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scRNA-Seq reveals distinct stem cell populations that drive hair cell regeneration after loss of Fgf and Notch signaling
Loss of sensory hair cells leads to deafness and balance deficiencies. In contrast to mammalian hair cells, zebrafish ear and lateral line hair cells regenerate from poorly characterized support cells. Equally ill-defined is the gene regulatory network underlying the progression of support cells to...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6363392/ https://www.ncbi.nlm.nih.gov/pubmed/30681411 http://dx.doi.org/10.7554/eLife.44431 |
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author | Lush, Mark E Diaz, Daniel C Koenecke, Nina Baek, Sungmin Boldt, Helena St Peter, Madeleine K Gaitan-Escudero, Tatiana Romero-Carvajal, Andres Busch-Nentwich, Elisabeth M Perera, Anoja G Hall, Kathryn E Peak, Allison Haug, Jeffrey S Piotrowski, Tatjana |
author_facet | Lush, Mark E Diaz, Daniel C Koenecke, Nina Baek, Sungmin Boldt, Helena St Peter, Madeleine K Gaitan-Escudero, Tatiana Romero-Carvajal, Andres Busch-Nentwich, Elisabeth M Perera, Anoja G Hall, Kathryn E Peak, Allison Haug, Jeffrey S Piotrowski, Tatjana |
author_sort | Lush, Mark E |
collection | PubMed |
description | Loss of sensory hair cells leads to deafness and balance deficiencies. In contrast to mammalian hair cells, zebrafish ear and lateral line hair cells regenerate from poorly characterized support cells. Equally ill-defined is the gene regulatory network underlying the progression of support cells to differentiated hair cells. scRNA-Seq of lateral line organs uncovered five different support cell types, including quiescent and activated stem cells. Ordering of support cells along a developmental trajectory identified self-renewing cells and genes required for hair cell differentiation. scRNA-Seq analyses of fgf3 mutants, in which hair cell regeneration is increased, demonstrates that Fgf and Notch signaling inhibit proliferation of support cells in parallel by inhibiting Wnt signaling. Our scRNA-Seq analyses set the foundation for mechanistic studies of sensory organ regeneration and is crucial for identifying factors to trigger hair cell production in mammals. The data is searchable and publicly accessible via a web-based interface. |
format | Online Article Text |
id | pubmed-6363392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-63633922019-02-06 scRNA-Seq reveals distinct stem cell populations that drive hair cell regeneration after loss of Fgf and Notch signaling Lush, Mark E Diaz, Daniel C Koenecke, Nina Baek, Sungmin Boldt, Helena St Peter, Madeleine K Gaitan-Escudero, Tatiana Romero-Carvajal, Andres Busch-Nentwich, Elisabeth M Perera, Anoja G Hall, Kathryn E Peak, Allison Haug, Jeffrey S Piotrowski, Tatjana eLife Developmental Biology Loss of sensory hair cells leads to deafness and balance deficiencies. In contrast to mammalian hair cells, zebrafish ear and lateral line hair cells regenerate from poorly characterized support cells. Equally ill-defined is the gene regulatory network underlying the progression of support cells to differentiated hair cells. scRNA-Seq of lateral line organs uncovered five different support cell types, including quiescent and activated stem cells. Ordering of support cells along a developmental trajectory identified self-renewing cells and genes required for hair cell differentiation. scRNA-Seq analyses of fgf3 mutants, in which hair cell regeneration is increased, demonstrates that Fgf and Notch signaling inhibit proliferation of support cells in parallel by inhibiting Wnt signaling. Our scRNA-Seq analyses set the foundation for mechanistic studies of sensory organ regeneration and is crucial for identifying factors to trigger hair cell production in mammals. The data is searchable and publicly accessible via a web-based interface. eLife Sciences Publications, Ltd 2019-01-25 /pmc/articles/PMC6363392/ /pubmed/30681411 http://dx.doi.org/10.7554/eLife.44431 Text en © 2019, Lush et al http://creativecommons.org/licenses/by/4.0/ 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 | Developmental Biology Lush, Mark E Diaz, Daniel C Koenecke, Nina Baek, Sungmin Boldt, Helena St Peter, Madeleine K Gaitan-Escudero, Tatiana Romero-Carvajal, Andres Busch-Nentwich, Elisabeth M Perera, Anoja G Hall, Kathryn E Peak, Allison Haug, Jeffrey S Piotrowski, Tatjana scRNA-Seq reveals distinct stem cell populations that drive hair cell regeneration after loss of Fgf and Notch signaling |
title | scRNA-Seq reveals distinct stem cell populations that drive hair cell regeneration after loss of Fgf and Notch signaling |
title_full | scRNA-Seq reveals distinct stem cell populations that drive hair cell regeneration after loss of Fgf and Notch signaling |
title_fullStr | scRNA-Seq reveals distinct stem cell populations that drive hair cell regeneration after loss of Fgf and Notch signaling |
title_full_unstemmed | scRNA-Seq reveals distinct stem cell populations that drive hair cell regeneration after loss of Fgf and Notch signaling |
title_short | scRNA-Seq reveals distinct stem cell populations that drive hair cell regeneration after loss of Fgf and Notch signaling |
title_sort | scrna-seq reveals distinct stem cell populations that drive hair cell regeneration after loss of fgf and notch signaling |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6363392/ https://www.ncbi.nlm.nih.gov/pubmed/30681411 http://dx.doi.org/10.7554/eLife.44431 |
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