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Sensory transduction at the frog semicircular canal: how hair cell membrane potential controls junctional transmission
At the frog semicircular canals, the afferent fibers display high spontaneous activity (mEPSPs), due to transmitter release from hair cells. mEPSP and spike frequencies are modulated by stimulation that activates the hair cell receptor conductance. The relation between receptor current and transmitt...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4477162/ https://www.ncbi.nlm.nih.gov/pubmed/26157360 http://dx.doi.org/10.3389/fncel.2015.00235 |
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author | Martini, Marta Canella, Rita Rubbini, Gemma Fesce, Riccardo Rossi, Maria Lisa |
author_facet | Martini, Marta Canella, Rita Rubbini, Gemma Fesce, Riccardo Rossi, Maria Lisa |
author_sort | Martini, Marta |
collection | PubMed |
description | At the frog semicircular canals, the afferent fibers display high spontaneous activity (mEPSPs), due to transmitter release from hair cells. mEPSP and spike frequencies are modulated by stimulation that activates the hair cell receptor conductance. The relation between receptor current and transmitter release cannot be studied at the intact semicircular canal. To circumvent the problem, we combined patch-clamp recordings at the isolated hair cell and electrophysiological recordings at the cytoneural junction in the intact preparation. At isolated hair cells, the K channel blocker tetraethylammonium (TEA) is shown to block a fraction of total voltage-dependent K-conductance (IKD) that depends on TEA concentration but not on membrane potential (V(m)). Considering the bioelectric properties of the hair cell, as previously characterized by this lab, a fixed fractional block of IKD is shown to induce a relatively fixed shift in V(m), provided it lies in the range −30 to −10 mV. The same concentrations of TEA were applied to the intact labyrinth while recording from single afferent fibers of the posterior canal, at rest and during mechanical stimulation. At the peak of stimulation, TEA produced increases in mEPSP rate that were linearly related to the shifts produced by the same TEA concentrations (0.1–3 mM) in hair cell V(m) (0.7–5 mV), with a slope of 29.8 Hz/mV. The membrane potential of the hair cell is not linearly related to receptor conductance, so that the slope of quantal release vs. receptor conductance depends on the prevailing V(m) (19.8 Hz/nS at −20 mV; 11 Hz/nS at −10 mV). Changes in mEPSP peak size were negligible at rest as well as during stimulation. Since ample spatial summation of mEPSPs occurs at the afferent terminal and threshold-governed spike firing is intrinsically nonlinear, the observed increases in mEPSP frequency, though not very large, may suffice to trigger afferent spike discharge. |
format | Online Article Text |
id | pubmed-4477162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-44771622015-07-08 Sensory transduction at the frog semicircular canal: how hair cell membrane potential controls junctional transmission Martini, Marta Canella, Rita Rubbini, Gemma Fesce, Riccardo Rossi, Maria Lisa Front Cell Neurosci Neuroscience At the frog semicircular canals, the afferent fibers display high spontaneous activity (mEPSPs), due to transmitter release from hair cells. mEPSP and spike frequencies are modulated by stimulation that activates the hair cell receptor conductance. The relation between receptor current and transmitter release cannot be studied at the intact semicircular canal. To circumvent the problem, we combined patch-clamp recordings at the isolated hair cell and electrophysiological recordings at the cytoneural junction in the intact preparation. At isolated hair cells, the K channel blocker tetraethylammonium (TEA) is shown to block a fraction of total voltage-dependent K-conductance (IKD) that depends on TEA concentration but not on membrane potential (V(m)). Considering the bioelectric properties of the hair cell, as previously characterized by this lab, a fixed fractional block of IKD is shown to induce a relatively fixed shift in V(m), provided it lies in the range −30 to −10 mV. The same concentrations of TEA were applied to the intact labyrinth while recording from single afferent fibers of the posterior canal, at rest and during mechanical stimulation. At the peak of stimulation, TEA produced increases in mEPSP rate that were linearly related to the shifts produced by the same TEA concentrations (0.1–3 mM) in hair cell V(m) (0.7–5 mV), with a slope of 29.8 Hz/mV. The membrane potential of the hair cell is not linearly related to receptor conductance, so that the slope of quantal release vs. receptor conductance depends on the prevailing V(m) (19.8 Hz/nS at −20 mV; 11 Hz/nS at −10 mV). Changes in mEPSP peak size were negligible at rest as well as during stimulation. Since ample spatial summation of mEPSPs occurs at the afferent terminal and threshold-governed spike firing is intrinsically nonlinear, the observed increases in mEPSP frequency, though not very large, may suffice to trigger afferent spike discharge. Frontiers Media S.A. 2015-06-23 /pmc/articles/PMC4477162/ /pubmed/26157360 http://dx.doi.org/10.3389/fncel.2015.00235 Text en Copyright © 2015 Martini, Canella, Rubbini, Fesce and Rossi. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Martini, Marta Canella, Rita Rubbini, Gemma Fesce, Riccardo Rossi, Maria Lisa Sensory transduction at the frog semicircular canal: how hair cell membrane potential controls junctional transmission |
title | Sensory transduction at the frog semicircular canal: how hair cell membrane potential controls junctional transmission |
title_full | Sensory transduction at the frog semicircular canal: how hair cell membrane potential controls junctional transmission |
title_fullStr | Sensory transduction at the frog semicircular canal: how hair cell membrane potential controls junctional transmission |
title_full_unstemmed | Sensory transduction at the frog semicircular canal: how hair cell membrane potential controls junctional transmission |
title_short | Sensory transduction at the frog semicircular canal: how hair cell membrane potential controls junctional transmission |
title_sort | sensory transduction at the frog semicircular canal: how hair cell membrane potential controls junctional transmission |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4477162/ https://www.ncbi.nlm.nih.gov/pubmed/26157360 http://dx.doi.org/10.3389/fncel.2015.00235 |
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