Wnt4-modified NSC transplantation promotes functional recovery after spinal cord injury

FASEB J. 2020 Jan;34(1):82-94. doi: 10.1096/fj.201901478RR. Epub 2019 Nov 19.

Abstract

Spinal cord injury (SCI) can lead to severe motor and sensory dysfunction, yet there are no effective therapies currently due to the failure of reconstructing the interruption of the neuroanatomical circuit. While neural stem cell (NSC) transplantation has been considered a potential strategy to repair the neural circuit after SCI, the efficacy of this strategy remains unproven. The main reason is that most of the transplanted NSC differentiates into astrocyte rather than neuron in the microenvironment of SCI. Our results demonstrated that Wnt4 significantly promotes the differentiation of NSC into neuron by activating both β-catenin and MAPK/JNK pathways and suppressing the activation of Notch signaling, which is acknowledged as prevention of NSC differentiation into neuron, through downregulating NICD expression, translocating and preventing the combination of NICD and RbpJ in nucleus. In addition, Wnt4 rescues the negative effect of Jagged, the ligand of Notch signaling, to promote neuronal differentiation. Moreover, in vivo study, transplantation of Wnt4-modified NSC efficaciously repairs the injured spinal cord and recovers the motor function of hind limbs after SCI. This study sheds new light into mechanisms that Wnt4-modified NSC transplantation is sufficient to repair the injured spinal cord and recover the motor dysfunction after SCI.

Keywords: Notch; Wnt; neural stem cell transplantation; neuronal differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Cell Differentiation
  • Female
  • Gene Expression Regulation
  • Lentivirus
  • Neural Stem Cells / transplantation*
  • Neurons
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Notch / genetics
  • Receptors, Notch / metabolism
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism
  • Signal Transduction
  • Spinal Cord Injuries / therapy*
  • Stem Cell Transplantation*
  • Transcription Factor HES-1 / genetics
  • Transcription Factor HES-1 / metabolism
  • Wnt4 Protein / metabolism*

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Hes1 protein, rat
  • Hes5 protein, rat
  • Receptors, Notch
  • Repressor Proteins
  • Transcription Factor HES-1
  • WNT4 protein, human
  • Wnt4 Protein