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Non-canonical Wnt signaling regulates neural stem cell quiescence during homeostasis and after demyelination

Adult neural stem cells (NSCs) reside in a specialized microenvironment, the subventricular zone (SVZ), which provides them with unique signaling cues to control their basic properties and prevent their exhaustion. While the signaling mechanisms that regulate NSC lineage progression are well charact...

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Autores principales: Chavali, Manideep, Klingener, Michael, Kokkosis, Alexandros G., Garkun, Yury, Felong, Sylwia, Maffei, Arianna, Aguirre, Adan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5750230/
https://www.ncbi.nlm.nih.gov/pubmed/29296000
http://dx.doi.org/10.1038/s41467-017-02440-0
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author Chavali, Manideep
Klingener, Michael
Kokkosis, Alexandros G.
Garkun, Yury
Felong, Sylwia
Maffei, Arianna
Aguirre, Adan
author_facet Chavali, Manideep
Klingener, Michael
Kokkosis, Alexandros G.
Garkun, Yury
Felong, Sylwia
Maffei, Arianna
Aguirre, Adan
author_sort Chavali, Manideep
collection PubMed
description Adult neural stem cells (NSCs) reside in a specialized microenvironment, the subventricular zone (SVZ), which provides them with unique signaling cues to control their basic properties and prevent their exhaustion. While the signaling mechanisms that regulate NSC lineage progression are well characterized, the molecular mechanisms that trigger the activation of quiescent NSCs during homeostasis and tissue repair are still unclear. Here, we uncovered that the NSC quiescent state is maintained by Rho-GTPase Cdc42, a downstream target of non-canonical Wnt signaling. Mechanistically, activation of Cdc42 induces expression of molecules involved in stem cell identity and anchorage to the niche. Strikingly, during a demyelination injury, downregulation of non-canonical Wnt-dependent Cdc42 activity is necessary to promote activation and lineage progression of quiescent NSCs, thereby initiating the process of tissue repair.
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spelling pubmed-57502302018-01-13 Non-canonical Wnt signaling regulates neural stem cell quiescence during homeostasis and after demyelination Chavali, Manideep Klingener, Michael Kokkosis, Alexandros G. Garkun, Yury Felong, Sylwia Maffei, Arianna Aguirre, Adan Nat Commun Article Adult neural stem cells (NSCs) reside in a specialized microenvironment, the subventricular zone (SVZ), which provides them with unique signaling cues to control their basic properties and prevent their exhaustion. While the signaling mechanisms that regulate NSC lineage progression are well characterized, the molecular mechanisms that trigger the activation of quiescent NSCs during homeostasis and tissue repair are still unclear. Here, we uncovered that the NSC quiescent state is maintained by Rho-GTPase Cdc42, a downstream target of non-canonical Wnt signaling. Mechanistically, activation of Cdc42 induces expression of molecules involved in stem cell identity and anchorage to the niche. Strikingly, during a demyelination injury, downregulation of non-canonical Wnt-dependent Cdc42 activity is necessary to promote activation and lineage progression of quiescent NSCs, thereby initiating the process of tissue repair. Nature Publishing Group UK 2018-01-02 /pmc/articles/PMC5750230/ /pubmed/29296000 http://dx.doi.org/10.1038/s41467-017-02440-0 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chavali, Manideep
Klingener, Michael
Kokkosis, Alexandros G.
Garkun, Yury
Felong, Sylwia
Maffei, Arianna
Aguirre, Adan
Non-canonical Wnt signaling regulates neural stem cell quiescence during homeostasis and after demyelination
title Non-canonical Wnt signaling regulates neural stem cell quiescence during homeostasis and after demyelination
title_full Non-canonical Wnt signaling regulates neural stem cell quiescence during homeostasis and after demyelination
title_fullStr Non-canonical Wnt signaling regulates neural stem cell quiescence during homeostasis and after demyelination
title_full_unstemmed Non-canonical Wnt signaling regulates neural stem cell quiescence during homeostasis and after demyelination
title_short Non-canonical Wnt signaling regulates neural stem cell quiescence during homeostasis and after demyelination
title_sort non-canonical wnt signaling regulates neural stem cell quiescence during homeostasis and after demyelination
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5750230/
https://www.ncbi.nlm.nih.gov/pubmed/29296000
http://dx.doi.org/10.1038/s41467-017-02440-0
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