Therapeutic potential of induced neural stem cells for spinal cord injury

J Biol Chem. 2014 Nov 21;289(47):32512-25. doi: 10.1074/jbc.M114.588871. Epub 2014 Oct 6.

Abstract

The spinal cord does not spontaneously regenerate, and treatment that ensures functional recovery after spinal cord injury (SCI) is still not available. Recently, fibroblasts have been directly converted into induced neural stem cells (iNSCs) by the forced expression defined transcription factors. Although directly converted iNSCs have been considered to be a cell source for clinical applications, their therapeutic potential has not yet been investigated. Here we show that iNSCs directly converted from mouse fibroblasts enhance the functional recovery of SCI animals. Engrafted iNSCs could differentiate into all neuronal lineages, including different subtypes of mature neurons. Furthermore, iNSC-derived neurons could form synapses with host neurons, thus enhancing the locomotor function recovery. A time course analysis of iNSC-treated SCI animals revealed that engrafted iNSCs effectively reduced the inflammatory response and apoptosis in the injured area. iNSC transplantation also promoted the active regeneration of the endogenous recipient environment in the absence of tumor formation. Therefore, our data suggest that directly converted iNSCs hold therapeutic potential for treatment of SCI and may thus represent a promising cell source for transplantation therapy in patients with SCI.

Keywords: Differentiation; Neural Stem Cell (NSC); Reprogramming; Stem Cells; Transplantation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / genetics
  • Cell Differentiation / physiology
  • Cells, Cultured
  • Embryo, Mammalian / cytology
  • Evoked Potentials, Motor / genetics
  • Evoked Potentials, Motor / physiology
  • Female
  • Fibroblasts / metabolism
  • Gene Expression Profiling
  • Immunohistochemistry
  • Induced Pluripotent Stem Cells / metabolism
  • Induced Pluripotent Stem Cells / transplantation*
  • Mice, Inbred C3H
  • Microscopy, Fluorescence
  • Nerve Regeneration / genetics
  • Nerve Regeneration / physiology
  • Nestin / genetics
  • Nestin / metabolism
  • Neural Stem Cells / metabolism
  • Neural Stem Cells / transplantation*
  • Oligonucleotide Array Sequence Analysis
  • Rats, Sprague-Dawley
  • Recovery of Function / genetics
  • Recovery of Function / physiology
  • Reverse Transcriptase Polymerase Chain Reaction
  • SOXB1 Transcription Factors / genetics
  • SOXB1 Transcription Factors / metabolism
  • Spinal Cord Injuries / genetics
  • Spinal Cord Injuries / physiopathology*
  • Spinal Cord Injuries / therapy*
  • Synapses / metabolism
  • Synapses / physiology

Substances

  • Nestin
  • SOXB1 Transcription Factors

Associated data

  • GEO/GSE51331