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Distribution of neurosensory progenitor pools during inner ear morphogenesis unveiled by cell lineage reconstruction
Reconstructing the lineage of cells is central to understanding how the wide diversity of cell types develops. Here, we provide the neurosensory lineage reconstruction of a complex sensory organ, the inner ear, by imaging zebrafish embryos in vivo over an extended timespan, combining cell tracing an...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5243114/ https://www.ncbi.nlm.nih.gov/pubmed/28051766 http://dx.doi.org/10.7554/eLife.22268 |
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author | Dyballa, Sylvia Savy, Thierry Germann, Philipp Mikula, Karol Remesikova, Mariana Špir, Róbert Zecca, Andrea Peyriéras, Nadine Pujades, Cristina |
author_facet | Dyballa, Sylvia Savy, Thierry Germann, Philipp Mikula, Karol Remesikova, Mariana Špir, Róbert Zecca, Andrea Peyriéras, Nadine Pujades, Cristina |
author_sort | Dyballa, Sylvia |
collection | PubMed |
description | Reconstructing the lineage of cells is central to understanding how the wide diversity of cell types develops. Here, we provide the neurosensory lineage reconstruction of a complex sensory organ, the inner ear, by imaging zebrafish embryos in vivo over an extended timespan, combining cell tracing and cell fate marker expression over time. We deliver the first dynamic map of early neuronal and sensory progenitor pools in the whole otic vesicle. It highlights the remodeling of the neuronal progenitor domain upon neuroblast delamination, and reveals that the order and place of neuroblasts’ delamination from the otic epithelium prefigure their position within the SAG. Sensory and non-sensory domains harbor different proliferative activity contributing distinctly to the overall growth of the structure. Therefore, the otic vesicle case exemplifies a generic morphogenetic process where spatial and temporal cues regulate cell fate and functional organization of the rudiment of the definitive organ. DOI: http://dx.doi.org/10.7554/eLife.22268.001 |
format | Online Article Text |
id | pubmed-5243114 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-52431142017-01-23 Distribution of neurosensory progenitor pools during inner ear morphogenesis unveiled by cell lineage reconstruction Dyballa, Sylvia Savy, Thierry Germann, Philipp Mikula, Karol Remesikova, Mariana Špir, Róbert Zecca, Andrea Peyriéras, Nadine Pujades, Cristina eLife Cell Biology Reconstructing the lineage of cells is central to understanding how the wide diversity of cell types develops. Here, we provide the neurosensory lineage reconstruction of a complex sensory organ, the inner ear, by imaging zebrafish embryos in vivo over an extended timespan, combining cell tracing and cell fate marker expression over time. We deliver the first dynamic map of early neuronal and sensory progenitor pools in the whole otic vesicle. It highlights the remodeling of the neuronal progenitor domain upon neuroblast delamination, and reveals that the order and place of neuroblasts’ delamination from the otic epithelium prefigure their position within the SAG. Sensory and non-sensory domains harbor different proliferative activity contributing distinctly to the overall growth of the structure. Therefore, the otic vesicle case exemplifies a generic morphogenetic process where spatial and temporal cues regulate cell fate and functional organization of the rudiment of the definitive organ. DOI: http://dx.doi.org/10.7554/eLife.22268.001 eLife Sciences Publications, Ltd 2017-01-04 /pmc/articles/PMC5243114/ /pubmed/28051766 http://dx.doi.org/10.7554/eLife.22268 Text en © 2017, Dyballa et al 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 | Cell Biology Dyballa, Sylvia Savy, Thierry Germann, Philipp Mikula, Karol Remesikova, Mariana Špir, Róbert Zecca, Andrea Peyriéras, Nadine Pujades, Cristina Distribution of neurosensory progenitor pools during inner ear morphogenesis unveiled by cell lineage reconstruction |
title | Distribution of neurosensory progenitor pools during inner ear morphogenesis unveiled by cell lineage reconstruction |
title_full | Distribution of neurosensory progenitor pools during inner ear morphogenesis unveiled by cell lineage reconstruction |
title_fullStr | Distribution of neurosensory progenitor pools during inner ear morphogenesis unveiled by cell lineage reconstruction |
title_full_unstemmed | Distribution of neurosensory progenitor pools during inner ear morphogenesis unveiled by cell lineage reconstruction |
title_short | Distribution of neurosensory progenitor pools during inner ear morphogenesis unveiled by cell lineage reconstruction |
title_sort | distribution of neurosensory progenitor pools during inner ear morphogenesis unveiled by cell lineage reconstruction |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5243114/ https://www.ncbi.nlm.nih.gov/pubmed/28051766 http://dx.doi.org/10.7554/eLife.22268 |
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