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Modeling Hair Cell Tuning by Expression Gradients of Potassium Channel Beta Subunits

Overview
Journal Biophys J
Publisher Cell Press
Specialty Biophysics
Date 2001 Dec 26
PMID 11751296
Citations 16
Authors
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Abstract

The receptor potential of sensory hair cells arises from the gating of mechanosensitive cation channels, but its amplitude and time course also depend on the number and kinetics of voltage-gated ion channels in each cell. Prominent among these are "BK" potassium channels encoded by the slo gene that support electrical tuning in some hair cells. Hair cells tuned to low frequencies have slowly gating BK channels, whereas those of higher-frequency hair cells gate more rapidly. Alternative splicing of the slo gene mRNA that encodes the pore-forming alpha subunit can alter BK channel kinetics, and gating is dramatically slowed by coexpression with modulatory beta subunits. The effect of the beta subunit is consistent with low-frequency tuning, and beta mRNA is expressed at highest levels in the low frequency apex of the bird's auditory epithelium. How might an expression gradient of beta subunits contribute to hair cell tuning? The present work uses a computational model of hair cell-tuning based on the functional properties of BK channels expressed from hair cell alpha and beta slo cDNA. The model reveals that a limited tonotopic gradient could be achieved simply by altering the fraction of BK channels in each hair cell that are combined with beta subunits. However, complete coverage of the tuning spectrum requires kinetic variants in addition to those modeled here.

Citing Articles

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References
1.
Barrett J, Magleby K, Pallotta B . Properties of single calcium-activated potassium channels in cultured rat muscle. J Physiol. 1982; 331:211-30. PMC: 1197747. DOI: 10.1113/jphysiol.1982.sp014370. View

2.
Uebele V, LAGRUTTA A, Wade T, Figueroa D, Liu Y, McKenna E . Cloning and functional expression of two families of beta-subunits of the large conductance calcium-activated K+ channel. J Biol Chem. 2000; 275(30):23211-8. DOI: 10.1074/jbc.M910187199. View

3.
Lewis R, Hudspeth A . Voltage- and ion-dependent conductances in solitary vertebrate hair cells. Nature. 1983; 304(5926):538-41. DOI: 10.1038/304538a0. View

4.
Art J, Fettiplace R . Variation of membrane properties in hair cells isolated from the turtle cochlea. J Physiol. 1987; 385:207-42. PMC: 1192345. DOI: 10.1113/jphysiol.1987.sp016492. View

5.
Hudspeth A, Lewis R . Kinetic analysis of voltage- and ion-dependent conductances in saccular hair cells of the bull-frog, Rana catesbeiana. J Physiol. 1988; 400:237-74. PMC: 1191806. DOI: 10.1113/jphysiol.1988.sp017119. View