MiRNA-486 regulates angiogenic activity and survival of mesenchymal stem cells under hypoxia through modulating Akt signal

Biochem Biophys Res Commun. 2016 Feb 12;470(3):670-677. doi: 10.1016/j.bbrc.2016.01.084. Epub 2016 Jan 20.

Abstract

MicroRNA-486 (miR-486) was first identified from human fetal liver cDNA library and validated as a regulator of hematopoiesis. Its roles in regulating the biological function of bone marrow-derived mesnechymal stem cells (BM-MSCs) under hypoxia have not been explored yet. In this study, we demonstrated that exposure to hypoxia upregulates miR-486 expression in BM-MSCs. Lentivirus-mediated overexpression of miR-486 resulted in increase of hepatocyte growth factor (HGF) and vascular endothelial growth factor(VEGF) in both mRNA and protein levels. MiR-486 expression also promotes proliferation and reduces apoptosis of BM-MSCs. Whereas MiR-486 knockdown downregulated the secretion of HGF and VEGF and induced apoptosis of BM-MSCs. Furthermore, PTEN-PI3K/AKT signaling was validated to be involved in changes of BM-MSC biological functions regulated by miR-486. These results suggested that MiR-486 mediated the hypoxia-induced angiogenic activity and promoted the proliferation and survival of BM-MSCs through regulating PTEN-PI3K/AKT signaling. These findings might provide a novel understanding of effective therapeutic strategy for hypoxic-ischemic diseases.

Keywords: Bone marrow mesenchymal stem cells; Hypoxia; PTEN-PI3K/AKT signaling; miR-486.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiogenic Proteins / metabolism
  • Cell Differentiation / physiology
  • Cell Hypoxia / physiology
  • Cell Movement / physiology
  • Cell Survival / physiology
  • Cells, Cultured
  • Gene Expression Regulation / physiology
  • Humans
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / physiology*
  • MicroRNAs / metabolism*
  • Neovascularization, Physiologic / physiology*
  • Oncogene Protein v-akt / metabolism*
  • Oxygen / metabolism*
  • Signal Transduction / physiology

Substances

  • Angiogenic Proteins
  • MIRN486 microRNA, human
  • MicroRNAs
  • Oncogene Protein v-akt
  • Oxygen