4.2 Article Proceedings Paper

Development of the basal hypothalamus through anisotropic growth

Journal

JOURNAL OF NEUROENDOCRINOLOGY
Volume 31, Issue 5, Pages -

Publisher

WILEY
DOI: 10.1111/jne.12727

Keywords

anisotropic growth; development; Fgf10; hypothalamus; prechordal mesendoderm; progenitor; sonic hedgehog

Funding

  1. Wellcome Trust [156548]

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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.

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