Cargando…

Canonical Notch signaling plays an instructive role in auditory supporting cell development

The auditory sensory epithelium, composed of mechano-sensory hair cells (HCs) and highly specialized glial-like supporting cells (SCs), is critical for our ability to detect sound. SCs provide structural and functional support to HCs and play an essential role in cochlear development, homeostasis an...

Descripción completa

Detalles Bibliográficos
Autores principales: Campbell, Dean P., Chrysostomou, Elena, Doetzlhofer, Angelika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726253/
https://www.ncbi.nlm.nih.gov/pubmed/26786414
http://dx.doi.org/10.1038/srep19484
_version_ 1782411781749080064
author Campbell, Dean P.
Chrysostomou, Elena
Doetzlhofer, Angelika
author_facet Campbell, Dean P.
Chrysostomou, Elena
Doetzlhofer, Angelika
author_sort Campbell, Dean P.
collection PubMed
description The auditory sensory epithelium, composed of mechano-sensory hair cells (HCs) and highly specialized glial-like supporting cells (SCs), is critical for our ability to detect sound. SCs provide structural and functional support to HCs and play an essential role in cochlear development, homeostasis and repair. Despite their importance, however, surprisingly little is known about the molecular mechanisms guiding SC differentiation. Here, we provide evidence that in addition to its well-characterized inhibitory function, canonical Notch signaling plays a positive, instructive role in the differentiation of SCs. Using γ-secretase inhibitor DAPT to acutely block canonical Notch signaling, we identified a cohort of Notch-regulated SC-specific genes, with diverse functions in cell signaling, cell differentiation, neuronal innervation and synaptogenesis. We validated the newly identified Notch-regulated genes in vivo using genetic gain (Emx2(Cre/+); Rosa26(N1ICD/+)) and loss-of-function approaches (Emx2(Cre/+); Rosa26(DnMAML1/+)). Furthermore, we demonstrate that Notch over-activation in the differentiating murine cochlea (Emx2(Cre/+); Rosa26(N1ICD/+)) actively promotes a SC-specific gene expression program. Finally, we show that outer SCs –so called Deiters’ cells are selectively lost by prolonged reduction (Emx2(Cre/+); Rosa26(DnMAML1/+/+)) or abolishment of canonical Notch signaling (Fgfr3-iCreER; Rbpj(−/Δ)), indicating a critical role for Notch signaling in Deiters’ cell development.
format Online
Article
Text
id pubmed-4726253
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-47262532016-01-27 Canonical Notch signaling plays an instructive role in auditory supporting cell development Campbell, Dean P. Chrysostomou, Elena Doetzlhofer, Angelika Sci Rep Article The auditory sensory epithelium, composed of mechano-sensory hair cells (HCs) and highly specialized glial-like supporting cells (SCs), is critical for our ability to detect sound. SCs provide structural and functional support to HCs and play an essential role in cochlear development, homeostasis and repair. Despite their importance, however, surprisingly little is known about the molecular mechanisms guiding SC differentiation. Here, we provide evidence that in addition to its well-characterized inhibitory function, canonical Notch signaling plays a positive, instructive role in the differentiation of SCs. Using γ-secretase inhibitor DAPT to acutely block canonical Notch signaling, we identified a cohort of Notch-regulated SC-specific genes, with diverse functions in cell signaling, cell differentiation, neuronal innervation and synaptogenesis. We validated the newly identified Notch-regulated genes in vivo using genetic gain (Emx2(Cre/+); Rosa26(N1ICD/+)) and loss-of-function approaches (Emx2(Cre/+); Rosa26(DnMAML1/+)). Furthermore, we demonstrate that Notch over-activation in the differentiating murine cochlea (Emx2(Cre/+); Rosa26(N1ICD/+)) actively promotes a SC-specific gene expression program. Finally, we show that outer SCs –so called Deiters’ cells are selectively lost by prolonged reduction (Emx2(Cre/+); Rosa26(DnMAML1/+/+)) or abolishment of canonical Notch signaling (Fgfr3-iCreER; Rbpj(−/Δ)), indicating a critical role for Notch signaling in Deiters’ cell development. Nature Publishing Group 2016-01-20 /pmc/articles/PMC4726253/ /pubmed/26786414 http://dx.doi.org/10.1038/srep19484 Text en Copyright © 2016, Macmillan Publishers Limited 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
Campbell, Dean P.
Chrysostomou, Elena
Doetzlhofer, Angelika
Canonical Notch signaling plays an instructive role in auditory supporting cell development
title Canonical Notch signaling plays an instructive role in auditory supporting cell development
title_full Canonical Notch signaling plays an instructive role in auditory supporting cell development
title_fullStr Canonical Notch signaling plays an instructive role in auditory supporting cell development
title_full_unstemmed Canonical Notch signaling plays an instructive role in auditory supporting cell development
title_short Canonical Notch signaling plays an instructive role in auditory supporting cell development
title_sort canonical notch signaling plays an instructive role in auditory supporting cell development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726253/
https://www.ncbi.nlm.nih.gov/pubmed/26786414
http://dx.doi.org/10.1038/srep19484
work_keys_str_mv AT campbelldeanp canonicalnotchsignalingplaysaninstructiveroleinauditorysupportingcelldevelopment
AT chrysostomouelena canonicalnotchsignalingplaysaninstructiveroleinauditorysupportingcelldevelopment
AT doetzlhoferangelika canonicalnotchsignalingplaysaninstructiveroleinauditorysupportingcelldevelopment