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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2019
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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. |
format | Online Article Text |
id | pubmed-7375831 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
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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