Evidence for a medial K+ recycling pathway from inner hair cells

Hearing Research

Volumn 118, Issue 1-2, 1998, Pages 1-12

  Spicer, Samuel S ^a   Schulte, Bradley A ^a  

^a MEDICAL UNIVERSITY OF SOUTH CAROLINA   (United States)

Author keywords

Aging; Cochlea; Gerbil; Immunohistochemistry; Interdental cell; Ion transport; Limbus

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); POTASSIUM ION;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL TYPE; COCHLEA DUCT; FEMALE; GERBIL; HAIR CELL; INNER EAR; MALE; NONHUMAN; POTASSIUM TRANSPORT; PRIORITY JOURNAL; RECYCLING;

AGING; ANIMALS; COCHLEA; ENDOLYMPH; FEMALE; FIBROBLASTS; GAP JUNCTIONS; GERBILLINAE; HAIR CELLS, INNER; IMMUNOHISTOCHEMISTRY; ION TRANSPORT; LIMBIC SYSTEM; MALE; NA(+)-K(+)-EXCHANGING ATPASE; POTASSIUM; SPIRAL GANGLION; STROMAL CELLS; VESTIBULAR NUCLEUS, LATERAL;

EID: 0031900032     PISSN: 03785955     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-5955(98)00006-9     Document Type: Article

References (37)

