PRDX6 Promotes the Differentiation of Human Mesenchymal Stem (Stromal) Cells to Insulin-Producing Cells

Biomed Res Int. 2020 Jan 21:2020:7103053. doi: 10.1155/2020/7103053. eCollection 2020.

Abstract

Mesenchymal stem cells (MSCs) can be differentiated in vitro to form insulin-producing cells (IPCs). However, the proportion of induced cells is modest. Extracts from injured pancreata of rodents promoted this differentiation, and three upregulated proteins were identified in these extracts. The aim of this study was to evaluate the potential benefits of adding these proteins to the differentiation medium alone or in combination. Our results indicate that the proportion of IPCs among the protein(s)-supplemented samples was significantly higher than that in the samples with no added proteins. The yield from samples supplemented with PRDX6 alone was 4-fold higher than that from samples without added protein. These findings were also supported by the results of fluorophotometry. Gene expression profiles revealed higher levels among protein-supplemented samples. Significantly higher levels of GGT, SST, Glut-2, and MafB expression were noted among PRDX6-treated samples. There was a stepwise increase in the release of insulin and c-peptide, as a function of increasing glucose concentrations, indicating that the differentiated cells were glucose sensitive and insulin responsive. PRDX6 exerts its beneficial effects as a result of its biological antioxidant properties. Considering its ease of use as a single protein, PRDX6 is now routinely used in our differentiation protocols.

MeSH terms

  • C-Peptide / metabolism
  • Cell Differentiation / drug effects*
  • Glucose / metabolism
  • Glucose Transporter Type 2 / metabolism
  • Humans
  • Insulin / biosynthesis*
  • MafB Transcription Factor / metabolism
  • Mesenchymal Stem Cells / metabolism*
  • Peroxiredoxin VI / genetics
  • Peroxiredoxin VI / metabolism*
  • Peroxiredoxin VI / pharmacology*
  • Somatostatin / metabolism
  • Transcriptome
  • gamma-Glutamyltransferase / metabolism

Substances

  • C-Peptide
  • Glucose Transporter Type 2
  • Insulin
  • MAFB protein, human
  • MafB Transcription Factor
  • SLC2A2 protein, human
  • SST protein, human
  • Somatostatin
  • PRDX6 protein, human
  • Peroxiredoxin VI
  • gamma-Glutamyltransferase
  • gamma-glutamyltransferase, human
  • Glucose