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Direct conversion of fibroblasts into functional astrocytes by defined transcription factors.
- Source :
-
Stem cell reports [Stem Cell Reports] 2015 Jan 13; Vol. 4 (1), pp. 25-36. Date of Electronic Publication: 2014 Dec 31. - Publication Year :
- 2015
-
Abstract
- Direct cell reprogramming enables direct conversion of fibroblasts into functional neurons and oligodendrocytes using a minimal set of cell-lineage-specific transcription factors. This approach is rapid and simple, generating the cell types of interest in one step. However, it remains unknown whether this technology can be applied to convert fibroblasts into astrocytes, the third neural lineage. Astrocytes play crucial roles in neuronal homeostasis, and their dysfunctions contribute to the origin and progression of multiple human diseases. Herein, we carried out a screening using several transcription factors involved in defining the astroglial cell fate and identified NFIA, NFIB, and SOX9 to be sufficient to convert with high efficiency embryonic and postnatal mouse fibroblasts into astrocytes (iAstrocytes). We proved both by gene-expression profiling and functional tests that iAstrocytes are comparable to native brain astrocytes. This protocol can be then employed to generate functional iAstrocytes for a wide range of experimental applications.<br /> (Copyright © 2015 The Authors. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Astrocytes drug effects
Biomarkers
Cell Transdifferentiation drug effects
Cells, Cultured
Cellular Reprogramming genetics
Cluster Analysis
Cytokines metabolism
Cytokines pharmacology
Fibroblasts drug effects
Gene Expression
Gene Expression Profiling
Humans
Membrane Potentials drug effects
Membrane Potentials genetics
Mice
Phenotype
Transcription Factors metabolism
Astrocytes cytology
Astrocytes metabolism
Cell Transdifferentiation genetics
Fibroblasts cytology
Fibroblasts metabolism
Transcription Factors genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2213-6711
- Volume :
- 4
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Stem cell reports
- Publication Type :
- Academic Journal
- Accession number :
- 25556566
- Full Text :
- https://doi.org/10.1016/j.stemcr.2014.12.002