Engrafted VHL peptide-delivered bone marrow stromal cells promote spinal cord repair in rats

Neuroreport. 2010 Mar 10;21(4):287-92. doi: 10.1097/WNR.0b013e328336ee9a.

Abstract

Stem cell-based therapy using bone marrow stromal cells (MSCs) has been expected to be a promising therapy for neuronal regeneration. To repair the injured spinal cord, neuronal differentiation of MSCs before transplantation has a more satisfactory effect. Recently, neuronal differentiation of neural progenitor/stem cells by an intracellular delivery of a pVHL-derived synthetic peptide (VHL peptide) has been shown. Here, we show that VHL peptide-delivered MSCs differentiated into neuron-like cells, and that engrafted VHL peptide-delivered MSCs more recovered the behaviors of the rats than that of nondelivered MSCs. Our result suggests that the use of VHL peptide-delivered MSCs would be a promising therapeutic strategy for repairing the injured spinal cord.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Blotting, Western
  • Bone Marrow Cells / cytology
  • Bone Marrow Cells / metabolism
  • Cell Culture Techniques
  • Cell Differentiation
  • Disease Models, Animal
  • Immunohistochemistry
  • Male
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / metabolism
  • Nerve Regeneration*
  • Neurofilament Proteins / genetics
  • Neurofilament Proteins / metabolism
  • Peptide Biosynthesis / genetics
  • Peptide Fragments / genetics
  • Peptide Fragments / metabolism
  • Peptide Fragments / pharmacology*
  • Rats
  • Rats, Wistar
  • Recombinant Fusion Proteins / chemical synthesis
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / pharmacology
  • Recovery of Function*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Spinal Cord Injuries / metabolism
  • Spinal Cord Injuries / physiopathology
  • Spinal Cord Injuries / surgery*
  • Stem Cell Transplantation / methods*
  • Stem Cells / cytology
  • Stem Cells / drug effects
  • Stem Cells / metabolism
  • Transduction, Genetic / methods
  • Von Hippel-Lindau Tumor Suppressor Protein / genetics
  • Von Hippel-Lindau Tumor Suppressor Protein / metabolism
  • Von Hippel-Lindau Tumor Suppressor Protein / pharmacology*

Substances

  • MAP2 protein, rat
  • Microtubule-Associated Proteins
  • Neurofilament Proteins
  • Peptide Fragments
  • Recombinant Fusion Proteins
  • neurofilament protein H
  • Von Hippel-Lindau Tumor Suppressor Protein