outer hair cells. Nature 405, 149-155 (2000).
11. Belyantseva, I. A., Adler, H. J., Curi, R., Frolenkov, G. I. & Kachar, B. Expression and localization of prestin and the sugar transporter GLUT-5 during development of electromotility in cochlear outer hair cells. J. Neurosci. 20, RC116 (2000).
12. Oliver, D. et al. Intracellular anions as the voltage sensor of prestin, the outer hair cell motor protein. Science 292, 2340-2343 (2001).
13. Forge, A. Structural features of the lateral walls in mammalian cochlear outer hair cells. Cell Tissue Res. 265, 473-483 (1991).
14. Dallos, P. & Fakler, B. Prestin, a new type of motor protein. Nature Rev. Mol. Cell Biol. 3, 104-111 (2002).
15. Bohne, B. A. & Rabbitt, K. D. Holes in the reticular lamina after noise exposure: implication for continuing damage in the organ of Corti. Hear. Res. 11, 41-53 (1983).
16. Holt, J. R. et al. A chemical-genetic strategy implicates myosin-1c in adaptation by hair cells. Cell 108, 371-381 (2002).
17. Kros, C. J. et al. Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutations. Nature Neurosci. 5, 41-47 (2002).
18. Dallos, P. & Wang, C. Y. Bioelectric correlates of kanamycin intoxication. Audiology 13, 277-289 (1974).
19. Kemp, D. T. Stimulated acoustic emissions from within the human auditory system. J. Acoust. Soc. Am. 64, 1386-1391 (1978).
20. Johnstone, B. M., Patuzzi, R. & Yates, G. K. Basilar membrane measurements and the travelling wave. Hear. Res. 22, 147-153 (1986).
21. Ruggero, M. A. & Rich, N. C. Application of a commercially-manufactured Doppler-shift laser velocimeter to the measurement of basilar-membrane vibration. Hear. Res. 51, 215-230 (1991).
22. Sellick, P. M., Patuzzi, R. & Johnstone, B. M. Measurement of basilar membrane motion in the guinea pig using the Mossbauer technique. J. Acoust. Soc. Am. 72, 131-141 (1982).
23. Kiang, N. Y. & Moxon, E. C. Tails of tuning curves of auditory-nerve fibers. J. Acoust. Soc. Am. 55, 620-630 (1974).
24. Ruggero, M. A. Responses to sound of the basilar membrane of the mammalian cochlea. Curr. Opin. Neurobiol. 2, 449-456 (1992).
25. Manley, G. A. Cochlear mechanisms from a phylogenetic viewpoint. Proc. Natl Acad. Sci. USA 97, 11736-11743 (2000).
26. Fettiplace, R., Ricci, A. J. & Hackney, C. M. Clues to the cochlear amplifier from the turtle ear. Trends Neurosci. 24, 169-175 (2001).
27. Hudspeth, A. J. Mechanical amplification of stimuli by hair cells. Curr. Opin. Neurobiol. 7, 480-486 (1997).
28. Ehret, G. The Auditory Psychobiology of the Mouse (ed. Willott, J. F.)) 169-200 (Charles Thomas, Springfield, Illinois, 1983).
29. He, D. Z., Evans, B. N. & Dallos, P. First appearance and development of electromotility in neonatal gerbil outer hair cells. Hear. Res. 78, 77-90 (1994).