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Characterization of the development of the mouse cochlear epithelium at the single cell level
Mammalian hearing requires the development of the organ of Corti, a sensory epithelium comprising unique cell types. The limited number of each of these cell types, combined with their close proximity, has prevented characterization of individual cell types and/or their developmental progression. To...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7221106/ https://www.ncbi.nlm.nih.gov/pubmed/32404924 http://dx.doi.org/10.1038/s41467-020-16113-y |
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author | Kolla, Likhitha Kelly, Michael C. Mann, Zoe F. Anaya-Rocha, Alejandro Ellis, Kathryn Lemons, Abigail Palermo, Adam T. So, Kathy S. Mays, Joseph C. Orvis, Joshua Burns, Joseph C. Hertzano, Ronna Driver, Elizabeth C. Kelley, Matthew W. |
author_facet | Kolla, Likhitha Kelly, Michael C. Mann, Zoe F. Anaya-Rocha, Alejandro Ellis, Kathryn Lemons, Abigail Palermo, Adam T. So, Kathy S. Mays, Joseph C. Orvis, Joshua Burns, Joseph C. Hertzano, Ronna Driver, Elizabeth C. Kelley, Matthew W. |
author_sort | Kolla, Likhitha |
collection | PubMed |
description | Mammalian hearing requires the development of the organ of Corti, a sensory epithelium comprising unique cell types. The limited number of each of these cell types, combined with their close proximity, has prevented characterization of individual cell types and/or their developmental progression. To examine cochlear development more closely, we transcriptionally profile approximately 30,000 isolated mouse cochlear cells collected at four developmental time points. Here we report on the analysis of those cells including the identification of both known and unknown cell types. Trajectory analysis for OHCs indicates four phases of gene expression while fate mapping of progenitor cells suggests that OHCs and their surrounding supporting cells arise from a distinct (lateral) progenitor pool. Tgfβr1 is identified as being expressed in lateral progenitor cells and a Tgfβr1 antagonist inhibits OHC development. These results provide insights regarding cochlear development and demonstrate the potential value and application of this data set. |
format | Online Article Text |
id | pubmed-7221106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72211062020-05-15 Characterization of the development of the mouse cochlear epithelium at the single cell level Kolla, Likhitha Kelly, Michael C. Mann, Zoe F. Anaya-Rocha, Alejandro Ellis, Kathryn Lemons, Abigail Palermo, Adam T. So, Kathy S. Mays, Joseph C. Orvis, Joshua Burns, Joseph C. Hertzano, Ronna Driver, Elizabeth C. Kelley, Matthew W. Nat Commun Article Mammalian hearing requires the development of the organ of Corti, a sensory epithelium comprising unique cell types. The limited number of each of these cell types, combined with their close proximity, has prevented characterization of individual cell types and/or their developmental progression. To examine cochlear development more closely, we transcriptionally profile approximately 30,000 isolated mouse cochlear cells collected at four developmental time points. Here we report on the analysis of those cells including the identification of both known and unknown cell types. Trajectory analysis for OHCs indicates four phases of gene expression while fate mapping of progenitor cells suggests that OHCs and their surrounding supporting cells arise from a distinct (lateral) progenitor pool. Tgfβr1 is identified as being expressed in lateral progenitor cells and a Tgfβr1 antagonist inhibits OHC development. These results provide insights regarding cochlear development and demonstrate the potential value and application of this data set. Nature Publishing Group UK 2020-05-13 /pmc/articles/PMC7221106/ /pubmed/32404924 http://dx.doi.org/10.1038/s41467-020-16113-y Text en © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2020 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 Kolla, Likhitha Kelly, Michael C. Mann, Zoe F. Anaya-Rocha, Alejandro Ellis, Kathryn Lemons, Abigail Palermo, Adam T. So, Kathy S. Mays, Joseph C. Orvis, Joshua Burns, Joseph C. Hertzano, Ronna Driver, Elizabeth C. Kelley, Matthew W. Characterization of the development of the mouse cochlear epithelium at the single cell level |
title | Characterization of the development of the mouse cochlear epithelium at the single cell level |
title_full | Characterization of the development of the mouse cochlear epithelium at the single cell level |
title_fullStr | Characterization of the development of the mouse cochlear epithelium at the single cell level |
title_full_unstemmed | Characterization of the development of the mouse cochlear epithelium at the single cell level |
title_short | Characterization of the development of the mouse cochlear epithelium at the single cell level |
title_sort | characterization of the development of the mouse cochlear epithelium at the single cell level |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7221106/ https://www.ncbi.nlm.nih.gov/pubmed/32404924 http://dx.doi.org/10.1038/s41467-020-16113-y |
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