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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...

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Autores principales: Dyballa, Sylvia, Savy, Thierry, Germann, Philipp, Mikula, Karol, Remesikova, Mariana, Špir, Róbert, Zecca, Andrea, Peyriéras, Nadine, Pujades, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
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
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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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