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Mechanotransduction and hyperpolarization-activated currents contribute to spontaneous activity in mouse vestibular ganglion neurons

The hyperpolarization-activated, cyclic nucleotide–sensitive current, I(h), is present in vestibular hair cells and vestibular ganglion neurons, and is required for normal balance function. We sought to identify the molecular correlates and functional relevance of I(h) in vestibular ganglion neurons...

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Autores principales: Horwitz, Geoffrey C., Risner-Janiczek, Jessica R., Holt, Jeffrey R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3971655/
https://www.ncbi.nlm.nih.gov/pubmed/24638995
http://dx.doi.org/10.1085/jgp.201311126
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author Horwitz, Geoffrey C.
Risner-Janiczek, Jessica R.
Holt, Jeffrey R.
author_facet Horwitz, Geoffrey C.
Risner-Janiczek, Jessica R.
Holt, Jeffrey R.
author_sort Horwitz, Geoffrey C.
collection PubMed
description The hyperpolarization-activated, cyclic nucleotide–sensitive current, I(h), is present in vestibular hair cells and vestibular ganglion neurons, and is required for normal balance function. We sought to identify the molecular correlates and functional relevance of I(h) in vestibular ganglion neurons. I(h) is carried by channels consisting of homo- or heteromeric assemblies of four protein subunits from the Hcn gene family. The relative expression of Hcn1–4 mRNA was examined using a quantitative reverse transcription PCR (RT-PCR) screen. Hcn2 was the most highly expressed subunit in vestibular neuron cell bodies. Immunolocalization of HCN2 revealed robust expression in cell bodies of all vestibular ganglion neurons. To characterize I(h) in vestibular neuron cell bodies and at hair cell–afferent synapses, we developed an intact, ex vivo preparation. We found robust physiological expression of I(h) in 89% of cell bodies and 100% of calyx terminals. I(h) was significantly larger in calyx terminals than in cell bodies; however, other biophysical characteristics were similar. I(h) was absent in calyces lacking Hcn1 and Hcn2, but small I(h) was still present in cell bodies, which suggests expression of an additional subunit, perhaps Hcn4. To determine the contributions of hair cell mechanotransduction and I(h) to the firing patterns of calyx terminals, we recorded action potentials in current-clamp mode. Mechanotransduction currents were modulated by hair bundle defection and application of calcium chelators to disrupt tip links. I(h) activity was modulated using ZD7288 and cAMP. We found that both hair cell transduction and I(h) contribute to the rate and regularity of spontaneous action potentials in the vestibular afferent neurons. We propose that modulation of I(h) in vestibular ganglion neurons may provide a mechanism for modulation of spontaneous activity in the vestibular periphery.
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spelling pubmed-39716552014-10-01 Mechanotransduction and hyperpolarization-activated currents contribute to spontaneous activity in mouse vestibular ganglion neurons Horwitz, Geoffrey C. Risner-Janiczek, Jessica R. Holt, Jeffrey R. J Gen Physiol Research Articles The hyperpolarization-activated, cyclic nucleotide–sensitive current, I(h), is present in vestibular hair cells and vestibular ganglion neurons, and is required for normal balance function. We sought to identify the molecular correlates and functional relevance of I(h) in vestibular ganglion neurons. I(h) is carried by channels consisting of homo- or heteromeric assemblies of four protein subunits from the Hcn gene family. The relative expression of Hcn1–4 mRNA was examined using a quantitative reverse transcription PCR (RT-PCR) screen. Hcn2 was the most highly expressed subunit in vestibular neuron cell bodies. Immunolocalization of HCN2 revealed robust expression in cell bodies of all vestibular ganglion neurons. To characterize I(h) in vestibular neuron cell bodies and at hair cell–afferent synapses, we developed an intact, ex vivo preparation. We found robust physiological expression of I(h) in 89% of cell bodies and 100% of calyx terminals. I(h) was significantly larger in calyx terminals than in cell bodies; however, other biophysical characteristics were similar. I(h) was absent in calyces lacking Hcn1 and Hcn2, but small I(h) was still present in cell bodies, which suggests expression of an additional subunit, perhaps Hcn4. To determine the contributions of hair cell mechanotransduction and I(h) to the firing patterns of calyx terminals, we recorded action potentials in current-clamp mode. Mechanotransduction currents were modulated by hair bundle defection and application of calcium chelators to disrupt tip links. I(h) activity was modulated using ZD7288 and cAMP. We found that both hair cell transduction and I(h) contribute to the rate and regularity of spontaneous action potentials in the vestibular afferent neurons. We propose that modulation of I(h) in vestibular ganglion neurons may provide a mechanism for modulation of spontaneous activity in the vestibular periphery. The Rockefeller University Press 2014-04 /pmc/articles/PMC3971655/ /pubmed/24638995 http://dx.doi.org/10.1085/jgp.201311126 Text en © 2014 Horwitz et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Horwitz, Geoffrey C.
Risner-Janiczek, Jessica R.
Holt, Jeffrey R.
Mechanotransduction and hyperpolarization-activated currents contribute to spontaneous activity in mouse vestibular ganglion neurons
title Mechanotransduction and hyperpolarization-activated currents contribute to spontaneous activity in mouse vestibular ganglion neurons
title_full Mechanotransduction and hyperpolarization-activated currents contribute to spontaneous activity in mouse vestibular ganglion neurons
title_fullStr Mechanotransduction and hyperpolarization-activated currents contribute to spontaneous activity in mouse vestibular ganglion neurons
title_full_unstemmed Mechanotransduction and hyperpolarization-activated currents contribute to spontaneous activity in mouse vestibular ganglion neurons
title_short Mechanotransduction and hyperpolarization-activated currents contribute to spontaneous activity in mouse vestibular ganglion neurons
title_sort mechanotransduction and hyperpolarization-activated currents contribute to spontaneous activity in mouse vestibular ganglion neurons
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3971655/
https://www.ncbi.nlm.nih.gov/pubmed/24638995
http://dx.doi.org/10.1085/jgp.201311126
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