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A novel stem cell type at the basal side of the subventricular zone maintains adult neurogenesis

According to the current consensus, murine neural stem cells (NSCs) apically contacting the lateral ventricle generate differentiated progenitors by rare asymmetric divisions or by relocating to the basal side of the ventricular–subventricular zone (V‐SVZ). Both processes will ultimately lead to the...

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Autores principales: Baur, Katja, Abdullah, Yomn, Mandl, Claudia, Hölzl‐Wenig, Gabriele, Shi, Yan, Edelkraut, Udo, Khatri, Priti, Hagenston, Anna M, Irmler, Martin, Beckers, Johannes, Ciccolini, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9442324/
https://www.ncbi.nlm.nih.gov/pubmed/35861333
http://dx.doi.org/10.15252/embr.202154078
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author Baur, Katja
Abdullah, Yomn
Mandl, Claudia
Hölzl‐Wenig, Gabriele
Shi, Yan
Edelkraut, Udo
Khatri, Priti
Hagenston, Anna M
Irmler, Martin
Beckers, Johannes
Ciccolini, Francesca
author_facet Baur, Katja
Abdullah, Yomn
Mandl, Claudia
Hölzl‐Wenig, Gabriele
Shi, Yan
Edelkraut, Udo
Khatri, Priti
Hagenston, Anna M
Irmler, Martin
Beckers, Johannes
Ciccolini, Francesca
author_sort Baur, Katja
collection PubMed
description According to the current consensus, murine neural stem cells (NSCs) apically contacting the lateral ventricle generate differentiated progenitors by rare asymmetric divisions or by relocating to the basal side of the ventricular–subventricular zone (V‐SVZ). Both processes will ultimately lead to the generation of adult‐born olfactory bulb (OB) interneurons. In contrast to this view, we here find that adult‐born OB interneurons largely derive from an additional NSC‐type resident in the basal V‐SVZ. Despite being both capable of self‐renewal and long‐term quiescence, apical and basal NSCs differ in Nestin expression, primary cilia extension and frequency of cell division. The expression of Notch‐related genes also differs between the two NSC groups, and Notch activation is greatest in apical NSCs. Apical downregulation of Notch‐effector Hes1 decreases Notch activation while increasing proliferation across the niche and neurogenesis from apical NSCs. Underscoring their different roles in neurogenesis, lactation‐dependent increase in neurogenesis is paralleled by extra activation of basal but not apical NSCs. Thus, basal NSCs support OB neurogenesis, whereas apical NSCs impart Notch‐mediated lateral inhibition across the V‐SVZ.
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spelling pubmed-94423242022-09-09 A novel stem cell type at the basal side of the subventricular zone maintains adult neurogenesis Baur, Katja Abdullah, Yomn Mandl, Claudia Hölzl‐Wenig, Gabriele Shi, Yan Edelkraut, Udo Khatri, Priti Hagenston, Anna M Irmler, Martin Beckers, Johannes Ciccolini, Francesca EMBO Rep Articles According to the current consensus, murine neural stem cells (NSCs) apically contacting the lateral ventricle generate differentiated progenitors by rare asymmetric divisions or by relocating to the basal side of the ventricular–subventricular zone (V‐SVZ). Both processes will ultimately lead to the generation of adult‐born olfactory bulb (OB) interneurons. In contrast to this view, we here find that adult‐born OB interneurons largely derive from an additional NSC‐type resident in the basal V‐SVZ. Despite being both capable of self‐renewal and long‐term quiescence, apical and basal NSCs differ in Nestin expression, primary cilia extension and frequency of cell division. The expression of Notch‐related genes also differs between the two NSC groups, and Notch activation is greatest in apical NSCs. Apical downregulation of Notch‐effector Hes1 decreases Notch activation while increasing proliferation across the niche and neurogenesis from apical NSCs. Underscoring their different roles in neurogenesis, lactation‐dependent increase in neurogenesis is paralleled by extra activation of basal but not apical NSCs. Thus, basal NSCs support OB neurogenesis, whereas apical NSCs impart Notch‐mediated lateral inhibition across the V‐SVZ. John Wiley and Sons Inc. 2022-07-21 /pmc/articles/PMC9442324/ /pubmed/35861333 http://dx.doi.org/10.15252/embr.202154078 Text en © 2022 The Authors. Published under the terms of the CC BY NC ND 4.0 license. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Articles
Baur, Katja
Abdullah, Yomn
Mandl, Claudia
Hölzl‐Wenig, Gabriele
Shi, Yan
Edelkraut, Udo
Khatri, Priti
Hagenston, Anna M
Irmler, Martin
Beckers, Johannes
Ciccolini, Francesca
A novel stem cell type at the basal side of the subventricular zone maintains adult neurogenesis
title A novel stem cell type at the basal side of the subventricular zone maintains adult neurogenesis
title_full A novel stem cell type at the basal side of the subventricular zone maintains adult neurogenesis
title_fullStr A novel stem cell type at the basal side of the subventricular zone maintains adult neurogenesis
title_full_unstemmed A novel stem cell type at the basal side of the subventricular zone maintains adult neurogenesis
title_short A novel stem cell type at the basal side of the subventricular zone maintains adult neurogenesis
title_sort novel stem cell type at the basal side of the subventricular zone maintains adult neurogenesis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9442324/
https://www.ncbi.nlm.nih.gov/pubmed/35861333
http://dx.doi.org/10.15252/embr.202154078
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