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Lineage Reprogramming of Astroglial Cells from Different Origins into Distinct Neuronal Subtypes.
- Source :
-
Stem cell reports [Stem Cell Reports] 2017 Jul 11; Vol. 9 (1), pp. 162-176. Date of Electronic Publication: 2017 Jun 08. - Publication Year :
- 2017
-
Abstract
- 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.<br /> (Copyright © 2017 The Authors. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Astrocytes metabolism
Basic Helix-Loop-Helix Transcription Factors genetics
Cell Lineage
Cells, Cultured
Cerebral Cortex cytology
Cerebral Cortex metabolism
Cerebral Cortex surgery
Mice
Nerve Tissue Proteins genetics
Neurons metabolism
Neurons transplantation
Transfection
Astrocytes cytology
Cellular Reprogramming
Neurons cytology
Subjects
Details
- Language :
- English
- ISSN :
- 2213-6711
- Volume :
- 9
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Stem cell reports
- Publication Type :
- Academic Journal
- Accession number :
- 28602612
- Full Text :
- https://doi.org/10.1016/j.stemcr.2017.05.009