Human otosclerotic bone-derived peptide decreases the gain of the electromotility in isolated outer hair cells

Hearing Research

Volumn 95, Issue 1-2, 1996, Pages 100-107

  Sziklai, Istvan ^a,b  

^a SEMMELWEIS UNIVERSITY OF MEDICINE   (Hungary)

^b NORTHWESTERN UNIVERSITY   (United States)

Author keywords

Acetylcholine; Caffeine; Electromotility; Otosclerosis; Outer hair cell; Sensorineural hearing loss

Indexed keywords

ACETYLCHOLINE; CAFFEINE; CALCIUM ION; PEPTIDE;

ANIMAL CELL; ARTICLE; BASOLATERAL MEMBRANE; CALCIUM CELL LEVEL; CELL MOTILITY; COCHLEA; CONDUCTION DEAFNESS; GUINEA PIG; HAIR CELL; HUMAN; HUMAN TISSUE; ISOTACHOPHORESIS; NONHUMAN; OTOSCLEROSIS; PERCEPTION DEAFNESS; PERILYMPH; PRIORITY JOURNAL; PROTEIN ISOLATION;

EID: 0029974231     PISSN: 03785955     EISSN: None     Source Type: Journal    
DOI: 10.1016/0378-5955(96)00027-5     Document Type: Article

References (41)

