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Ventricular–subventricular zone fractones are speckled basement membranes that function as a neural stem cell niche

Neural stem cells (NSCs) are retained in the adult ventricular–subventricular zone (V-SVZ), a specialized neurogenic niche with a unique cellular architecture. It currently remains unclear whether or how NSCs utilize basement membranes (BMs) in this niche. Here, we examine the molecular compositions...

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Autores principales: Sato, Yuya, Kiyozumi, Daiji, Futaki, Sugiko, Nakano, Itsuko, Shimono, Chisei, Kaneko, Naoko, Ikawa, Masahito, Okabe, Masaru, Sawamoto, Kazunobu, Sekiguchi, Kiyotoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337917/
https://www.ncbi.nlm.nih.gov/pubmed/30379609
http://dx.doi.org/10.1091/mbc.E18-05-0286
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author Sato, Yuya
Kiyozumi, Daiji
Futaki, Sugiko
Nakano, Itsuko
Shimono, Chisei
Kaneko, Naoko
Ikawa, Masahito
Okabe, Masaru
Sawamoto, Kazunobu
Sekiguchi, Kiyotoshi
author_facet Sato, Yuya
Kiyozumi, Daiji
Futaki, Sugiko
Nakano, Itsuko
Shimono, Chisei
Kaneko, Naoko
Ikawa, Masahito
Okabe, Masaru
Sawamoto, Kazunobu
Sekiguchi, Kiyotoshi
author_sort Sato, Yuya
collection PubMed
description Neural stem cells (NSCs) are retained in the adult ventricular–subventricular zone (V-SVZ), a specialized neurogenic niche with a unique cellular architecture. It currently remains unclear whether or how NSCs utilize basement membranes (BMs) in this niche. Here, we examine the molecular compositions and functions of BMs in the adult mouse V-SVZ. Whole-mount V-SVZ immunostaining revealed that fractones, which are fingerlike processes of extravascular BMs, are speckled BMs unconnected to the vasculature, and differ in their molecular composition from vascular BMs. Glial fibrillary acidic protein (GFAP)-positive astrocytes and NSCs produce and adhere to speckled BMs. Furthermore, Gfap-Cre-mediated Lamc1(flox(E1605Q)) knockin mice, in which integrin-binding activities of laminins are specifically nullified in GFAP-positive cells, exhibit a decreased number and size of speckled BMs and reduced in vitro neurosphere-forming activity. Our results reveal niche activities of fractones/speckled BMs for NSCs and provide molecular insights into how laminin–integrin interactions regulate NSCs in vivo.
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spelling pubmed-63379172019-03-16 Ventricular–subventricular zone fractones are speckled basement membranes that function as a neural stem cell niche Sato, Yuya Kiyozumi, Daiji Futaki, Sugiko Nakano, Itsuko Shimono, Chisei Kaneko, Naoko Ikawa, Masahito Okabe, Masaru Sawamoto, Kazunobu Sekiguchi, Kiyotoshi Mol Biol Cell Articles Neural stem cells (NSCs) are retained in the adult ventricular–subventricular zone (V-SVZ), a specialized neurogenic niche with a unique cellular architecture. It currently remains unclear whether or how NSCs utilize basement membranes (BMs) in this niche. Here, we examine the molecular compositions and functions of BMs in the adult mouse V-SVZ. Whole-mount V-SVZ immunostaining revealed that fractones, which are fingerlike processes of extravascular BMs, are speckled BMs unconnected to the vasculature, and differ in their molecular composition from vascular BMs. Glial fibrillary acidic protein (GFAP)-positive astrocytes and NSCs produce and adhere to speckled BMs. Furthermore, Gfap-Cre-mediated Lamc1(flox(E1605Q)) knockin mice, in which integrin-binding activities of laminins are specifically nullified in GFAP-positive cells, exhibit a decreased number and size of speckled BMs and reduced in vitro neurosphere-forming activity. Our results reveal niche activities of fractones/speckled BMs for NSCs and provide molecular insights into how laminin–integrin interactions regulate NSCs in vivo. The American Society for Cell Biology 2019-01-01 /pmc/articles/PMC6337917/ /pubmed/30379609 http://dx.doi.org/10.1091/mbc.E18-05-0286 Text en © 2019 Sato et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. http://creativecommons.org/licenses/by-nc-sa/3.0 This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License.
spellingShingle Articles
Sato, Yuya
Kiyozumi, Daiji
Futaki, Sugiko
Nakano, Itsuko
Shimono, Chisei
Kaneko, Naoko
Ikawa, Masahito
Okabe, Masaru
Sawamoto, Kazunobu
Sekiguchi, Kiyotoshi
Ventricular–subventricular zone fractones are speckled basement membranes that function as a neural stem cell niche
title Ventricular–subventricular zone fractones are speckled basement membranes that function as a neural stem cell niche
title_full Ventricular–subventricular zone fractones are speckled basement membranes that function as a neural stem cell niche
title_fullStr Ventricular–subventricular zone fractones are speckled basement membranes that function as a neural stem cell niche
title_full_unstemmed Ventricular–subventricular zone fractones are speckled basement membranes that function as a neural stem cell niche
title_short Ventricular–subventricular zone fractones are speckled basement membranes that function as a neural stem cell niche
title_sort ventricular–subventricular zone fractones are speckled basement membranes that function as a neural stem cell niche
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337917/
https://www.ncbi.nlm.nih.gov/pubmed/30379609
http://dx.doi.org/10.1091/mbc.E18-05-0286
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