Vascular endothelial growth factor activates neural stem cells through epidermal growth factor receptor signal after spinal cord injury

CNS Neurosci Ther. 2019 Mar;25(3):375-385. doi: 10.1111/cns.13056. Epub 2018 Aug 29.

Abstract

Aims: Neural stem cells (NSCs) in the adult mammalian spinal cord are activated in response to spinal cord injury (SCI); however, mechanisms modulating this process are not clear. Here, we noticed SCI elevated expression of vascular endothelial growth factor (VEGF) and we aimed to validate the roles of VEGF in NSCs activation after SCI and investigated the related signals during the process.

Methods: In vitro we detected whether VEGF promoted spinal cord NSCs proliferation and investigated the involved signals; In vivo, we injected VEGF into rat spinal cord to check the NSCs activation.

Results: In vitro, VEGF triggered spinal cord NSCs proliferation and maintained self-renewal. Further investigations demonstrated VEGF transactivated epidermal growth factor receptor (EGFR) through VEGF receptor 2 (VEGFR2) to promote spinal cord NSCs proliferation. In vivo, we injected VEGF into spinal cord by laminectomy to confirm the roles of VEGF-VEGFR2-EGFR signals in NSCs activation. VEGF significantly elevated the number of activated NSCs and increased EGFR phosphorylation. In contrast, intraspinal injection of specific inhibitors targeting EGFR and VEGFR2 decreased NSCs activation after SCI. Our results demonstrate that VEGF-VEGFR2-EGFR axis is important for NSCs activation after SCI, providing new insights into the mechanisms of spinal cord NSCs activation postinjury.

Keywords: VEGF receptor 2; epidermal growth factor receptor; neural stem cells activation; spinal cord injury; vascular endothelial growth factor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Proliferation / physiology
  • Cells, Cultured
  • Disease Models, Animal
  • ErbB Receptors / metabolism*
  • Female
  • Neural Stem Cells / metabolism*
  • Rats, Sprague-Dawley
  • Signal Transduction
  • Spinal Cord / metabolism
  • Spinal Cord Injuries / metabolism*
  • Vascular Endothelial Growth Factor A / metabolism*
  • Vascular Endothelial Growth Factor Receptor-2 / metabolism

Substances

  • Vascular Endothelial Growth Factor A
  • vascular endothelial growth factor A, rat
  • ErbB Receptors
  • Vascular Endothelial Growth Factor Receptor-2