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Blocking Notch-Signaling Increases Neurogenesis in the Striatum after Stroke

Stroke triggers neurogenesis in the striatum in mice, with new neurons deriving in part from the nearby subventricular zone and in part from parenchymal astrocytes. The initiation of neurogenesis by astrocytes within the striatum is triggered by reduced Notch-signaling, and blocking this signaling p...

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Autores principales: Santopolo, Giuseppe, Magnusson, Jens P., Lindvall, Olle, Kokaia, Zaal, Frisén, Jonas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409130/
https://www.ncbi.nlm.nih.gov/pubmed/32698472
http://dx.doi.org/10.3390/cells9071732
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author Santopolo, Giuseppe
Magnusson, Jens P.
Lindvall, Olle
Kokaia, Zaal
Frisén, Jonas
author_facet Santopolo, Giuseppe
Magnusson, Jens P.
Lindvall, Olle
Kokaia, Zaal
Frisén, Jonas
author_sort Santopolo, Giuseppe
collection PubMed
description Stroke triggers neurogenesis in the striatum in mice, with new neurons deriving in part from the nearby subventricular zone and in part from parenchymal astrocytes. The initiation of neurogenesis by astrocytes within the striatum is triggered by reduced Notch-signaling, and blocking this signaling pathway by deletion of the gene encoding the obligate Notch coactivator Rbpj is sufficient to activate neurogenesis by striatal astrocytes in the absence of an injury. Here we report that blocking Notch-signaling in stroke increases the neurogenic response to stroke 3.5-fold in mice. Deletion of Rbpj results in the recruitment of a larger number of parenchymal astrocytes to neurogenesis and over larger areas of the striatum. These data suggest inhibition of Notch-signaling as a potential translational strategy to promote neuronal regeneration after stroke.
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spelling pubmed-74091302020-08-26 Blocking Notch-Signaling Increases Neurogenesis in the Striatum after Stroke Santopolo, Giuseppe Magnusson, Jens P. Lindvall, Olle Kokaia, Zaal Frisén, Jonas Cells Communication Stroke triggers neurogenesis in the striatum in mice, with new neurons deriving in part from the nearby subventricular zone and in part from parenchymal astrocytes. The initiation of neurogenesis by astrocytes within the striatum is triggered by reduced Notch-signaling, and blocking this signaling pathway by deletion of the gene encoding the obligate Notch coactivator Rbpj is sufficient to activate neurogenesis by striatal astrocytes in the absence of an injury. Here we report that blocking Notch-signaling in stroke increases the neurogenic response to stroke 3.5-fold in mice. Deletion of Rbpj results in the recruitment of a larger number of parenchymal astrocytes to neurogenesis and over larger areas of the striatum. These data suggest inhibition of Notch-signaling as a potential translational strategy to promote neuronal regeneration after stroke. MDPI 2020-07-20 /pmc/articles/PMC7409130/ /pubmed/32698472 http://dx.doi.org/10.3390/cells9071732 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Santopolo, Giuseppe
Magnusson, Jens P.
Lindvall, Olle
Kokaia, Zaal
Frisén, Jonas
Blocking Notch-Signaling Increases Neurogenesis in the Striatum after Stroke
title Blocking Notch-Signaling Increases Neurogenesis in the Striatum after Stroke
title_full Blocking Notch-Signaling Increases Neurogenesis in the Striatum after Stroke
title_fullStr Blocking Notch-Signaling Increases Neurogenesis in the Striatum after Stroke
title_full_unstemmed Blocking Notch-Signaling Increases Neurogenesis in the Striatum after Stroke
title_short Blocking Notch-Signaling Increases Neurogenesis in the Striatum after Stroke
title_sort blocking notch-signaling increases neurogenesis in the striatum after stroke
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409130/
https://www.ncbi.nlm.nih.gov/pubmed/32698472
http://dx.doi.org/10.3390/cells9071732
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