MicroRNA-191 regulates differentiation and migration of mesenchymal stem cells and their paracrine effect on angiogenesis

Biotechnol Lett. 2020 Sep;42(9):1777-1788. doi: 10.1007/s10529-020-02907-z. Epub 2020 May 20.

Abstract

MicroRNAs (miRNAs) are critical regulators in organ development. Among them, miR-191 is known to be regulated in early embryogenesis and dysregulated in cancer. This role in undifferentiated tissues suggests a possible part of miR-191 also in bone marrow derived mesenchymal stem cells (BMSCs) physiology. Here, we report that miR-191 decreased MMP expression and migration of BMSCs. Conditioned media of miR-191 overexpressing BMSCs block VEGF expression, and inhibit angiogenesis of HUVECs. Under osteogenic culture conditions, inhibition of miR-191 significantly induces bone formation. Moreover, our studies showed miR-191 might influence chondrogenesis of BMSCs by directly targeting CCAAT Enhancer Binding Protein Beta (CEBPB). Taken together, here we demonstrate the role of miR-191 in differentiation, migration and paracrine function of BMSCs.

Keywords: Differentiation; Mesenchymal stem cells; Migration; Paracrine; miR-191.

MeSH terms

  • Animals
  • CCAAT-Enhancer-Binding Protein-beta / metabolism
  • Cell Differentiation / physiology*
  • Cell Movement / physiology*
  • Cell Survival
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / metabolism
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Neovascularization, Physiologic / physiology*
  • Osteogenesis
  • Paracrine Communication / physiology*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • CCAAT-Enhancer-Binding Protein-beta
  • MIRN191 microRNA, human
  • MicroRNAs