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Pineal progenitors originate from a non-neural territory limited by FGF signalling

The embryonic development of the pineal organ, a neuroendocrine gland on top of the diencephalon, remains enigmatic. Classic fate-mapping studies suggested that pineal progenitors originate from the lateral border of the anterior neural plate. We show here, using gene expression and fate mapping/lin...

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Autores principales: Staudt, Nicole, Giger, Florence A., Fielding, Triona, Hutt, James A., Foucher, Isabelle, Snowden, Vicky, Hellich, Agathe, Kiecker, Clemens, Houart, Corinne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375831/
https://www.ncbi.nlm.nih.gov/pubmed/31754007
http://dx.doi.org/10.1242/dev.171405
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author Staudt, Nicole
Giger, Florence A.
Fielding, Triona
Hutt, James A.
Foucher, Isabelle
Snowden, Vicky
Hellich, Agathe
Kiecker, Clemens
Houart, Corinne
author_facet Staudt, Nicole
Giger, Florence A.
Fielding, Triona
Hutt, James A.
Foucher, Isabelle
Snowden, Vicky
Hellich, Agathe
Kiecker, Clemens
Houart, Corinne
author_sort Staudt, Nicole
collection PubMed
description The embryonic development of the pineal organ, a neuroendocrine gland on top of the diencephalon, remains enigmatic. Classic fate-mapping studies suggested that pineal progenitors originate from the lateral border of the anterior neural plate. We show here, using gene expression and fate mapping/lineage tracing in zebrafish, that pineal progenitors originate, at least in part, from the non-neural ectoderm. Gene expression in chick indicates that this non-neural origin of pineal progenitors is conserved in amniotes. Genetic repression of placodal, but not neural crest, cell fate results in pineal hypoplasia in zebrafish, while mis-expression of transcription factors known to specify placodal identity during gastrulation promotes the formation of ectopic pineal progenitors. We also demonstrate that fibroblast growth factors (FGFs) position the pineal progenitor domain within the non-neural border by repressing pineal fate and that the Otx transcription factors promote pinealogenesis by inhibiting this FGF activity. The non-neural origin of the pineal organ reveals an underlying similarity in the formation of the pineal and pituitary glands, and suggests that all CNS neuroendocrine organs may require a non-neural contribution to form neurosecretory cells.
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spelling pubmed-73758312020-07-30 Pineal progenitors originate from a non-neural territory limited by FGF signalling Staudt, Nicole Giger, Florence A. Fielding, Triona Hutt, James A. Foucher, Isabelle Snowden, Vicky Hellich, Agathe Kiecker, Clemens Houart, Corinne Development Research Article The embryonic development of the pineal organ, a neuroendocrine gland on top of the diencephalon, remains enigmatic. Classic fate-mapping studies suggested that pineal progenitors originate from the lateral border of the anterior neural plate. We show here, using gene expression and fate mapping/lineage tracing in zebrafish, that pineal progenitors originate, at least in part, from the non-neural ectoderm. Gene expression in chick indicates that this non-neural origin of pineal progenitors is conserved in amniotes. Genetic repression of placodal, but not neural crest, cell fate results in pineal hypoplasia in zebrafish, while mis-expression of transcription factors known to specify placodal identity during gastrulation promotes the formation of ectopic pineal progenitors. We also demonstrate that fibroblast growth factors (FGFs) position the pineal progenitor domain within the non-neural border by repressing pineal fate and that the Otx transcription factors promote pinealogenesis by inhibiting this FGF activity. The non-neural origin of the pineal organ reveals an underlying similarity in the formation of the pineal and pituitary glands, and suggests that all CNS neuroendocrine organs may require a non-neural contribution to form neurosecretory cells. The Company of Biologists Ltd 2019-11-21 /pmc/articles/PMC7375831/ /pubmed/31754007 http://dx.doi.org/10.1242/dev.171405 Text en © 2019. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Staudt, Nicole
Giger, Florence A.
Fielding, Triona
Hutt, James A.
Foucher, Isabelle
Snowden, Vicky
Hellich, Agathe
Kiecker, Clemens
Houart, Corinne
Pineal progenitors originate from a non-neural territory limited by FGF signalling
title Pineal progenitors originate from a non-neural territory limited by FGF signalling
title_full Pineal progenitors originate from a non-neural territory limited by FGF signalling
title_fullStr Pineal progenitors originate from a non-neural territory limited by FGF signalling
title_full_unstemmed Pineal progenitors originate from a non-neural territory limited by FGF signalling
title_short Pineal progenitors originate from a non-neural territory limited by FGF signalling
title_sort pineal progenitors originate from a non-neural territory limited by fgf signalling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375831/
https://www.ncbi.nlm.nih.gov/pubmed/31754007
http://dx.doi.org/10.1242/dev.171405
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