Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
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
_version_ 1783393094751748096
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
work_keys_str_mv AT lushmarke scrnaseqrevealsdistinctstemcellpopulationsthatdrivehaircellregenerationafterlossoffgfandnotchsignaling
AT diazdanielc scrnaseqrevealsdistinctstemcellpopulationsthatdrivehaircellregenerationafterlossoffgfandnotchsignaling
AT koeneckenina scrnaseqrevealsdistinctstemcellpopulationsthatdrivehaircellregenerationafterlossoffgfandnotchsignaling
AT baeksungmin scrnaseqrevealsdistinctstemcellpopulationsthatdrivehaircellregenerationafterlossoffgfandnotchsignaling
AT boldthelena scrnaseqrevealsdistinctstemcellpopulationsthatdrivehaircellregenerationafterlossoffgfandnotchsignaling
AT stpetermadeleinek scrnaseqrevealsdistinctstemcellpopulationsthatdrivehaircellregenerationafterlossoffgfandnotchsignaling
AT gaitanescuderotatiana scrnaseqrevealsdistinctstemcellpopulationsthatdrivehaircellregenerationafterlossoffgfandnotchsignaling
AT romerocarvajalandres scrnaseqrevealsdistinctstemcellpopulationsthatdrivehaircellregenerationafterlossoffgfandnotchsignaling
AT buschnentwichelisabethm scrnaseqrevealsdistinctstemcellpopulationsthatdrivehaircellregenerationafterlossoffgfandnotchsignaling
AT pereraanojag scrnaseqrevealsdistinctstemcellpopulationsthatdrivehaircellregenerationafterlossoffgfandnotchsignaling
AT hallkathryne scrnaseqrevealsdistinctstemcellpopulationsthatdrivehaircellregenerationafterlossoffgfandnotchsignaling
AT peakallison scrnaseqrevealsdistinctstemcellpopulationsthatdrivehaircellregenerationafterlossoffgfandnotchsignaling
AT haugjeffreys scrnaseqrevealsdistinctstemcellpopulationsthatdrivehaircellregenerationafterlossoffgfandnotchsignaling
AT piotrowskitatjana scrnaseqrevealsdistinctstemcellpopulationsthatdrivehaircellregenerationafterlossoffgfandnotchsignaling