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Fine-tuning of Notch signaling sets the boundary of the organ of Corti and establishes sensory cell fates
The signals that induce the organ of Corti and define its boundaries in the cochlea are poorly understood. We show that two Notch modifiers, Lfng and Mfng, are transiently expressed precisely at the neural boundary of the organ of Corti. Cre-Lox fate mapping shows this region gives rise to inner hai...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5215100/ https://www.ncbi.nlm.nih.gov/pubmed/27966429 http://dx.doi.org/10.7554/eLife.19921 |
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author | Basch, Martin L Brown, Rogers M Jen, Hsin-I Semerci, Fatih Depreux, Frederic Edlund, Renée K Zhang, Hongyuan Norton, Christine R Gridley, Thomas Cole, Susan E Doetzlhofer, Angelika Maletic-Savatic, Mirjana Segil, Neil Groves, Andrew K |
author_facet | Basch, Martin L Brown, Rogers M Jen, Hsin-I Semerci, Fatih Depreux, Frederic Edlund, Renée K Zhang, Hongyuan Norton, Christine R Gridley, Thomas Cole, Susan E Doetzlhofer, Angelika Maletic-Savatic, Mirjana Segil, Neil Groves, Andrew K |
author_sort | Basch, Martin L |
collection | PubMed |
description | The signals that induce the organ of Corti and define its boundaries in the cochlea are poorly understood. We show that two Notch modifiers, Lfng and Mfng, are transiently expressed precisely at the neural boundary of the organ of Corti. Cre-Lox fate mapping shows this region gives rise to inner hair cells and their associated inner phalangeal cells. Mutation of Lfng and Mfng disrupts this boundary, producing unexpected duplications of inner hair cells and inner phalangeal cells. This phenotype is mimicked by other mouse mutants or pharmacological treatments that lower but not abolish Notch signaling. However, strong disruption of Notch signaling causes a very different result, generating many ectopic hair cells at the expense of inner phalangeal cells. Our results show that Notch signaling is finely calibrated in the cochlea to produce precisely tuned levels of signaling that first set the boundary of the organ of Corti and later regulate hair cell development. DOI: http://dx.doi.org/10.7554/eLife.19921.001 |
format | Online Article Text |
id | pubmed-5215100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-52151002017-01-09 Fine-tuning of Notch signaling sets the boundary of the organ of Corti and establishes sensory cell fates Basch, Martin L Brown, Rogers M Jen, Hsin-I Semerci, Fatih Depreux, Frederic Edlund, Renée K Zhang, Hongyuan Norton, Christine R Gridley, Thomas Cole, Susan E Doetzlhofer, Angelika Maletic-Savatic, Mirjana Segil, Neil Groves, Andrew K eLife Cell Biology The signals that induce the organ of Corti and define its boundaries in the cochlea are poorly understood. We show that two Notch modifiers, Lfng and Mfng, are transiently expressed precisely at the neural boundary of the organ of Corti. Cre-Lox fate mapping shows this region gives rise to inner hair cells and their associated inner phalangeal cells. Mutation of Lfng and Mfng disrupts this boundary, producing unexpected duplications of inner hair cells and inner phalangeal cells. This phenotype is mimicked by other mouse mutants or pharmacological treatments that lower but not abolish Notch signaling. However, strong disruption of Notch signaling causes a very different result, generating many ectopic hair cells at the expense of inner phalangeal cells. Our results show that Notch signaling is finely calibrated in the cochlea to produce precisely tuned levels of signaling that first set the boundary of the organ of Corti and later regulate hair cell development. DOI: http://dx.doi.org/10.7554/eLife.19921.001 eLife Sciences Publications, Ltd 2016-12-14 /pmc/articles/PMC5215100/ /pubmed/27966429 http://dx.doi.org/10.7554/eLife.19921 Text en © 2016, Basch et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Basch, Martin L Brown, Rogers M Jen, Hsin-I Semerci, Fatih Depreux, Frederic Edlund, Renée K Zhang, Hongyuan Norton, Christine R Gridley, Thomas Cole, Susan E Doetzlhofer, Angelika Maletic-Savatic, Mirjana Segil, Neil Groves, Andrew K Fine-tuning of Notch signaling sets the boundary of the organ of Corti and establishes sensory cell fates |
title | Fine-tuning of Notch signaling sets the boundary of the organ of Corti and establishes sensory cell fates |
title_full | Fine-tuning of Notch signaling sets the boundary of the organ of Corti and establishes sensory cell fates |
title_fullStr | Fine-tuning of Notch signaling sets the boundary of the organ of Corti and establishes sensory cell fates |
title_full_unstemmed | Fine-tuning of Notch signaling sets the boundary of the organ of Corti and establishes sensory cell fates |
title_short | Fine-tuning of Notch signaling sets the boundary of the organ of Corti and establishes sensory cell fates |
title_sort | fine-tuning of notch signaling sets the boundary of the organ of corti and establishes sensory cell fates |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5215100/ https://www.ncbi.nlm.nih.gov/pubmed/27966429 http://dx.doi.org/10.7554/eLife.19921 |
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