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Neuroplastin expression is essential for hearing and hair cell PMCA expression

Hearing deficits impact on the communication with the external world and severely compromise perception of the surrounding. Deafness can be caused by particular mutations in the neuroplastin (Nptn) gene, which encodes a transmembrane recognition molecule of the immunoglobulin (Ig) superfamily and pl...

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Autores principales: Lin, Xiao, Brunk, Michael G. K., Yuanxiang, Pingan, Curran, Andrew W., Zhang, Enqi, Stöber, Franziska, Goldschmidt, Jürgen, Gundelfinger, Eckart D., Vollmer, Maike, Happel, Max F. K., Herrera-Molina, Rodrigo, Montag, Dirk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8096745/
https://www.ncbi.nlm.nih.gov/pubmed/33844052
http://dx.doi.org/10.1007/s00429-021-02269-w
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author Lin, Xiao
Brunk, Michael G. K.
Yuanxiang, Pingan
Curran, Andrew W.
Zhang, Enqi
Stöber, Franziska
Goldschmidt, Jürgen
Gundelfinger, Eckart D.
Vollmer, Maike
Happel, Max F. K.
Herrera-Molina, Rodrigo
Montag, Dirk
author_facet Lin, Xiao
Brunk, Michael G. K.
Yuanxiang, Pingan
Curran, Andrew W.
Zhang, Enqi
Stöber, Franziska
Goldschmidt, Jürgen
Gundelfinger, Eckart D.
Vollmer, Maike
Happel, Max F. K.
Herrera-Molina, Rodrigo
Montag, Dirk
author_sort Lin, Xiao
collection PubMed
description Hearing deficits impact on the communication with the external world and severely compromise perception of the surrounding. Deafness can be caused by particular mutations in the neuroplastin (Nptn) gene, which encodes a transmembrane recognition molecule of the immunoglobulin (Ig) superfamily and plasma membrane Calcium ATPase (PMCA) accessory subunit. This study investigates whether the complete absence of neuroplastin or the loss of neuroplastin in the adult after normal development lead to hearing impairment in mice analyzed by behavioral, electrophysiological, and in vivo imaging measurements. Auditory brainstem recordings from adult neuroplastin-deficient mice (Nptn(−/−)) show that these mice are deaf. With age, hair cells and spiral ganglion cells degenerate in Nptn(−/−) mice. Adult Nptn(−/−) mice fail to behaviorally respond to white noise and show reduced baseline blood flow in the auditory cortex (AC) as revealed by single-photon emission computed tomography (SPECT). In adult Nptn(−/−) mice, tone-evoked cortical activity was not detectable within the primary auditory field (A1) of the AC, although we observed non-persistent tone-like evoked activities in electrophysiological recordings of some young Nptn(−/−) mice. Conditional ablation of neuroplastin in Nptn(lox/loxEmx1Cre) mice reveals that behavioral responses to simple tones or white noise do not require neuroplastin expression by central glutamatergic neurons. Loss of neuroplastin from hair cells in adult Nptn(Δlox/loxPrCreERT) mice after normal development is correlated with increased hearing thresholds and only high prepulse intensities result in effective prepulse inhibition (PPI) of the startle response. Furthermore, we show that neuroplastin is required for the expression of PMCA 2 in outer hair cells. This suggests that altered Ca(2+) homeostasis underlies the observed hearing impairments and leads to hair cell degeneration. Our results underline the importance of neuroplastin for the development and the maintenance of the auditory system. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00429-021-02269-w.
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spelling pubmed-80967452021-05-05 Neuroplastin expression is essential for hearing and hair cell PMCA expression Lin, Xiao Brunk, Michael G. K. Yuanxiang, Pingan Curran, Andrew W. Zhang, Enqi Stöber, Franziska Goldschmidt, Jürgen Gundelfinger, Eckart D. Vollmer, Maike Happel, Max F. K. Herrera-Molina, Rodrigo Montag, Dirk Brain Struct Funct Original Article Hearing deficits impact on the communication with the external world and severely compromise perception of the surrounding. Deafness can be caused by particular mutations in the neuroplastin (Nptn) gene, which encodes a transmembrane recognition molecule of the immunoglobulin (Ig) superfamily and plasma membrane Calcium ATPase (PMCA) accessory subunit. This study investigates whether the complete absence of neuroplastin or the loss of neuroplastin in the adult after normal development lead to hearing impairment in mice analyzed by behavioral, electrophysiological, and in vivo imaging measurements. Auditory brainstem recordings from adult neuroplastin-deficient mice (Nptn(−/−)) show that these mice are deaf. With age, hair cells and spiral ganglion cells degenerate in Nptn(−/−) mice. Adult Nptn(−/−) mice fail to behaviorally respond to white noise and show reduced baseline blood flow in the auditory cortex (AC) as revealed by single-photon emission computed tomography (SPECT). In adult Nptn(−/−) mice, tone-evoked cortical activity was not detectable within the primary auditory field (A1) of the AC, although we observed non-persistent tone-like evoked activities in electrophysiological recordings of some young Nptn(−/−) mice. Conditional ablation of neuroplastin in Nptn(lox/loxEmx1Cre) mice reveals that behavioral responses to simple tones or white noise do not require neuroplastin expression by central glutamatergic neurons. Loss of neuroplastin from hair cells in adult Nptn(Δlox/loxPrCreERT) mice after normal development is correlated with increased hearing thresholds and only high prepulse intensities result in effective prepulse inhibition (PPI) of the startle response. Furthermore, we show that neuroplastin is required for the expression of PMCA 2 in outer hair cells. This suggests that altered Ca(2+) homeostasis underlies the observed hearing impairments and leads to hair cell degeneration. Our results underline the importance of neuroplastin for the development and the maintenance of the auditory system. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00429-021-02269-w. Springer Berlin Heidelberg 2021-04-12 2021 /pmc/articles/PMC8096745/ /pubmed/33844052 http://dx.doi.org/10.1007/s00429-021-02269-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Lin, Xiao
Brunk, Michael G. K.
Yuanxiang, Pingan
Curran, Andrew W.
Zhang, Enqi
Stöber, Franziska
Goldschmidt, Jürgen
Gundelfinger, Eckart D.
Vollmer, Maike
Happel, Max F. K.
Herrera-Molina, Rodrigo
Montag, Dirk
Neuroplastin expression is essential for hearing and hair cell PMCA expression
title Neuroplastin expression is essential for hearing and hair cell PMCA expression
title_full Neuroplastin expression is essential for hearing and hair cell PMCA expression
title_fullStr Neuroplastin expression is essential for hearing and hair cell PMCA expression
title_full_unstemmed Neuroplastin expression is essential for hearing and hair cell PMCA expression
title_short Neuroplastin expression is essential for hearing and hair cell PMCA expression
title_sort neuroplastin expression is essential for hearing and hair cell pmca expression
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8096745/
https://www.ncbi.nlm.nih.gov/pubmed/33844052
http://dx.doi.org/10.1007/s00429-021-02269-w
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