Heterogeneous Expression of SDF1 Retains Actively Proliferating Neural Progenitors in the Capillary Compartment of the Niche

Stem Cell Reports. 2019 Jan 8;12(1):6-13. doi: 10.1016/j.stemcr.2018.11.022. Epub 2018 Dec 27.

Abstract

The vascular compartment of the adult brain ventricular-subventricular zone (V-SVZ) is a critical regulator of neural stem cell and progenitor function. Blood enters the V-SVZ via arteries and arterioles to capillaries that then connect with venules and veins to return blood to the heart. We found that stromal cell-derived factor 1 (SDF1) is expressed by a subpopulation of V-SVZ vessels, the capillaries, and that actively proliferating neural stem cells (NSCs) and progenitors are preferentially associated with these SDF1-positive vessels. In contrast, slowly dividing or quiescent NSCs are most prevalent near SDF1-negative vessels. By conditional knockout, we found that loss of SDF1 signaling in NSCs stimulates lineage progression and NSC displacement from the vessel niche. With aging, SDF1/CXCR4 signaling is dysregulated, coincident with reduced proliferation and increased displacement of dividing cells from the vasculature. Our findings demonstrate SDF1-based vascular heterogeneity in the niche and suggest that reduced SDF1 signaling contributes to age-related declines in adult neurogenesis.

Keywords: CXCL14; CXCR4; SDF1; blood vessels; neural stem cells; niche; vasculature.

Publication types

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

MeSH terms

  • Animals
  • Capillaries / cytology
  • Capillaries / metabolism*
  • Cell Proliferation
  • Chemokine CXCL12 / genetics*
  • Chemokine CXCL12 / metabolism
  • Lateral Ventricles / blood supply
  • Lateral Ventricles / cytology*
  • Lateral Ventricles / growth & development
  • Mice
  • Neural Stem Cells / cytology
  • Neural Stem Cells / metabolism*
  • Neural Stem Cells / physiology
  • Neurogenesis*
  • Receptors, CXCR4 / metabolism
  • Signal Transduction
  • Stem Cell Niche*

Substances

  • CXCR4 protein, mouse
  • Chemokine CXCL12
  • Cxcl12 protein, mouse
  • Receptors, CXCR4