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Function of bidirectional sensitivity in the otolith organs established by transcription factor Emx2

Otolith organs of the inner ear are innervated by two parallel afferent projections to the brainstem and cerebellum. These innervations were proposed to segregate across the line of polarity reversal (LPR) within each otolith organ, which divides the organ into two regions of hair cells (HC) with op...

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Autores principales: Ji, Young Rae, Tona, Yosuke, Wafa, Talah, Christman, Matthew E., Tourney, Edward D., Jiang, Tao, Ohta, Sho, Cheng, Hui, Fitzgerald, Tracy, Fritzsch, Bernd, Jones, Sherri M., Cullen, Kathleen E., Wu, Doris K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9592604/
https://www.ncbi.nlm.nih.gov/pubmed/36280667
http://dx.doi.org/10.1038/s41467-022-33819-3
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author Ji, Young Rae
Tona, Yosuke
Wafa, Talah
Christman, Matthew E.
Tourney, Edward D.
Jiang, Tao
Ohta, Sho
Cheng, Hui
Fitzgerald, Tracy
Fritzsch, Bernd
Jones, Sherri M.
Cullen, Kathleen E.
Wu, Doris K.
author_facet Ji, Young Rae
Tona, Yosuke
Wafa, Talah
Christman, Matthew E.
Tourney, Edward D.
Jiang, Tao
Ohta, Sho
Cheng, Hui
Fitzgerald, Tracy
Fritzsch, Bernd
Jones, Sherri M.
Cullen, Kathleen E.
Wu, Doris K.
author_sort Ji, Young Rae
collection PubMed
description Otolith organs of the inner ear are innervated by two parallel afferent projections to the brainstem and cerebellum. These innervations were proposed to segregate across the line of polarity reversal (LPR) within each otolith organ, which divides the organ into two regions of hair cells (HC) with opposite stereociliary orientation. The relationship and functional significance of these anatomical features are not known. Here, we show regional expression of Emx2 in otolith organs, which establishes LPR, mediates the neuronal segregation across LPR and constitutes the bidirectional sensitivity function. Conditional knockout (cKO) of Emx2 in HCs lacks LPR. Tmie cKO, in which mechanotransduction was abolished selectively in HCs within the Emx2 expression domain also lacks bidirectional sensitivity. Analyses of both mutants indicate that LPR is specifically required for mice to swim comfortably and to traverse a balance beam efficiently, but LPR is not required for mice to stay on a rotating rod.
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spelling pubmed-95926042022-10-26 Function of bidirectional sensitivity in the otolith organs established by transcription factor Emx2 Ji, Young Rae Tona, Yosuke Wafa, Talah Christman, Matthew E. Tourney, Edward D. Jiang, Tao Ohta, Sho Cheng, Hui Fitzgerald, Tracy Fritzsch, Bernd Jones, Sherri M. Cullen, Kathleen E. Wu, Doris K. Nat Commun Article Otolith organs of the inner ear are innervated by two parallel afferent projections to the brainstem and cerebellum. These innervations were proposed to segregate across the line of polarity reversal (LPR) within each otolith organ, which divides the organ into two regions of hair cells (HC) with opposite stereociliary orientation. The relationship and functional significance of these anatomical features are not known. Here, we show regional expression of Emx2 in otolith organs, which establishes LPR, mediates the neuronal segregation across LPR and constitutes the bidirectional sensitivity function. Conditional knockout (cKO) of Emx2 in HCs lacks LPR. Tmie cKO, in which mechanotransduction was abolished selectively in HCs within the Emx2 expression domain also lacks bidirectional sensitivity. Analyses of both mutants indicate that LPR is specifically required for mice to swim comfortably and to traverse a balance beam efficiently, but LPR is not required for mice to stay on a rotating rod. Nature Publishing Group UK 2022-10-24 /pmc/articles/PMC9592604/ /pubmed/36280667 http://dx.doi.org/10.1038/s41467-022-33819-3 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ji, Young Rae
Tona, Yosuke
Wafa, Talah
Christman, Matthew E.
Tourney, Edward D.
Jiang, Tao
Ohta, Sho
Cheng, Hui
Fitzgerald, Tracy
Fritzsch, Bernd
Jones, Sherri M.
Cullen, Kathleen E.
Wu, Doris K.
Function of bidirectional sensitivity in the otolith organs established by transcription factor Emx2
title Function of bidirectional sensitivity in the otolith organs established by transcription factor Emx2
title_full Function of bidirectional sensitivity in the otolith organs established by transcription factor Emx2
title_fullStr Function of bidirectional sensitivity in the otolith organs established by transcription factor Emx2
title_full_unstemmed Function of bidirectional sensitivity in the otolith organs established by transcription factor Emx2
title_short Function of bidirectional sensitivity in the otolith organs established by transcription factor Emx2
title_sort function of bidirectional sensitivity in the otolith organs established by transcription factor emx2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9592604/
https://www.ncbi.nlm.nih.gov/pubmed/36280667
http://dx.doi.org/10.1038/s41467-022-33819-3
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