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Development of the basal hypothalamus through anisotropic growth
The adult hypothalamus is subdivided into distinct domains: pre‐optic, anterior, tuberal and mammillary. Each domain harbours an array of neurones that act together to regulate homeostasis. The embryonic origins and the development of hypothalamic neurones, however, remain enigmatic. Here, we summar...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6563594/ https://www.ncbi.nlm.nih.gov/pubmed/31050853 http://dx.doi.org/10.1111/jne.12727 |
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author | Fu, Travis Pearson, Caroline Towers, Matthew Placzek, Marysia |
author_facet | Fu, Travis Pearson, Caroline Towers, Matthew Placzek, Marysia |
author_sort | Fu, Travis |
collection | PubMed |
description | The adult hypothalamus is subdivided into distinct domains: pre‐optic, anterior, tuberal and mammillary. Each domain harbours an array of neurones that act together to regulate homeostasis. The embryonic origins and the development of hypothalamic neurones, however, remain enigmatic. Here, we summarise recent studies in model organisms that challenge current views of hypothalamic development, which traditionally have attempted to map adult domains to correspondingly located embryonic domains. Instead, new studies indicate that hypothalamic neurones arise from progenitor cells that undergo anisotropic growth, expanding to a greater extent than other progenitors, and grow in different dimensions. We describe in particular how a multipotent Shh (/) Fgf10‐expressing progenitor population gives rise to progenitors throughout the basal hypothalamus that grow anisotropically and sequentially: first, a subset displaced rostrally give rise to anterior‐ventral/tuberal neuronal progenitors; then a subset displaced caudally give rise to mammillary neuronal progenitors; and, finally, a subset(s) displaced ventrally give rise to tuberal infundibular glial progenitors. As this occurs, stable populations of Shh (+ive) and Fgf10 (+ive) progenitors form. We describe current understanding of the mechanisms that induce Shh (+ive) /Fgf10 (+ive) progenitors and begin to direct their differentiation to anterior‐ventral/tuberal neuronal progenitors, mammillary neuronal progenitors and tuberal infundibular progenitors. Taken together, these studies suggest a new model for hypothalamic development that we term the “anisotropic growth model”. We discuss the implications of the model for understanding the origins of adult hypothalamic neurones. |
format | Online Article Text |
id | pubmed-6563594 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65635942019-06-20 Development of the basal hypothalamus through anisotropic growth Fu, Travis Pearson, Caroline Towers, Matthew Placzek, Marysia J Neuroendocrinol Review Articles The adult hypothalamus is subdivided into distinct domains: pre‐optic, anterior, tuberal and mammillary. Each domain harbours an array of neurones that act together to regulate homeostasis. The embryonic origins and the development of hypothalamic neurones, however, remain enigmatic. Here, we summarise recent studies in model organisms that challenge current views of hypothalamic development, which traditionally have attempted to map adult domains to correspondingly located embryonic domains. Instead, new studies indicate that hypothalamic neurones arise from progenitor cells that undergo anisotropic growth, expanding to a greater extent than other progenitors, and grow in different dimensions. We describe in particular how a multipotent Shh (/) Fgf10‐expressing progenitor population gives rise to progenitors throughout the basal hypothalamus that grow anisotropically and sequentially: first, a subset displaced rostrally give rise to anterior‐ventral/tuberal neuronal progenitors; then a subset displaced caudally give rise to mammillary neuronal progenitors; and, finally, a subset(s) displaced ventrally give rise to tuberal infundibular glial progenitors. As this occurs, stable populations of Shh (+ive) and Fgf10 (+ive) progenitors form. We describe current understanding of the mechanisms that induce Shh (+ive) /Fgf10 (+ive) progenitors and begin to direct their differentiation to anterior‐ventral/tuberal neuronal progenitors, mammillary neuronal progenitors and tuberal infundibular progenitors. Taken together, these studies suggest a new model for hypothalamic development that we term the “anisotropic growth model”. We discuss the implications of the model for understanding the origins of adult hypothalamic neurones. John Wiley and Sons Inc. 2019-05-23 2019-05 /pmc/articles/PMC6563594/ /pubmed/31050853 http://dx.doi.org/10.1111/jne.12727 Text en © 2019 The Authors. Journal of Neuroendocrinology published by John Wiley & Sons Ltd on behalf of British Society for Neuroendocrinology This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Articles Fu, Travis Pearson, Caroline Towers, Matthew Placzek, Marysia Development of the basal hypothalamus through anisotropic growth |
title | Development of the basal hypothalamus through anisotropic growth |
title_full | Development of the basal hypothalamus through anisotropic growth |
title_fullStr | Development of the basal hypothalamus through anisotropic growth |
title_full_unstemmed | Development of the basal hypothalamus through anisotropic growth |
title_short | Development of the basal hypothalamus through anisotropic growth |
title_sort | development of the basal hypothalamus through anisotropic growth |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6563594/ https://www.ncbi.nlm.nih.gov/pubmed/31050853 http://dx.doi.org/10.1111/jne.12727 |
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