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Publication : Activation of BK and SK channels by efferent synapses on outer hair cells in high-frequency regions of the rodent cochlea.

First Author  Rohmann KN Year  2015
Journal  J Neurosci Volume  35
Issue  5 Pages  1821-30
PubMed ID  25653344 Mgi Jnum  J:218972
Mgi Id  MGI:5619208 Doi  10.1523/JNEUROSCI.2790-14.2015
Citation  Rohmann KN, et al. (2015) Activation of BK and SK channels by efferent synapses on outer hair cells in high-frequency regions of the rodent cochlea. J Neurosci 35(5):1821-30
abstractText  Cholinergic neurons of the brainstem olivary complex project to and inhibit outer hair cells (OHCs), refining acoustic sensitivity of the mammalian cochlea. In all vertebrate hair cells studied to date, cholinergic inhibition results from the combined action of ionotropic acetylcholine receptors and associated calcium-activated potassium channels. Although inhibition was thought to involve exclusively small conductance (SK potassium channels), recent findings have shown that BK channels also contribute to inhibition in basal, high-frequency OHCs after the onset of hearing. Here we show that the waveform of randomly timed IPSCs (evoked by high extracellular potassium) in high-frequency OHCs is altered by blockade of either SK or BK channels, with BK channels supporting faster synaptic waveforms and SK channels supporting slower synaptic waveforms. Consistent with these findings, IPSCs recorded from high-frequency OHCs that express BK channels are briefer than IPSCs recorded from low-frequency (apical) OHCs that do not express BK channels and from immature high-frequency OHCs before the developmental onset of BK channel expression. Likewise, OHCs of BKalpha(-/-) mice lacking the pore-forming alpha-subunit of BK channels have longer IPSCs than do the OHCs of BKalpha(+/+) littermates. Furthermore, serial reconstruction of electron micrographs showed that postsynaptic cisterns of BKalpha(-/-) OHCs were smaller than those of BKalpha(+/+) OHCs, and immunofluorescent quantification showed that efferent presynaptic terminals of BKalpha(-/-) OHCs were smaller than those of BKalpha(+/+) OHCs. Together, these findings indicate that BK channels contribute to postsynaptic function, and influence the structural maturation of efferent-OHC synapses.
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