Fine processes of Nestin-GFP-positive radial glia-like stem cells in the adult dentate gyrus ensheathe local synapses and vasculature

Proc Natl Acad Sci U S A. 2016 May 3;113(18):E2536-45. doi: 10.1073/pnas.1514652113. Epub 2016 Apr 18.

Abstract

Adult hippocampal neurogenesis relies on the activation of neural stem cells in the dentate gyrus, their division, and differentiation of their progeny into mature granule neurons. The complex morphology of radial glia-like (RGL) stem cells suggests that these cells establish numerous contacts with the cellular components of the neurogenic niche that may play a crucial role in the regulation of RGL stem cell activity. However, the morphology of RGL stem cells remains poorly described. Here, we used light microscopy and electron microscopy to examine Nestin-GFP transgenic mice and provide a detailed ultrastructural reconstruction analysis of Nestin-GFP-positive RGL cells of the dentate gyrus. We show that their primary processes follow a tortuous path from the subgranular zone through the granule cell layer and ensheathe local synapses and vasculature in the inner molecular layer. They share the ensheathing of synapses and vasculature with astrocytic processes and adhere to the adjacent processes of astrocytes. This extensive interaction of processes with their local environment could allow them to be uniquely receptive to signals from local neurons, glia, and vasculature, which may regulate their fate.

Keywords: adult neural stem cell; adult neurogenesis; electron microscopy; hippocampus; neurogenic niche.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astrocytes / cytology
  • Cells, Cultured
  • Cerebral Arteries / cytology*
  • Cerebral Arteries / metabolism
  • Dentate Gyrus / cytology*
  • Dentate Gyrus / metabolism
  • Green Fluorescent Proteins
  • Male
  • Mice
  • Mice, Transgenic
  • Nestin / metabolism*
  • Neural Stem Cells / cytology
  • Neural Stem Cells / metabolism
  • Neurogenesis / physiology
  • Neuroglia / cytology*
  • Neuroglia / metabolism*
  • Neurovascular Coupling / physiology
  • Stem Cell Niche / physiology
  • Synapses / metabolism
  • Synapses / ultrastructure*
  • Tissue Distribution

Substances

  • Nes protein, mouse
  • Nestin
  • Green Fluorescent Proteins