Multipotency of Adult Hippocampal NSCs In Vivo Is Restricted by Drosha/NFIB

Cell Stem Cell. 2016 Nov 3;19(5):653-662. doi: 10.1016/j.stem.2016.07.003. Epub 2016 Aug 18.

Abstract

Adult neural stem cells (NSCs) are defined by their inherent capacity to self-renew and give rise to neurons, astrocytes, and oligodendrocytes. In vivo, however, hippocampal NSCs do not generate oligodendrocytes for reasons that have remained enigmatic. Here, we report that deletion of Drosha in adult dentate gyrus NSCs activates oligodendrogenesis and reduces neurogenesis at the expense of gliogenesis. We further find that Drosha directly targets NFIB to repress its expression independently of Dicer and microRNAs. Knockdown of NFIB in Drosha-deficient hippocampal NSCs restores neurogenesis, suggesting that the Drosha/NFIB mechanism robustly prevents oligodendrocyte fate acquisition in vivo. Taken together, our findings establish that adult hippocampal NSCs inherently possess multilineage potential but that Drosha functions as a molecular barrier preventing oligodendrogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult Stem Cells / cytology*
  • Adult Stem Cells / metabolism
  • Aging / metabolism*
  • Animals
  • Base Sequence
  • Cell Differentiation
  • Dentate Gyrus / cytology
  • Gene Deletion
  • Gene Knockdown Techniques
  • Hippocampus / cytology*
  • Mice
  • Mice, Knockout
  • Multipotent Stem Cells / cytology*
  • Multipotent Stem Cells / metabolism
  • NFI Transcription Factors / genetics
  • NFI Transcription Factors / metabolism*
  • Neural Stem Cells / cytology*
  • Neural Stem Cells / metabolism
  • Neurogenesis / genetics
  • Oligodendroglia / cytology
  • Oligodendroglia / metabolism
  • Protein Binding
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Ribonuclease III / metabolism*

Substances

  • NFI Transcription Factors
  • Nfib protein, mouse
  • RNA, Messenger
  • Drosha protein, mouse
  • Ribonuclease III