1. 35 in the membranes of the inner ear of the rat. Science. 118:1953;520-521.
2. Chen H., Thalmann I., Adams J.C., Avarham K.B., Copeland N.G., Jenkins N.A., Beier D.R., Corey D.P., Thalamann R., Duyk G. cDNA cloning, tissue distribution, and chromosomal localization of Ocp2, a gene encoding a putative transcription-associated factor predominately expressed in the auditory organs. Genomics. 27:1995;389-398.
3. Duvall, A.J., Sutherland, C.R., 1970. The ultrastructure of the extrasensory cells in the cochlear duct. In: Paprella, M.M. (Ed.), Biochemical Mechanisms in Hearing and Deafness. C.C. Thomas, Springfield, IL, pp. 149-170.
4. Engström, H., Ades, H.W., 1973. The ultrastructure of the organ of Corti. In: Friedmann, I. (Ed.), The Ultrastructure of Sensory Organs. North Holland, Amsterdam, pp. 85-151.
5. Gratton, M.A., Spicer, S.S., 1996. Immunohistochemical changes in the lateral wall of the quiet-aged gerbil. Abstract, 19th Midwinter Research Meeting, Association for Research in Otolaryngology.
6. Hilding A.C. Studies on otic labyrinth; on origin and insertion of tectorial membrane. Ann. Otol. Rhinol. Laryngol. 61:1952;354-370.
7. Ilberg C.V. Electron microscopic studies on the diffusion and resorption of thorium dioxide in the cochlea of the guinea pig. 3. Limbus spiralis (German). Arch. Klin. Exp. Ohren-, Nasen-, Kehlkopfheilkd. 192:1968;163-175.
8. Ishiyama E., Weibel J., Keels E.W., Richardson T.L. Ultrastructure of the interdental cells in mammals. Pract. Oto-rhino-laryngol. 32:1970;321-334.
9. Iurato S. Submicroscopic structure of the membranous labyrinth. III. The supporting structure of Corti's organ (basilar membrane, limbus spiralis and spiral ligament). Z. Zellforsch. 56:1962;40-96.
10. Iurato S., Franke K., Luciano L., Wermbler G., Pannese E., Reale E. Intercellular junctions in the organ of Corti as revealed by freeze fracturing. Acta Otolaryngol. (Stockh.). 82:1976;57-69.
11. Kikuchi T., Kimura R.S., Paul D.L., Adams J.C. Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis. Anat. Embryol. 191:1995;101-118.
12. Kimura R.S. The ultrastructure of the organ of Corti. Int. Rev. Cytol. 42:1975;173-222.
13. Kimura, R.S., 1984. Sensory and accessory epithelia of the cochlea. In: Friedmann, I. and Ballantyne, J. (Eds.), Ultrastructural Atlas of the Inner Ear. Buttersworth, London, pp. 101-132.
14. Kimura R.S., Nye C.L., Southard R.E. Normal and pathologic features of the limbus spiralis and its functional significance. Ann. Otolaryngol. 11:1990;99-111.
15. Konishi T., Hamrick P.E., Walsh P.J. Ion transport in guinea pig cochlea. I. Potassium and sodium transport. Acta Otolaryngol. 86:1978;22-34.
16. Lim D.J. Three dimensional observation of the inner ear with the scanning electron microscope. Acta Otolaryngol. Suppl. 255:1969;1-38.
17. Lim D.J. Morphology and function of the interdental cell. J. Laryngol. 84:1970;1241-1256.
18. Marcus, D.C., 1986. Non-sensory electrophysiology of the cochlea: stria vascularis. In: Altschuler, R.A., Hoffman, D.W., Bobbin, R.P. (Eds.), Neurobiology of Hearing: The Cochlea. Raven Press, New York, pp. 123-137.
19. McGuirt J.P., Schulte B.A. distribution of immunoreactive α and β subunit isoforms of Na,K-ATPase in the gerbil inner ear. J. Histochem. Cytochem. 42:1994;843-853.
20. Mills J.H., Schmiedt R.A., Kulish L.F. Age-related changes in auditory potentials of Mongolian gerbil. Hear. Res. 46:1990;201-210.
21. Mori N., Sakagami M., Fukazawa K., Matsunaga T. An immunohistochemical and electrophysiological study on Isk protein in the stria vascularis of the guinea pig. Eur. Arch. Otorhinolaryngol. 250:1993;186-189.
22. Salt, A.N., Konishi, T., 1986. The cochlear fluids: perilymph and endolymph. In: Altschuler, R.A., Hoffman, D.W., Bobbin, R.P. (Eds.), Neurobiology of Hearing: The Cochlea. Raven Press, New York, pp. 108-122.
23. Santi, P.A., 1988. Cochlear microanatomy and ultrastructure. In: Jahn, A.F., Santos-Sacchi, J. (Eds.), Physiology of the Ear. Raven Press, New York, pp. 173-199.
24. Santos-Sacchi J., Dallos P. Intercellular communication in the supporting cells of the organ of Corti. Hear. Res. 9:1983;317-326.
25. Schmiedt R.A. Spontaneous rates, thresholds, and tuning of auditory nerve fibers: comparison between cat and gerbil. Hear. Res. 42:1989;23-36.
26. +-ATPase in the gerbil cochlea. J. Histochem. Cytochem. 37:1989;127-134.
27. d loci. Hear. Res. 78:1994;65-76.
28. sK channel in strial marginal cells. Voltage-dependence, ion-selectivity, inhibition by 293B and sensitivity to clofilium. Audit. Neurosci. 3:1997;215-230.
29. Spicer S.S., Schulte B.A. Differentiation of inner ear fibrocytes according to their ion transport related activity. Hear. Res. 56:1991;53-64.
30. Spicer S.S., Schulte B.A. Differences along the place-frequency map in the structure of supporting cells in the gerbil cochlea. Hear. Res. 79:1994;161-177.
31. Spicer S.S., Schulte B.A. Ultrastructural differentiation of the first Hensen cell in the gerbil cochlea as a distinct cell type. Anat. Rec. 240:1994;149-156.
32. Spicer S.S., Schulte B.A. The fine structure of spiral ligament cells relates to ion return to the stria and varies with place-frequency. Hear. Res. 100:1996;80-100.
33. Tarnowski B.I., Schmiedt R.A., Hellstrom L.I., Lee F.S., Adams J.C. Age-related changes in cochleas of Mongolian gerbils. Hear. Res. 54:1991;123-134.
34. Voldrich L. Morphology and function of the epithelium of the limbus spiralis cochleae. Acta Otolaryngol. 63:1967;503-514.
35. Wada J., Kambayashi J., Marcus D.C., Thalmann R. Vascular perfusion of the cochlea: effect of potassium-free and rubidium-substituted media. Arch. Otorhinolaryngol. Beg. 225:1979;79-81.
36. Yoho E.R., Thomopoulos G.N., Thalmann I., Thalmann R., Schulte B.A. Localization of organ of Corti protein II in the adult and developing gerbil cochlea. Hear. Res. 104:1997;47-56.
37. Zidanic M., Brownell W.E. Fine structure of the intracochlear potential field. I. The silent current. Biophys. J. 57:1994;1253-1268.