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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2019
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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. |
format | Online Article Text |
id | pubmed-6337917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
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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