Over-expression of Oct4 and Sox2 transcription factors enhances differentiation of human umbilical cord blood cells in vivo

Biochem Biophys Res Commun. 2014 Sep 5;451(4):503-9. doi: 10.1016/j.bbrc.2014.07.132. Epub 2014 Aug 11.

Abstract

Gene and cell-based therapies comprise innovative aspects of regenerative medicine. Even though stem cells represent a highly potential therapeutic strategy, their wide-spread exploitation is marred by ethical concerns, potential for malignant transformation and a plethora of other technical issues, largely restricting their use to experimental studies. Utilizing genetically modified human umbilical cord blood mono-nuclear cells (hUCB-MCs), this communication reports enhanced differentiation of transplants in a mouse model of amyotrophic lateral sclerosis (ALS). Over-expressing Oct4 and Sox2 induced production of neural marker PGP9.5, as well as transformation of hUCB-MCs into micro-glial and endothelial lines in ALS spinal cords. In addition to producing new nerve cells, providing degenerated areas with trophic factors and neo-vascularisation might prevent and even reverse progressive loss of moto-neurons and skeletal muscle paralysis.

Keywords: Amyotrophic lateral sclerosis; Differentiation; Pluripotency; Transcription factor; Umbilical cord blood mono-nuclear cell.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyotrophic Lateral Sclerosis / genetics
  • Animals
  • Cell Dedifferentiation
  • Cell Differentiation
  • Disease Models, Animal
  • Fetal Blood / cytology*
  • Humans
  • Mice
  • Octamer Transcription Factor-3 / biosynthesis*
  • Pluripotent Stem Cells / metabolism
  • Regenerative Medicine
  • SOXB1 Transcription Factors / biosynthesis*
  • Transfection

Substances

  • Octamer Transcription Factor-3
  • POU5F1 protein, human
  • SOX2 protein, human
  • SOXB1 Transcription Factors