MicroRNA-153 Regulates the Acquisition of Gliogenic Competence by Neural Stem Cells

Stem Cell Reports. 2015 Sep 8;5(3):365-77. doi: 10.1016/j.stemcr.2015.06.006. Epub 2015 Jul 23.

Abstract

Mammalian neural stem/progenitor cells (NSPCs) sequentially generate neurons and glia during CNS development. Here we identified miRNA-153 (miR-153) as a modulator of the temporal regulation of NSPC differentiation. Overexpression (OE) of miR-153 delayed the onset of astrogliogenesis and maintained NSPCs in an undifferentiated state in vitro and in the developing cortex. The transcription factors nuclear factor I (NFI) A and B, essential regulators of the initiation of gliogenesis, were found to be targets of miR-153. Inhibition of miR-153 in early neurogenic NSPCs induced precocious gliogenesis, whereas NFIA/B overexpression rescued the anti-gliogenic phenotypes induced by miR-153 OE. Our results indicate that miR-mediated fine control of NFIA/B expression is important in the molecular networks that regulate the acquisition of gliogenic competence by NSPCs in the developing CNS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / physiology*
  • Cerebral Cortex / cytology
  • Cerebral Cortex / metabolism*
  • Mice
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • NFI Transcription Factors / genetics
  • NFI Transcription Factors / metabolism
  • Neural Stem Cells / cytology
  • Neural Stem Cells / metabolism*
  • Neuroglia / cytology
  • Neuroglia / metabolism*

Substances

  • MIRN153 microRNA, mouse
  • MicroRNAs
  • NFI Transcription Factors
  • Nfia protein, mouse
  • Nfib protein, mouse

Associated data

  • GEO/GSE70131