Divergence between Neuronal and Oligodendroglial Cell Fate, in Postnatal Brain Neural Stem Cells, Leads to Divergent Properties in Polymorphic In Vitro Assays

Two main stem cell pools exist in the postnatal mammalian brain that, although they share some “stemness” properties, also exhibit significant differences. Multipotent neural stem cells survive within specialized microenvironments, called niches, and they are vulnerable to ageing. Oligodendroglial l...

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Main Authors: Maria Anesti, Stavroula Magkafa, Efstathia Prantikou, Ilias Kazanis
Format: Article
Language:English
Published: MDPI AG 2022-05-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/11/11/1743
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author Maria Anesti
Stavroula Magkafa
Efstathia Prantikou
Ilias Kazanis
author_facet Maria Anesti
Stavroula Magkafa
Efstathia Prantikou
Ilias Kazanis
author_sort Maria Anesti
collection DOAJ
description Two main stem cell pools exist in the postnatal mammalian brain that, although they share some “stemness” properties, also exhibit significant differences. Multipotent neural stem cells survive within specialized microenvironments, called niches, and they are vulnerable to ageing. Oligodendroglial lineage-restricted progenitor cells are widely distributed in the brain parenchyma and are more resistant to the effects of ageing. Here, we create polymorphic neural stem cell cultures and allow cells to progress towards the neuronal and the oligodendroglial lineage. We show that the divergence of cell fate is accompanied by a divergence in the properties of progenitors, which reflects their adaptation to life in the niche or the parenchyma. Neurogenesis shows significant spatial restrictions and a dependence on laminin, a major niche component, while oligodendrogenesis shows none of these constraints. Furthermore, the blocking of integrin-β1 leads to opposing effects, reducing neurogenesis and enhancing oligodendrogenesis. Therefore, polymorphic neural stem cell assays can be used to investigate the divergence of postnatal brain stem cells and also to predict the in vivo effects of potential therapeutic molecules targeting stem and progenitor cells, as we do for the microneurotrophin BNN-20.
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spelling doaj.art-b7360f56d2604b9291d171ace11f3e742023-11-23T13:52:01ZengMDPI AGCells2073-44092022-05-011111174310.3390/cells11111743Divergence between Neuronal and Oligodendroglial Cell Fate, in Postnatal Brain Neural Stem Cells, Leads to Divergent Properties in Polymorphic In Vitro AssaysMaria Anesti0Stavroula Magkafa1Efstathia Prantikou2Ilias Kazanis3Laboratory of Developmental Biology, Department of Biology, University of Patras, 26504 Patras, GreeceLaboratory of Developmental Biology, Department of Biology, University of Patras, 26504 Patras, GreeceLaboratory of Developmental Biology, Department of Biology, University of Patras, 26504 Patras, GreeceLaboratory of Developmental Biology, Department of Biology, University of Patras, 26504 Patras, GreeceTwo main stem cell pools exist in the postnatal mammalian brain that, although they share some “stemness” properties, also exhibit significant differences. Multipotent neural stem cells survive within specialized microenvironments, called niches, and they are vulnerable to ageing. Oligodendroglial lineage-restricted progenitor cells are widely distributed in the brain parenchyma and are more resistant to the effects of ageing. Here, we create polymorphic neural stem cell cultures and allow cells to progress towards the neuronal and the oligodendroglial lineage. We show that the divergence of cell fate is accompanied by a divergence in the properties of progenitors, which reflects their adaptation to life in the niche or the parenchyma. Neurogenesis shows significant spatial restrictions and a dependence on laminin, a major niche component, while oligodendrogenesis shows none of these constraints. Furthermore, the blocking of integrin-β1 leads to opposing effects, reducing neurogenesis and enhancing oligodendrogenesis. Therefore, polymorphic neural stem cell assays can be used to investigate the divergence of postnatal brain stem cells and also to predict the in vivo effects of potential therapeutic molecules targeting stem and progenitor cells, as we do for the microneurotrophin BNN-20.https://www.mdpi.com/2073-4409/11/11/1743neural stem cellsoligodendrocyte progenitor cellsneurogenesisoligodendrogenesiscell fatemicroenvironment
spellingShingle Maria Anesti
Stavroula Magkafa
Efstathia Prantikou
Ilias Kazanis
Divergence between Neuronal and Oligodendroglial Cell Fate, in Postnatal Brain Neural Stem Cells, Leads to Divergent Properties in Polymorphic In Vitro Assays
Cells
neural stem cells
oligodendrocyte progenitor cells
neurogenesis
oligodendrogenesis
cell fate
microenvironment
title Divergence between Neuronal and Oligodendroglial Cell Fate, in Postnatal Brain Neural Stem Cells, Leads to Divergent Properties in Polymorphic In Vitro Assays
title_full Divergence between Neuronal and Oligodendroglial Cell Fate, in Postnatal Brain Neural Stem Cells, Leads to Divergent Properties in Polymorphic In Vitro Assays
title_fullStr Divergence between Neuronal and Oligodendroglial Cell Fate, in Postnatal Brain Neural Stem Cells, Leads to Divergent Properties in Polymorphic In Vitro Assays
title_full_unstemmed Divergence between Neuronal and Oligodendroglial Cell Fate, in Postnatal Brain Neural Stem Cells, Leads to Divergent Properties in Polymorphic In Vitro Assays
title_short Divergence between Neuronal and Oligodendroglial Cell Fate, in Postnatal Brain Neural Stem Cells, Leads to Divergent Properties in Polymorphic In Vitro Assays
title_sort divergence between neuronal and oligodendroglial cell fate in postnatal brain neural stem cells leads to divergent properties in polymorphic in vitro assays
topic neural stem cells
oligodendrocyte progenitor cells
neurogenesis
oligodendrogenesis
cell fate
microenvironment
url https://www.mdpi.com/2073-4409/11/11/1743
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