Cargando…

Hedgehog Signaling Regulates Neurogenesis in the Larval and Adult Zebrafish Hypothalamus

Neurogenesis is now known to play a role in adult hypothalamic function, yet the cell-cell mechanisms regulating this neurogenesis remain poorly understood. Here, we show that Hedgehog (Hh)/Gli signaling positively regulates hypothalamic neurogenesis in both larval and adult zebrafish and is necessa...

Descripción completa

Detalles Bibliográficos
Autores principales: Male, Ira, Ozacar, A. Tuba, Fagan, Rita R., Loring, Matthew D., Shen, Meng-Chieh, Pace, Veronica A., Devine, Christine A., Lawson, Grace E., Lutservitz, Alyssa, Karlstrom, Rolf O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7769882/
https://www.ncbi.nlm.nih.gov/pubmed/33106384
http://dx.doi.org/10.1523/ENEURO.0226-20.2020
_version_ 1783629421991690240
author Male, Ira
Ozacar, A. Tuba
Fagan, Rita R.
Loring, Matthew D.
Shen, Meng-Chieh
Pace, Veronica A.
Devine, Christine A.
Lawson, Grace E.
Lutservitz, Alyssa
Karlstrom, Rolf O.
author_facet Male, Ira
Ozacar, A. Tuba
Fagan, Rita R.
Loring, Matthew D.
Shen, Meng-Chieh
Pace, Veronica A.
Devine, Christine A.
Lawson, Grace E.
Lutservitz, Alyssa
Karlstrom, Rolf O.
author_sort Male, Ira
collection PubMed
description Neurogenesis is now known to play a role in adult hypothalamic function, yet the cell-cell mechanisms regulating this neurogenesis remain poorly understood. Here, we show that Hedgehog (Hh)/Gli signaling positively regulates hypothalamic neurogenesis in both larval and adult zebrafish and is necessary and sufficient for normal hypothalamic proliferation rates. Hh-responsive radial glia represent a relatively highly proliferative precursor population that gives rise to dopaminergic, serotonergic, and GABAergic neurons. In situ and transgenic reporter analyses revealed substantial heterogeneity in cell-cell signaling within the hypothalamic niche, with slow cycling Nestin-expressing cells residing among distinct and overlapping populations of Sonic Hh (Shh)-expressing, Hh-responsive, Notch-responsive, and Wnt-responsive radial glia. This work shows for the first time that Hh/Gli signaling is a key component of the complex cell-cell signaling environment that regulates hypothalamic neurogenesis throughout life.
format Online
Article
Text
id pubmed-7769882
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Society for Neuroscience
record_format MEDLINE/PubMed
spelling pubmed-77698822020-12-29 Hedgehog Signaling Regulates Neurogenesis in the Larval and Adult Zebrafish Hypothalamus Male, Ira Ozacar, A. Tuba Fagan, Rita R. Loring, Matthew D. Shen, Meng-Chieh Pace, Veronica A. Devine, Christine A. Lawson, Grace E. Lutservitz, Alyssa Karlstrom, Rolf O. eNeuro Research Article: New Research Neurogenesis is now known to play a role in adult hypothalamic function, yet the cell-cell mechanisms regulating this neurogenesis remain poorly understood. Here, we show that Hedgehog (Hh)/Gli signaling positively regulates hypothalamic neurogenesis in both larval and adult zebrafish and is necessary and sufficient for normal hypothalamic proliferation rates. Hh-responsive radial glia represent a relatively highly proliferative precursor population that gives rise to dopaminergic, serotonergic, and GABAergic neurons. In situ and transgenic reporter analyses revealed substantial heterogeneity in cell-cell signaling within the hypothalamic niche, with slow cycling Nestin-expressing cells residing among distinct and overlapping populations of Sonic Hh (Shh)-expressing, Hh-responsive, Notch-responsive, and Wnt-responsive radial glia. This work shows for the first time that Hh/Gli signaling is a key component of the complex cell-cell signaling environment that regulates hypothalamic neurogenesis throughout life. Society for Neuroscience 2020-12-18 /pmc/articles/PMC7769882/ /pubmed/33106384 http://dx.doi.org/10.1523/ENEURO.0226-20.2020 Text en Copyright © 2020 Male et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://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: New Research
Male, Ira
Ozacar, A. Tuba
Fagan, Rita R.
Loring, Matthew D.
Shen, Meng-Chieh
Pace, Veronica A.
Devine, Christine A.
Lawson, Grace E.
Lutservitz, Alyssa
Karlstrom, Rolf O.
Hedgehog Signaling Regulates Neurogenesis in the Larval and Adult Zebrafish Hypothalamus
title Hedgehog Signaling Regulates Neurogenesis in the Larval and Adult Zebrafish Hypothalamus
title_full Hedgehog Signaling Regulates Neurogenesis in the Larval and Adult Zebrafish Hypothalamus
title_fullStr Hedgehog Signaling Regulates Neurogenesis in the Larval and Adult Zebrafish Hypothalamus
title_full_unstemmed Hedgehog Signaling Regulates Neurogenesis in the Larval and Adult Zebrafish Hypothalamus
title_short Hedgehog Signaling Regulates Neurogenesis in the Larval and Adult Zebrafish Hypothalamus
title_sort hedgehog signaling regulates neurogenesis in the larval and adult zebrafish hypothalamus
topic Research Article: New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7769882/
https://www.ncbi.nlm.nih.gov/pubmed/33106384
http://dx.doi.org/10.1523/ENEURO.0226-20.2020
work_keys_str_mv AT maleira hedgehogsignalingregulatesneurogenesisinthelarvalandadultzebrafishhypothalamus
AT ozacaratuba hedgehogsignalingregulatesneurogenesisinthelarvalandadultzebrafishhypothalamus
AT faganritar hedgehogsignalingregulatesneurogenesisinthelarvalandadultzebrafishhypothalamus
AT loringmatthewd hedgehogsignalingregulatesneurogenesisinthelarvalandadultzebrafishhypothalamus
AT shenmengchieh hedgehogsignalingregulatesneurogenesisinthelarvalandadultzebrafishhypothalamus
AT paceveronicaa hedgehogsignalingregulatesneurogenesisinthelarvalandadultzebrafishhypothalamus
AT devinechristinea hedgehogsignalingregulatesneurogenesisinthelarvalandadultzebrafishhypothalamus
AT lawsongracee hedgehogsignalingregulatesneurogenesisinthelarvalandadultzebrafishhypothalamus
AT lutservitzalyssa hedgehogsignalingregulatesneurogenesisinthelarvalandadultzebrafishhypothalamus
AT karlstromrolfo hedgehogsignalingregulatesneurogenesisinthelarvalandadultzebrafishhypothalamus