Suppression of miR-181a attenuates H2O2-induced death of mesenchymal stem cells by maintaining hexokinase II expression

Biol Res. 2015 Aug 18;48(1):45. doi: 10.1186/s40659-015-0036-5.

Abstract

Background: Low survival rate of transplanted cells compromises the efficacy of cell therapy. Hexokinase II (HKII) is known to have anti-apoptotic activity through its interaction with mitochondria. The objective was to identify miRNAs targeting HKII and investigate whether miRNA-mediated modulation of HKII could improve the survival of mesenchymal stem cells (MSCs) exposed to H2O2. The expression of HKII in MSCs exposed to H2O2 was evaluated, and HKII-targeting miRNA was screened based on miRNA-target prediction databases. The effect of H2O2 on the expression of the selected HKII-targeting miRNA was examined and the effect of modulation of the selected HKII-targeting miRNA using anti-miRNA on H2O2-induced apoptosis of MSC was evaluated.

Results: H2O2 (600 μM) induced cell death of MSCs and decreased mitochondrial HKII expression. We have identified miR-181a as a HKII-targeting miRNA and H2O2 increased the expression of miR-181a in MSCs. Delivery of anti-miR-181a, which neutralizes endogenous miR-181a, significantly attenuated H2O2-induced decrease of HKII expression and disruption of mitochondrial membrane potential, improving the survival of MSCs exposed to H2O2.

Conclusions: These findings suggest that H2O2-induced up-regulation of miR-181a contributes to the cell death of MSCs by down-regulating HKII. Neutralizing miR-181a can be an effective way to prime MSCs for transplantation into ischemic tissues.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis*
  • Cell Differentiation
  • Cell Movement
  • Cell Survival
  • Glioma / metabolism
  • Glioma / pathology*
  • Hexokinase / metabolism*
  • Humans
  • Hydrogen Peroxide / administration & dosage
  • Hydrogen Peroxide / toxicity*
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / enzymology
  • Mesenchymal Stem Cells / pathology*
  • MicroRNAs / antagonists & inhibitors
  • MicroRNAs / metabolism*
  • Mitochondria / enzymology
  • Neoplasm Invasiveness
  • Reactive Oxygen Species
  • Real-Time Polymerase Chain Reaction
  • Semaphorins / genetics
  • Semaphorins / metabolism

Substances

  • MIrn181 microRNA, human
  • Membrane Glycoproteins
  • MicroRNAs
  • Reactive Oxygen Species
  • SEMA3B protein, human
  • Semaphorins
  • Hydrogen Peroxide
  • Hexokinase