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Molecular bases of K(+) secretory cells in the inner ear: shared and distinct features between birds and mammals

In the cochlea, mammals maintain a uniquely high endolymphatic potential (EP), which is not observed in other vertebrate groups. However, a high [K(+)] is always present in the inner ear endolymph. Here, we show that Kir4.1, which is required in the mammalian stria vascularis to generate the highly...

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Autores principales: Wilms, Viviane, Köppl, Christine, Söffgen, Chris, Hartmann, Anna-Maria, Nothwang, Hans Gerd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5041087/
https://www.ncbi.nlm.nih.gov/pubmed/27680950
http://dx.doi.org/10.1038/srep34203
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author Wilms, Viviane
Köppl, Christine
Söffgen, Chris
Hartmann, Anna-Maria
Nothwang, Hans Gerd
author_facet Wilms, Viviane
Köppl, Christine
Söffgen, Chris
Hartmann, Anna-Maria
Nothwang, Hans Gerd
author_sort Wilms, Viviane
collection PubMed
description In the cochlea, mammals maintain a uniquely high endolymphatic potential (EP), which is not observed in other vertebrate groups. However, a high [K(+)] is always present in the inner ear endolymph. Here, we show that Kir4.1, which is required in the mammalian stria vascularis to generate the highly positive EP, is absent in the functionally equivalent avian tegmentum vasculosum. In contrast, the molecular repertoire required for K(+) secretion, specifically NKCC1, KCNQ1, KCNE1, BSND and CLC-K, is shared between the tegmentum vasculosum, the vestibular dark cells and the marginal cells of the stria vascularis. We further show that in barn owls, the tegmentum vasculosum is enlarged and a higher EP (~+34 mV) maintained, compared to other birds. Our data suggest that both the tegmentum vasculosum and the stratified stria vascularis evolved from an ancestral vestibular epithelium that already featured the major cell types of the auditory epithelia. Genetic recruitment of Kir4.1 specifically to strial melanocytes was then a crucial step in mammalian evolution enabling an increase in the cochlear EP. An increased EP may be related to high-frequency hearing, as this is a hallmark of barn owls among birds and mammals among amniotes.
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spelling pubmed-50410872016-09-30 Molecular bases of K(+) secretory cells in the inner ear: shared and distinct features between birds and mammals Wilms, Viviane Köppl, Christine Söffgen, Chris Hartmann, Anna-Maria Nothwang, Hans Gerd Sci Rep Article In the cochlea, mammals maintain a uniquely high endolymphatic potential (EP), which is not observed in other vertebrate groups. However, a high [K(+)] is always present in the inner ear endolymph. Here, we show that Kir4.1, which is required in the mammalian stria vascularis to generate the highly positive EP, is absent in the functionally equivalent avian tegmentum vasculosum. In contrast, the molecular repertoire required for K(+) secretion, specifically NKCC1, KCNQ1, KCNE1, BSND and CLC-K, is shared between the tegmentum vasculosum, the vestibular dark cells and the marginal cells of the stria vascularis. We further show that in barn owls, the tegmentum vasculosum is enlarged and a higher EP (~+34 mV) maintained, compared to other birds. Our data suggest that both the tegmentum vasculosum and the stratified stria vascularis evolved from an ancestral vestibular epithelium that already featured the major cell types of the auditory epithelia. Genetic recruitment of Kir4.1 specifically to strial melanocytes was then a crucial step in mammalian evolution enabling an increase in the cochlear EP. An increased EP may be related to high-frequency hearing, as this is a hallmark of barn owls among birds and mammals among amniotes. Nature Publishing Group 2016-09-29 /pmc/articles/PMC5041087/ /pubmed/27680950 http://dx.doi.org/10.1038/srep34203 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Wilms, Viviane
Köppl, Christine
Söffgen, Chris
Hartmann, Anna-Maria
Nothwang, Hans Gerd
Molecular bases of K(+) secretory cells in the inner ear: shared and distinct features between birds and mammals
title Molecular bases of K(+) secretory cells in the inner ear: shared and distinct features between birds and mammals
title_full Molecular bases of K(+) secretory cells in the inner ear: shared and distinct features between birds and mammals
title_fullStr Molecular bases of K(+) secretory cells in the inner ear: shared and distinct features between birds and mammals
title_full_unstemmed Molecular bases of K(+) secretory cells in the inner ear: shared and distinct features between birds and mammals
title_short Molecular bases of K(+) secretory cells in the inner ear: shared and distinct features between birds and mammals
title_sort molecular bases of k(+) secretory cells in the inner ear: shared and distinct features between birds and mammals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5041087/
https://www.ncbi.nlm.nih.gov/pubmed/27680950
http://dx.doi.org/10.1038/srep34203
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