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Kremen1 regulates mechanosensory hair cell development in the mammalian cochlea and the zebrafish lateral line
Here we present spatio-temporal localization of Kremen1, a transmembrane receptor, in the mammalian cochlea, and investigate its role in the formation of sensory organs in mammal and fish model organisms. We show that Kremen1 is expressed in prosensory cells during cochlear development and in suppor...
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/PMC4994024/ https://www.ncbi.nlm.nih.gov/pubmed/27550540 http://dx.doi.org/10.1038/srep31668 |
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author | Mulvaney, Joanna F. Thompkins, Cathrine Noda, Teppei Nishimura, Koji Sun, Willy W. Lin, Shuh-Yow Coffin, Allison Dabdoub, Alain |
author_facet | Mulvaney, Joanna F. Thompkins, Cathrine Noda, Teppei Nishimura, Koji Sun, Willy W. Lin, Shuh-Yow Coffin, Allison Dabdoub, Alain |
author_sort | Mulvaney, Joanna F. |
collection | PubMed |
description | Here we present spatio-temporal localization of Kremen1, a transmembrane receptor, in the mammalian cochlea, and investigate its role in the formation of sensory organs in mammal and fish model organisms. We show that Kremen1 is expressed in prosensory cells during cochlear development and in supporting cells of the adult mouse cochlea. Based on this expression pattern, we investigated whether Kremen1 functions to modulate cell fate decisions in the prosensory domain of the developing cochlea. We used gain and loss-of-function experiments to show that Kremen1 is sufficient to bias cells towards supporting cell fate, and is implicated in suppression of hair cell formation. In addition to our findings in the mouse cochlea, we examined the effects of over expression and loss of Kremen1 in the zebrafish lateral line. In agreement with our mouse data, we show that over expression of Kremen1 has a negative effect on the number of mechanosensory cells that form in the zebrafish neuromasts, and that fish lacking Kremen1 protein develop more hair cells per neuromast compared to wild type fish. Collectively, these data support an inhibitory role for Kremen1 in hair cell fate specification. |
format | Online Article Text |
id | pubmed-4994024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49940242016-08-30 Kremen1 regulates mechanosensory hair cell development in the mammalian cochlea and the zebrafish lateral line Mulvaney, Joanna F. Thompkins, Cathrine Noda, Teppei Nishimura, Koji Sun, Willy W. Lin, Shuh-Yow Coffin, Allison Dabdoub, Alain Sci Rep Article Here we present spatio-temporal localization of Kremen1, a transmembrane receptor, in the mammalian cochlea, and investigate its role in the formation of sensory organs in mammal and fish model organisms. We show that Kremen1 is expressed in prosensory cells during cochlear development and in supporting cells of the adult mouse cochlea. Based on this expression pattern, we investigated whether Kremen1 functions to modulate cell fate decisions in the prosensory domain of the developing cochlea. We used gain and loss-of-function experiments to show that Kremen1 is sufficient to bias cells towards supporting cell fate, and is implicated in suppression of hair cell formation. In addition to our findings in the mouse cochlea, we examined the effects of over expression and loss of Kremen1 in the zebrafish lateral line. In agreement with our mouse data, we show that over expression of Kremen1 has a negative effect on the number of mechanosensory cells that form in the zebrafish neuromasts, and that fish lacking Kremen1 protein develop more hair cells per neuromast compared to wild type fish. Collectively, these data support an inhibitory role for Kremen1 in hair cell fate specification. Nature Publishing Group 2016-08-23 /pmc/articles/PMC4994024/ /pubmed/27550540 http://dx.doi.org/10.1038/srep31668 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 Mulvaney, Joanna F. Thompkins, Cathrine Noda, Teppei Nishimura, Koji Sun, Willy W. Lin, Shuh-Yow Coffin, Allison Dabdoub, Alain Kremen1 regulates mechanosensory hair cell development in the mammalian cochlea and the zebrafish lateral line |
title | Kremen1 regulates mechanosensory hair cell development in the mammalian cochlea and the zebrafish lateral line |
title_full | Kremen1 regulates mechanosensory hair cell development in the mammalian cochlea and the zebrafish lateral line |
title_fullStr | Kremen1 regulates mechanosensory hair cell development in the mammalian cochlea and the zebrafish lateral line |
title_full_unstemmed | Kremen1 regulates mechanosensory hair cell development in the mammalian cochlea and the zebrafish lateral line |
title_short | Kremen1 regulates mechanosensory hair cell development in the mammalian cochlea and the zebrafish lateral line |
title_sort | kremen1 regulates mechanosensory hair cell development in the mammalian cochlea and the zebrafish lateral line |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4994024/ https://www.ncbi.nlm.nih.gov/pubmed/27550540 http://dx.doi.org/10.1038/srep31668 |
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