Modeling the neurovascular niche: VEGF- and BDNF-mediated cross-talk between neural stem cells and endothelial cells: an in vitro study

J Neurosci Res. 2006 Dec;84(8):1656-68. doi: 10.1002/jnr.21087.

Abstract

Neural stem cells (NSCs) exist in vascularized niches. Although there has been ample evidence supporting a role for endothelial cell-derived soluble factors as modulators of neural stem cell self-renewal and neuronal differentiation there is a paucity of data reported on neural stem cell modulation of endothelial cell behavior. We show that co-culture of NSCs with brain-derived endothelial cells (BECs) either in direct contact or separated by a porous membrane elicited robust vascular tube formation and maintenance, mediated by induction of vascular vascular endothelial growth factor (VEGF) and brain-derived neurotrophic factor (BDNF) and activation of vascular VEGFR2 and TrkB by NSC NO. Nitric oxide (NO) scavengers and sequestration of VEGF and BDNF blunted this induction of tube formation, whereas addition of exogenous NO donor, rBDNF and rVEGF rescued the induction of tube formation. Further, rBDNF enhanced NSC eNOS activation and NO generation, suggesting an inducible positive feed-back signaling loop between NSCs and BECs, providing for homeostasis and responsiveness of the resident NSCs and BECs comprising the neurovascular niche. These findings show the importance of reciprocal modulation of NSCs and BECs in induction and maintenance of the neurovascular niche and underscores their dynamic interactions.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Analysis of Variance
  • Animals
  • Animals, Newborn
  • Brain / cytology
  • Brain-Derived Neurotrophic Factor / metabolism
  • Brain-Derived Neurotrophic Factor / pharmacology*
  • Cell Communication / drug effects*
  • Cell Communication / physiology
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Coculture Techniques / methods
  • Endothelial Cells / drug effects*
  • Endothelial Cells / physiology
  • Endothelial Cells / ultrastructure
  • Enzyme-Linked Immunosorbent Assay / methods
  • Green Fluorescent Proteins
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Microscopy, Electron, Transmission / methods
  • Models, Biological
  • Nerve Tissue Proteins / metabolism
  • Neurons / drug effects*
  • Neurons / physiology
  • Neurons / ultrastructure
  • Nitric Oxide / metabolism
  • Platelet Endothelial Cell Adhesion Molecule-1 / genetics
  • Stem Cells / drug effects*
  • Stem Cells / physiology
  • Vascular Endothelial Growth Factor A / metabolism
  • Vascular Endothelial Growth Factor A / pharmacology*

Substances

  • Brain-Derived Neurotrophic Factor
  • Nerve Tissue Proteins
  • Platelet Endothelial Cell Adhesion Molecule-1
  • Vascular Endothelial Growth Factor A
  • Green Fluorescent Proteins
  • Nitric Oxide