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Fine Tuning of Ca(V)1.3 Ca(2+) Channel Properties in Adult Inner Hair Cells Positioned in the Most Sensitive Region of the Gerbil Cochlea
Hearing relies on faithful signal transmission by cochlear inner hair cells (IHCs) onto auditory fibres over a wide frequency and intensity range. Exocytosis at IHC ribbon synapses is triggered by Ca(2+) inflow through Ca(V)1.3 (L-type) Ca(2+) channels. We investigated the macroscopic (whole-cell) a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237458/ https://www.ncbi.nlm.nih.gov/pubmed/25409445 http://dx.doi.org/10.1371/journal.pone.0113750 |
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author | Zampini, Valeria Johnson, Stuart L. Franz, Christoph Knipper, Marlies Holley, Matthew C. Magistretti, Jacopo Russo, Giancarlo Marcotti, Walter Masetto, Sergio |
author_facet | Zampini, Valeria Johnson, Stuart L. Franz, Christoph Knipper, Marlies Holley, Matthew C. Magistretti, Jacopo Russo, Giancarlo Marcotti, Walter Masetto, Sergio |
author_sort | Zampini, Valeria |
collection | PubMed |
description | Hearing relies on faithful signal transmission by cochlear inner hair cells (IHCs) onto auditory fibres over a wide frequency and intensity range. Exocytosis at IHC ribbon synapses is triggered by Ca(2+) inflow through Ca(V)1.3 (L-type) Ca(2+) channels. We investigated the macroscopic (whole-cell) and elementary (cell-attached) properties of Ca(2+) currents in IHCs positioned at the middle turn (frequency ∼2 kHz) of the adult gerbil cochlea, which is their most sensitive hearing region. Using near physiological recordings conditions (body temperature and a Na(+) based extracellular solution), we found that the macroscopic Ca(2+) current activates and deactivates very rapidly (time constant below 1 ms) and inactivates slowly and only partially. Single-channel recordings showed an elementary conductance of 15 pS, a sub-ms latency to first opening, and a very low steady-state open probability (P (o): 0.024 in response to 500-ms depolarizing steps at ∼−18 mV). The value of P (o) was significantly larger (0.06) in the first 40 ms of membrane depolarization, which corresponds to the time when most Ca(2+) channel openings occurred clustered in bursts (mean burst duration: 19 ms). Both the P (o) and the mean burst duration were smaller than those previously reported in high-frequency basal IHCs. Finally, we found that middle turn IHCs are likely to express about 4 times more Ca(2+) channels per ribbon than basal cells. We propose that middle-turn IHCs finely-tune Ca(V)1.3 Ca(2+) channel gating in order to provide reliable information upon timing and intensity of lower-frequency sounds. |
format | Online Article Text |
id | pubmed-4237458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-42374582014-11-21 Fine Tuning of Ca(V)1.3 Ca(2+) Channel Properties in Adult Inner Hair Cells Positioned in the Most Sensitive Region of the Gerbil Cochlea Zampini, Valeria Johnson, Stuart L. Franz, Christoph Knipper, Marlies Holley, Matthew C. Magistretti, Jacopo Russo, Giancarlo Marcotti, Walter Masetto, Sergio PLoS One Research Article Hearing relies on faithful signal transmission by cochlear inner hair cells (IHCs) onto auditory fibres over a wide frequency and intensity range. Exocytosis at IHC ribbon synapses is triggered by Ca(2+) inflow through Ca(V)1.3 (L-type) Ca(2+) channels. We investigated the macroscopic (whole-cell) and elementary (cell-attached) properties of Ca(2+) currents in IHCs positioned at the middle turn (frequency ∼2 kHz) of the adult gerbil cochlea, which is their most sensitive hearing region. Using near physiological recordings conditions (body temperature and a Na(+) based extracellular solution), we found that the macroscopic Ca(2+) current activates and deactivates very rapidly (time constant below 1 ms) and inactivates slowly and only partially. Single-channel recordings showed an elementary conductance of 15 pS, a sub-ms latency to first opening, and a very low steady-state open probability (P (o): 0.024 in response to 500-ms depolarizing steps at ∼−18 mV). The value of P (o) was significantly larger (0.06) in the first 40 ms of membrane depolarization, which corresponds to the time when most Ca(2+) channel openings occurred clustered in bursts (mean burst duration: 19 ms). Both the P (o) and the mean burst duration were smaller than those previously reported in high-frequency basal IHCs. Finally, we found that middle turn IHCs are likely to express about 4 times more Ca(2+) channels per ribbon than basal cells. We propose that middle-turn IHCs finely-tune Ca(V)1.3 Ca(2+) channel gating in order to provide reliable information upon timing and intensity of lower-frequency sounds. Public Library of Science 2014-11-19 /pmc/articles/PMC4237458/ /pubmed/25409445 http://dx.doi.org/10.1371/journal.pone.0113750 Text en © 2014 Zampini et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Zampini, Valeria Johnson, Stuart L. Franz, Christoph Knipper, Marlies Holley, Matthew C. Magistretti, Jacopo Russo, Giancarlo Marcotti, Walter Masetto, Sergio Fine Tuning of Ca(V)1.3 Ca(2+) Channel Properties in Adult Inner Hair Cells Positioned in the Most Sensitive Region of the Gerbil Cochlea |
title | Fine Tuning of Ca(V)1.3 Ca(2+) Channel Properties in Adult Inner Hair Cells Positioned in the Most Sensitive Region of the Gerbil Cochlea |
title_full | Fine Tuning of Ca(V)1.3 Ca(2+) Channel Properties in Adult Inner Hair Cells Positioned in the Most Sensitive Region of the Gerbil Cochlea |
title_fullStr | Fine Tuning of Ca(V)1.3 Ca(2+) Channel Properties in Adult Inner Hair Cells Positioned in the Most Sensitive Region of the Gerbil Cochlea |
title_full_unstemmed | Fine Tuning of Ca(V)1.3 Ca(2+) Channel Properties in Adult Inner Hair Cells Positioned in the Most Sensitive Region of the Gerbil Cochlea |
title_short | Fine Tuning of Ca(V)1.3 Ca(2+) Channel Properties in Adult Inner Hair Cells Positioned in the Most Sensitive Region of the Gerbil Cochlea |
title_sort | fine tuning of ca(v)1.3 ca(2+) channel properties in adult inner hair cells positioned in the most sensitive region of the gerbil cochlea |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237458/ https://www.ncbi.nlm.nih.gov/pubmed/25409445 http://dx.doi.org/10.1371/journal.pone.0113750 |
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