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Requirement for Jagged1-Notch2 signaling in patterning the bones of the mouse and human middle ear
Whereas Jagged1-Notch2 signaling is known to pattern the sensorineural components of the inner ear, its role in middle ear development has been less clear. We previously reported a role for Jagged-Notch signaling in shaping skeletal elements derived from the first two pharyngeal arches of zebrafish....
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5451394/ https://www.ncbi.nlm.nih.gov/pubmed/28566723 http://dx.doi.org/10.1038/s41598-017-02574-7 |
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author | Teng, Camilla S. Yen, Hai-Yun Barske, Lindsey Smith, Bea Llamas, Juan Segil, Neil Go, John Sanchez-Lara, Pedro A. Maxson, Robert E. Crump, J. Gage |
author_facet | Teng, Camilla S. Yen, Hai-Yun Barske, Lindsey Smith, Bea Llamas, Juan Segil, Neil Go, John Sanchez-Lara, Pedro A. Maxson, Robert E. Crump, J. Gage |
author_sort | Teng, Camilla S. |
collection | PubMed |
description | Whereas Jagged1-Notch2 signaling is known to pattern the sensorineural components of the inner ear, its role in middle ear development has been less clear. We previously reported a role for Jagged-Notch signaling in shaping skeletal elements derived from the first two pharyngeal arches of zebrafish. Here we show a conserved requirement for Jagged1-Notch2 signaling in patterning the stapes and incus middle ear bones derived from the equivalent pharyngeal arches of mammals. Mice lacking Jagged1 or Notch2 in neural crest-derived cells (NCCs) of the pharyngeal arches display a malformed stapes. Heterozygous Jagged1 knockout mice, a model for Alagille Syndrome (AGS), also display stapes and incus defects. We find that Jagged1-Notch2 signaling functions early to pattern the stapes cartilage template, with stapes malformations correlating with hearing loss across all frequencies. We observe similar stapes defects and hearing loss in one patient with heterozygous JAGGED1 loss, and a diversity of conductive and sensorineural hearing loss in nearly half of AGS patients, many of which carry JAGGED1 mutations. Our findings reveal deep conservation of Jagged1-Notch2 signaling in patterning the pharyngeal arches from fish to mouse to man, despite the very different functions of their skeletal derivatives in jaw support and sound transduction. |
format | Online Article Text |
id | pubmed-5451394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54513942017-06-01 Requirement for Jagged1-Notch2 signaling in patterning the bones of the mouse and human middle ear Teng, Camilla S. Yen, Hai-Yun Barske, Lindsey Smith, Bea Llamas, Juan Segil, Neil Go, John Sanchez-Lara, Pedro A. Maxson, Robert E. Crump, J. Gage Sci Rep Article Whereas Jagged1-Notch2 signaling is known to pattern the sensorineural components of the inner ear, its role in middle ear development has been less clear. We previously reported a role for Jagged-Notch signaling in shaping skeletal elements derived from the first two pharyngeal arches of zebrafish. Here we show a conserved requirement for Jagged1-Notch2 signaling in patterning the stapes and incus middle ear bones derived from the equivalent pharyngeal arches of mammals. Mice lacking Jagged1 or Notch2 in neural crest-derived cells (NCCs) of the pharyngeal arches display a malformed stapes. Heterozygous Jagged1 knockout mice, a model for Alagille Syndrome (AGS), also display stapes and incus defects. We find that Jagged1-Notch2 signaling functions early to pattern the stapes cartilage template, with stapes malformations correlating with hearing loss across all frequencies. We observe similar stapes defects and hearing loss in one patient with heterozygous JAGGED1 loss, and a diversity of conductive and sensorineural hearing loss in nearly half of AGS patients, many of which carry JAGGED1 mutations. Our findings reveal deep conservation of Jagged1-Notch2 signaling in patterning the pharyngeal arches from fish to mouse to man, despite the very different functions of their skeletal derivatives in jaw support and sound transduction. Nature Publishing Group UK 2017-05-31 /pmc/articles/PMC5451394/ /pubmed/28566723 http://dx.doi.org/10.1038/s41598-017-02574-7 Text en © The Author(s) 2017 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/. |
spellingShingle | Article Teng, Camilla S. Yen, Hai-Yun Barske, Lindsey Smith, Bea Llamas, Juan Segil, Neil Go, John Sanchez-Lara, Pedro A. Maxson, Robert E. Crump, J. Gage Requirement for Jagged1-Notch2 signaling in patterning the bones of the mouse and human middle ear |
title | Requirement for Jagged1-Notch2 signaling in patterning the bones of the mouse and human middle ear |
title_full | Requirement for Jagged1-Notch2 signaling in patterning the bones of the mouse and human middle ear |
title_fullStr | Requirement for Jagged1-Notch2 signaling in patterning the bones of the mouse and human middle ear |
title_full_unstemmed | Requirement for Jagged1-Notch2 signaling in patterning the bones of the mouse and human middle ear |
title_short | Requirement for Jagged1-Notch2 signaling in patterning the bones of the mouse and human middle ear |
title_sort | requirement for jagged1-notch2 signaling in patterning the bones of the mouse and human middle ear |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5451394/ https://www.ncbi.nlm.nih.gov/pubmed/28566723 http://dx.doi.org/10.1038/s41598-017-02574-7 |
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