Suppressor of fused controls perinatal expansion and quiescence of future dentate adult neural stem cells

Adult hippocampal neurogenesis requires the quiescent neural stem cell (NSC) pool to persist lifelong. However, establishment and maintenance of quiescent NSC pools during development is not understood. Here, we show that Suppressor of Fused (Sufu) controls establishment of the quiescent NSC pool du...

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Main Authors: Hirofumi Noguchi, Jesse Garcia Castillo, Kinichi Nakashima, Samuel J Pleasure
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2019-04-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/42918
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spelling doaj-bdf3dfc5a4e741fb9f61ba7e48df37292021-05-05T17:32:11ZengeLife Sciences Publications LtdeLife2050-084X2019-04-01810.7554/eLife.42918Suppressor of fused controls perinatal expansion and quiescence of future dentate adult neural stem cellsHirofumi Noguchi0https://orcid.org/0000-0002-9779-4956Jesse Garcia Castillo1Kinichi Nakashima2Samuel J Pleasure3https://orcid.org/0000-0001-8599-1613Department of Neurology, University of California, San Francisco, San Francisco, United StatesDepartment of Neurology, University of California, San Francisco, San Francisco, United StatesDepartment of Stem Cell Biology and Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, JapanPrograms in Neuroscience and Developmental Biology, Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, San Francisco, United StatesAdult hippocampal neurogenesis requires the quiescent neural stem cell (NSC) pool to persist lifelong. However, establishment and maintenance of quiescent NSC pools during development is not understood. Here, we show that Suppressor of Fused (Sufu) controls establishment of the quiescent NSC pool during mouse dentate gyrus (DG) development by regulating Sonic Hedgehog (Shh) signaling activity. Deletion of Sufu in NSCs early in DG development decreases Shh signaling activity leading to reduced proliferation of NSCs, resulting in a small quiescent NSC pool in adult mice. We found that putative adult NSCs proliferate and increase their numbers in the first postnatal week and subsequently enter a quiescent state towards the end of the first postnatal week. In the absence of Sufu, postnatal expansion of NSCs is compromised, and NSCs prematurely become quiescent. Thus, Sufu is required for Shh signaling activity ensuring expansion and proper transition of NSC pools to quiescent states during DG development.https://elifesciences.org/articles/42918stem celldentate gyrussonic hedgehoghippocampal development
collection DOAJ
language English
format Article
sources DOAJ
author Hirofumi Noguchi
Jesse Garcia Castillo
Kinichi Nakashima
Samuel J Pleasure
spellingShingle Hirofumi Noguchi
Jesse Garcia Castillo
Kinichi Nakashima
Samuel J Pleasure
Suppressor of fused controls perinatal expansion and quiescence of future dentate adult neural stem cells
eLife
stem cell
dentate gyrus
sonic hedgehog
hippocampal development
author_facet Hirofumi Noguchi
Jesse Garcia Castillo
Kinichi Nakashima
Samuel J Pleasure
author_sort Hirofumi Noguchi
title Suppressor of fused controls perinatal expansion and quiescence of future dentate adult neural stem cells
title_short Suppressor of fused controls perinatal expansion and quiescence of future dentate adult neural stem cells
title_full Suppressor of fused controls perinatal expansion and quiescence of future dentate adult neural stem cells
title_fullStr Suppressor of fused controls perinatal expansion and quiescence of future dentate adult neural stem cells
title_full_unstemmed Suppressor of fused controls perinatal expansion and quiescence of future dentate adult neural stem cells
title_sort suppressor of fused controls perinatal expansion and quiescence of future dentate adult neural stem cells
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2019-04-01
description Adult hippocampal neurogenesis requires the quiescent neural stem cell (NSC) pool to persist lifelong. However, establishment and maintenance of quiescent NSC pools during development is not understood. Here, we show that Suppressor of Fused (Sufu) controls establishment of the quiescent NSC pool during mouse dentate gyrus (DG) development by regulating Sonic Hedgehog (Shh) signaling activity. Deletion of Sufu in NSCs early in DG development decreases Shh signaling activity leading to reduced proliferation of NSCs, resulting in a small quiescent NSC pool in adult mice. We found that putative adult NSCs proliferate and increase their numbers in the first postnatal week and subsequently enter a quiescent state towards the end of the first postnatal week. In the absence of Sufu, postnatal expansion of NSCs is compromised, and NSCs prematurely become quiescent. Thus, Sufu is required for Shh signaling activity ensuring expansion and proper transition of NSC pools to quiescent states during DG development.
topic stem cell
dentate gyrus
sonic hedgehog
hippocampal development
url https://elifesciences.org/articles/42918
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