Lineage Reprogramming of Astroglial Cells from Different Origins into Distinct Neuronal Subtypes

Astroglial cells isolated from the rodent postnatal cerebral cortex are particularly susceptible to lineage reprogramming into neurons. However, it remains unknown whether other astroglial populations retain the same potential. Likewise, little is known about the fate of induced neurons (iNs) in viv...

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Main Authors: Malek Chouchane, Ana Raquel Melo de Farias, Daniela Maria de Sousa Moura, Markus Michael Hilscher, Timm Schroeder, Richardson Naves Leão, Marcos Romualdo Costa
Format: Article
Language:English
Published: Elsevier 2017-07-01
Series:Stem Cell Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2213671117302163
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author Malek Chouchane
Ana Raquel Melo de Farias
Daniela Maria de Sousa Moura
Markus Michael Hilscher
Timm Schroeder
Richardson Naves Leão
Marcos Romualdo Costa
author_facet Malek Chouchane
Ana Raquel Melo de Farias
Daniela Maria de Sousa Moura
Markus Michael Hilscher
Timm Schroeder
Richardson Naves Leão
Marcos Romualdo Costa
author_sort Malek Chouchane
collection DOAJ
description Astroglial cells isolated from the rodent postnatal cerebral cortex are particularly susceptible to lineage reprogramming into neurons. However, it remains unknown whether other astroglial populations retain the same potential. Likewise, little is known about the fate of induced neurons (iNs) in vivo. In this study we addressed these questions using two different astroglial populations isolated from the postnatal brain reprogrammed either with Neurogenin-2 (Neurog2) or Achaete scute homolog-1 (Ascl1). We show that cerebellum (CerebAstro) and cerebral cortex astroglia (CtxAstro) generates iNs with distinctive neurochemical and morphological properties. Both astroglial populations contribute iNs to the olfactory bulb following transplantation in the postnatal and adult mouse subventricular zone. However, only CtxAstro transfected with Neurog2 differentiate into pyramidal-like iNs after transplantation in the postnatal cerebral cortex. Altogether, our data indicate that the origin of the astroglial population and transcription factors used for reprogramming, as well as the region of integration, affect the fate of iNs.
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spelling doaj.art-10821dc38c664730af3aa2a4282c10ea2022-12-22T03:56:25ZengElsevierStem Cell Reports2213-67112017-07-019116217610.1016/j.stemcr.2017.05.009Lineage Reprogramming of Astroglial Cells from Different Origins into Distinct Neuronal SubtypesMalek Chouchane0Ana Raquel Melo de Farias1Daniela Maria de Sousa Moura2Markus Michael Hilscher3Timm Schroeder4Richardson Naves Leão5Marcos Romualdo Costa6Brain Institute, Federal University of Rio Grande do Norte, Natal 59056-450, BrazilBrain Institute, Federal University of Rio Grande do Norte, Natal 59056-450, BrazilBrain Institute, Federal University of Rio Grande do Norte, Natal 59056-450, BrazilBrain Institute, Federal University of Rio Grande do Norte, Natal 59056-450, BrazilDepartment of Biosystems Science and Engineering, ETH Zurich, Mattenstrasse 26, 4058 Basel, SwitzerlandBrain Institute, Federal University of Rio Grande do Norte, Natal 59056-450, BrazilBrain Institute, Federal University of Rio Grande do Norte, Natal 59056-450, BrazilAstroglial cells isolated from the rodent postnatal cerebral cortex are particularly susceptible to lineage reprogramming into neurons. However, it remains unknown whether other astroglial populations retain the same potential. Likewise, little is known about the fate of induced neurons (iNs) in vivo. In this study we addressed these questions using two different astroglial populations isolated from the postnatal brain reprogrammed either with Neurogenin-2 (Neurog2) or Achaete scute homolog-1 (Ascl1). We show that cerebellum (CerebAstro) and cerebral cortex astroglia (CtxAstro) generates iNs with distinctive neurochemical and morphological properties. Both astroglial populations contribute iNs to the olfactory bulb following transplantation in the postnatal and adult mouse subventricular zone. However, only CtxAstro transfected with Neurog2 differentiate into pyramidal-like iNs after transplantation in the postnatal cerebral cortex. Altogether, our data indicate that the origin of the astroglial population and transcription factors used for reprogramming, as well as the region of integration, affect the fate of iNs.http://www.sciencedirect.com/science/article/pii/S2213671117302163lineage reprogramminginduced neuronsproneural genesastroglial cellscerebral cortexcerebellumcell transplantation
spellingShingle Malek Chouchane
Ana Raquel Melo de Farias
Daniela Maria de Sousa Moura
Markus Michael Hilscher
Timm Schroeder
Richardson Naves Leão
Marcos Romualdo Costa
Lineage Reprogramming of Astroglial Cells from Different Origins into Distinct Neuronal Subtypes
Stem Cell Reports
lineage reprogramming
induced neurons
proneural genes
astroglial cells
cerebral cortex
cerebellum
cell transplantation
title Lineage Reprogramming of Astroglial Cells from Different Origins into Distinct Neuronal Subtypes
title_full Lineage Reprogramming of Astroglial Cells from Different Origins into Distinct Neuronal Subtypes
title_fullStr Lineage Reprogramming of Astroglial Cells from Different Origins into Distinct Neuronal Subtypes
title_full_unstemmed Lineage Reprogramming of Astroglial Cells from Different Origins into Distinct Neuronal Subtypes
title_short Lineage Reprogramming of Astroglial Cells from Different Origins into Distinct Neuronal Subtypes
title_sort lineage reprogramming of astroglial cells from different origins into distinct neuronal subtypes
topic lineage reprogramming
induced neurons
proneural genes
astroglial cells
cerebral cortex
cerebellum
cell transplantation
url http://www.sciencedirect.com/science/article/pii/S2213671117302163
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