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Functional development of mechanosensitive hair cells in stem cell-derived organoids parallels native vestibular hair cells
Inner ear sensory epithelia contain mechanosensitive hair cells that transmit information to the brain through innervation with bipolar neurons. Mammalian hair cells do not regenerate and are limited in number. Here we investigate the potential to generate mechanosensitive hair cells from mouse embr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4890183/ https://www.ncbi.nlm.nih.gov/pubmed/27215798 http://dx.doi.org/10.1038/ncomms11508 |
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author | Liu, Xiao-Ping Koehler, Karl R. Mikosz, Andrew M. Hashino, Eri Holt, Jeffrey R. |
author_facet | Liu, Xiao-Ping Koehler, Karl R. Mikosz, Andrew M. Hashino, Eri Holt, Jeffrey R. |
author_sort | Liu, Xiao-Ping |
collection | PubMed |
description | Inner ear sensory epithelia contain mechanosensitive hair cells that transmit information to the brain through innervation with bipolar neurons. Mammalian hair cells do not regenerate and are limited in number. Here we investigate the potential to generate mechanosensitive hair cells from mouse embryonic stem cells in a three-dimensional (3D) culture system. The system faithfully recapitulates mouse inner ear induction followed by self-guided development into organoids that morphologically resemble inner ear vestibular organs. We find that organoid hair cells acquire mechanosensitivity equivalent to functionally mature hair cells in postnatal mice. The organoid hair cells also progress through a similar dynamic developmental pattern of ion channel expression, reminiscent of two subtypes of native vestibular hair cells. We conclude that our 3D culture system can generate large numbers of fully functional sensory cells which could be used to investigate mechanisms of inner ear development and disease as well as regenerative mechanisms for inner ear repair. |
format | Online Article Text |
id | pubmed-4890183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48901832016-06-10 Functional development of mechanosensitive hair cells in stem cell-derived organoids parallels native vestibular hair cells Liu, Xiao-Ping Koehler, Karl R. Mikosz, Andrew M. Hashino, Eri Holt, Jeffrey R. Nat Commun Article Inner ear sensory epithelia contain mechanosensitive hair cells that transmit information to the brain through innervation with bipolar neurons. Mammalian hair cells do not regenerate and are limited in number. Here we investigate the potential to generate mechanosensitive hair cells from mouse embryonic stem cells in a three-dimensional (3D) culture system. The system faithfully recapitulates mouse inner ear induction followed by self-guided development into organoids that morphologically resemble inner ear vestibular organs. We find that organoid hair cells acquire mechanosensitivity equivalent to functionally mature hair cells in postnatal mice. The organoid hair cells also progress through a similar dynamic developmental pattern of ion channel expression, reminiscent of two subtypes of native vestibular hair cells. We conclude that our 3D culture system can generate large numbers of fully functional sensory cells which could be used to investigate mechanisms of inner ear development and disease as well as regenerative mechanisms for inner ear repair. Nature Publishing Group 2016-05-24 /pmc/articles/PMC4890183/ /pubmed/27215798 http://dx.doi.org/10.1038/ncomms11508 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 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 Liu, Xiao-Ping Koehler, Karl R. Mikosz, Andrew M. Hashino, Eri Holt, Jeffrey R. Functional development of mechanosensitive hair cells in stem cell-derived organoids parallels native vestibular hair cells |
title | Functional development of mechanosensitive hair cells in stem cell-derived organoids parallels native vestibular hair cells |
title_full | Functional development of mechanosensitive hair cells in stem cell-derived organoids parallels native vestibular hair cells |
title_fullStr | Functional development of mechanosensitive hair cells in stem cell-derived organoids parallels native vestibular hair cells |
title_full_unstemmed | Functional development of mechanosensitive hair cells in stem cell-derived organoids parallels native vestibular hair cells |
title_short | Functional development of mechanosensitive hair cells in stem cell-derived organoids parallels native vestibular hair cells |
title_sort | functional development of mechanosensitive hair cells in stem cell-derived organoids parallels native vestibular hair cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4890183/ https://www.ncbi.nlm.nih.gov/pubmed/27215798 http://dx.doi.org/10.1038/ncomms11508 |
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