1. Ashmore, J.F. (1987) A fast motile response in guinea pig outer hair cells: the cellular basis of the cochlear amplifier. J. Physiol. (Lond.) 388, 323-347.
2. Brownell, W.E. (1990) Outer hair cell electromotility and otoacoustic emissions. Ear Hear. 11, 82-92.
3. Brownell, W.E., Bader, C.R., Bertrand, D. and Ribaupierre, Y. (1985) Evoked mechanical responses of isolated cochlear hair cells. Science 227, 194-196.
4. Causse, J., Chevance, L.G., Bretlau, P., Jörgensen, M.B., Uriel, J. and Berges, J. (1977) Enzymatic concept of otospongiosis and cochlear otospongiosis. Clin. Otolar. 2, 23-32.
5. Causse, J., Uriel, J., Berges, J., Bretlau, P., Shambaugh, G.E. and Causse, J.B. (1985) Objective changes in trypsin, alpha-1-antitrypsin and alpha-2-macroglobuline values as a result of sodium fluoride treatment in patients with otosclerosis. Am. J. Otol. 6, 38-42.
6. Chevance, L.G., Causse, J. and Berges, J. (1973) Données récents sur la biochimie de l'otospongiose. Les protéases des fluides labyrinthiques au cours de l'otospongiose. Can. J. Otol. 2, 124-132.
7. Clark, B.A., Hallworth, R. and Evans, B.N. (1990) Calibration of photodiode measurements of cell motion by a transmission optical lever method. Pflügers Arch. 415, 490-493.
8. Dallos, P. (1988) Cochlear neurobiology: Some key experiments and concepts of the past two decades. In: G.M. Edelman, E.W. Gall and W.M. Cowan (Eds.), Functions of the Auditory System. J. Wiley, New York, pp. 153-188.
9. 2+ concentration and hyperpolarizes the guinea pig outer hair cell. Hear. Res. 67, 179-188.
10. Dorsey, T.E., McDonald, P.W. and Roels, O.A. (1977) A heated biuret-Folin protein assay which gives equal absorbence with different proteins. Anal. Biochem. 78, 156-164.
11. Evans, B.N., Hallworth, R. and Dallos, P. (1991) Outer hair cell electromotility: the sensitivity and vulnerability of the DC component. Hear. Res. 52, 288-304.
12. Flock, A., Flock, B. and Ulfendahl, M. (1986) Mechanisms and movement in outer hair cells and a possible structural basis. Arch. Otorhinolaryngol. 243, 83-90.
13. Fuchs, P.A. and Murrow, B.W. (1992a) A novel cholinergic receptor mediates inhibition of chick cochlear hair cells. Proc. R. Soc. Lond. B 248, 35-40.
14. Fuchs, P.A. and Murrow, B.W. (1992b) Cholinergic inhibition of short (outer) hair cells of the chick's cochlea. J. Neurosci. 12, 800-809.
15. Housley, G.D. and Ashmore, J.F. (1992) Ionic currents of outer hair cells isolated from the guinea pig cochlea. J. Physiol. (Lond.) 448, 73-98.
16. Kachar, B., Brownell, W.E., Altschuler, R. and Fex, J. (1986) Electrokinetic shape changes of cochlear outer hair cells. Nature 322, 365-368.
17. Kelemen, G. and Linthicum, F.H. (1969) Labyrinthine otosclerosis. Acta Otolaryngol. (Stockh.) 253, (Suppl.) 5-65.
18. Kelemen, G. and Alonso, A. (1980) Penetration of the cochlear endost by the fibrous component of the otosclerotic focus. Acta Otolaryngol. (Stockh.) 89, 453-458.
19. Klinke, R. (1986) Neurotransmission in the inner ear. Hear. Res. 22, 235-243.
20. Lawrence, M. (1966) Possible influence of cochlear otosclerosis on inner ear fluids. Ann. Otol. 75, 553-558.
21. Ribari, O. and Sziklai, I. (1983) Examination of noncollagen protein composition of the footplate and superstructure of the otosclerotic stapes. Acta Otolaryngol. (Stockh.) 95, 580-584.
22. Ribari, O., Sziklai, I., Kiss, J.G. and Sohar, I. (1983) Cathepsin B activity in otosclerosis. Arch. Otorhinolaryngol. 238, 123-125
23. Ribari, O., Sziklai, I. and Kiss, J.G. (1987) Proteolytic enzymes in otosclerosis. Significance of proteolytic enzymes in otosclerotic bone remodelling. ORL (Basel) 49, 282-286.
24. Ribari, O. and Sziklai, I. (1988) Cathepsin D activity in otosclerotic bone and perilymph. Acta Otolaryngol. (Stockh.) 105, 549-552.
25. Rossi, G. and Olina, M. (1989) Otosclerosis. An osteodystrophy solely located in the osseous labyrinth with an inconstant clinical picture. In: R. Filipo (Ed.), Otosclerosis. Kugler and Ghedini Publ., Amsterdam, pp. 37-42.
26. Rüedi, L. (1965) Histopathologic confirmation of labyrinthine otosclerosis. Laryngoscope 75, 1582-1609.
27. Santos-Sacchi, J. (1989) Asymmetry in voltage-dependent movements of isolated outer hair cells from the organ of Corti. J. Neurosci. 9, 2954-2962.
28. Santos-Sacchi, J. (1992) On the frequency limit and phase of outer hair cell motility: effects of the membrane filter. J. Neurosci. 12, 1906-1916.
29. Santos-Sacchi, J. and Dilger, D.P. (1988) Whole cell currents and mechanical responses of isolated outer hair cells. Hear. Res. 35, 143-150.
30. Schindler, O., Schnieder, E.A. and Wullstein, H.L. (1965) Verleichende Bestimmung einiger Electrolyte und organische Substanzen in der Perilymph otosklerosekranker Patienten. Acta Otolaryngol. (Stockh.) 19, 309-319.
31. Siebenmann, F. (1899) Multiple Spongiosierung der Labyrinthkapsel als sections befund bei einem Fall von Progressiever Schwerhörigkeit. Z. Ohrenheilk. 34, 356-374.
32. Slepecky, N., Ulfendahl, M. and Flock, A. (1988) Effects of Caffeine and tetracaine on outer hair cell shortening suggest intracellular calc ium involvement. Hear. Res. 32, 11-22.
33. Sziklai, I. and Dallos, P. (1993) Acetylcholine controls the gain of the voltage-to-movement converter in isolated outer hair cells. Acta Otolaryngol. (Stockh.) 113, 326-329.
34. Sziklai, I., He, Z.Z. and Dallos, P. (1996) Effect of acetylcholine and GABA on the transfer function of electromotility in isolated OHCs, submitted.
35. Sziklai, I., Grof, J., Ribari, O., Menyhart, J. and Piffko, P. (1985a) Peptides of the otosclerotic perilymph examined by analytical isotachophoresis. Acta Otolaryngol. (Stockh.) 99, 25-34.
36. Sziklai, I., Grof, J., Ribari, O. and Menyhart, J. (1985b) Possible role of peptides derived from otosclerotic bone in the mechanism of sensorineural hearing loss. Acta Otolaryngol. (Stockh.) 100, 253-259.
37. Sziklai, I., Kiss, J.G. and Ribari, O. (1986) Inhibition of myosin light-chain kinase activity in the organ of Corti by 0.3-5 kD substances of the otosclerotic perilymph. Arch. Otorhinolaryngol. 243, 229-232.
38. Wullstein, H.L., Kley, W., Rauch, S. and Köstlin, A. (1960) Zur Biochemie der Perilymph operierter Otosklerosen. Z. Laryngol. Otol. 39, 665-672.
39. Zenner, H.P. (1986) Motile responses in outer hair cells. Hear. Res. 22, 83-90.
40. Zenner, H.P., Zimmermann, U., and Schmitt, U. (1985) Reversible contraction of isolated mammalian cochlear outer hair cells. Hear. Res. 18, 127-133.
41. Zenner, H.P., Zimmermann, U. and Gitter, A.H. (1987) Fast motility of isolated mammalian auditory sensory cells. Biochim. Biophys. Res. Comm. 149, 304-308.