Rescue of Brain Function Using Tunneling Nanotubes Between Neural Stem Cells and Brain Microvascular Endothelial Cells

Mol Neurobiol. 2016 May;53(4):2480-8. doi: 10.1007/s12035-015-9225-z. Epub 2015 Jun 4.

Abstract

Evidence indicates that neural stem cells (NSCs) can ameliorate cerebral ischemia in animal models. In this study, we investigated the mechanism underlying one of the neuroprotective effects of NSCs: tunneling nanotube (TNT) formation. We addressed whether the control of cell-to-cell communication processes between NSCs and brain microvascular endothelial cells (BMECs) and, particularly, the control of TNT formation could influence the rescue function of stem cells. In an attempt to mimic the cellular microenvironment in vitro, a co-culture system consisting of terminally differentiated BMECs from mice in a distressed state and NSCs was constructed. Additionally, engraftment experiments with infarcted mouse brains revealed that control of TNT formation influenced the effects of stem cell transplantation in vivo. In conclusion, our findings provide the first evidence that TNTs exist between NSCs and BMECs and that regulation of TNT formation alters cell function.

Keywords: Brain microvascular endothelial cells; MCAO model; Neural stem cells; Tunneling nanotubes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Blotting, Western
  • Brain / blood supply*
  • Brain / physiology*
  • Endothelial Cells / cytology*
  • Endothelial Cells / drug effects
  • Infarction, Middle Cerebral Artery / pathology
  • Male
  • Mice, Inbred C57BL
  • Microvessels / cytology*
  • Nanotubes / chemistry*
  • Nanotubes / ultrastructure
  • Neural Stem Cells / cytology*
  • Neural Stem Cells / drug effects
  • Neural Stem Cells / ultrastructure
  • Nocodazole / pharmacology
  • Reactive Oxygen Species / metabolism
  • Staining and Labeling

Substances

  • Antioxidants
  • Reactive Oxygen Species
  • Nocodazole