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Fgf10(+) progenitors give rise to the chick hypothalamus by rostral and caudal growth and differentiation
Classical descriptions of the hypothalamus divide it into three rostro-caudal domains but little is known about their embryonic origins. To investigate this, we performed targeted fate-mapping, molecular characterisation and cell cycle analyses in the embryonic chick. Presumptive hypothalamic cells...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5612254/ https://www.ncbi.nlm.nih.gov/pubmed/28807896 http://dx.doi.org/10.1242/dev.153379 |
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author | Fu, Travis Towers, Matthew Placzek, Marysia A. |
author_facet | Fu, Travis Towers, Matthew Placzek, Marysia A. |
author_sort | Fu, Travis |
collection | PubMed |
description | Classical descriptions of the hypothalamus divide it into three rostro-caudal domains but little is known about their embryonic origins. To investigate this, we performed targeted fate-mapping, molecular characterisation and cell cycle analyses in the embryonic chick. Presumptive hypothalamic cells derive from the rostral diencephalic ventral midline, lie above the prechordal mesendoderm and express Fgf10. Fgf10(+) progenitors undergo anisotropic growth: those displaced rostrally differentiate into anterior cells, then those displaced caudally differentiate into mammillary cells. A stable population of Fgf10(+) progenitors is retained within the tuberal domain; a subset of these gives rise to the tuberal infundibulum – the precursor of the posterior pituitary. Pharmacological approaches reveal that Shh signalling promotes the growth and differentiation of anterior progenitors, and also orchestrates the development of the infundibulum and Rathke's pouch – the precursor of the anterior pituitary. Together, our studies identify a hypothalamic progenitor population defined by Fgf10 and highlight a role for Shh signalling in the integrated development of the hypothalamus and pituitary. |
format | Online Article Text |
id | pubmed-5612254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-56122542017-10-06 Fgf10(+) progenitors give rise to the chick hypothalamus by rostral and caudal growth and differentiation Fu, Travis Towers, Matthew Placzek, Marysia A. Development Research Article Classical descriptions of the hypothalamus divide it into three rostro-caudal domains but little is known about their embryonic origins. To investigate this, we performed targeted fate-mapping, molecular characterisation and cell cycle analyses in the embryonic chick. Presumptive hypothalamic cells derive from the rostral diencephalic ventral midline, lie above the prechordal mesendoderm and express Fgf10. Fgf10(+) progenitors undergo anisotropic growth: those displaced rostrally differentiate into anterior cells, then those displaced caudally differentiate into mammillary cells. A stable population of Fgf10(+) progenitors is retained within the tuberal domain; a subset of these gives rise to the tuberal infundibulum – the precursor of the posterior pituitary. Pharmacological approaches reveal that Shh signalling promotes the growth and differentiation of anterior progenitors, and also orchestrates the development of the infundibulum and Rathke's pouch – the precursor of the anterior pituitary. Together, our studies identify a hypothalamic progenitor population defined by Fgf10 and highlight a role for Shh signalling in the integrated development of the hypothalamus and pituitary. The Company of Biologists Ltd 2017-09-15 /pmc/articles/PMC5612254/ /pubmed/28807896 http://dx.doi.org/10.1242/dev.153379 Text en © 2017. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Fu, Travis Towers, Matthew Placzek, Marysia A. Fgf10(+) progenitors give rise to the chick hypothalamus by rostral and caudal growth and differentiation |
title | Fgf10(+) progenitors give rise to the chick hypothalamus by rostral and caudal growth and differentiation |
title_full | Fgf10(+) progenitors give rise to the chick hypothalamus by rostral and caudal growth and differentiation |
title_fullStr | Fgf10(+) progenitors give rise to the chick hypothalamus by rostral and caudal growth and differentiation |
title_full_unstemmed | Fgf10(+) progenitors give rise to the chick hypothalamus by rostral and caudal growth and differentiation |
title_short | Fgf10(+) progenitors give rise to the chick hypothalamus by rostral and caudal growth and differentiation |
title_sort | fgf10(+) progenitors give rise to the chick hypothalamus by rostral and caudal growth and differentiation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5612254/ https://www.ncbi.nlm.nih.gov/pubmed/28807896 http://dx.doi.org/10.1242/dev.153379 |
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