microRNA-21a-5p/PDCD4 axis regulates mesenchymal stem cell-induced neuroprotection in acute glaucoma

J Mol Cell Biol. 2017 Aug 1;9(4):289-301. doi: 10.1093/jmcb/mjx022.

Abstract

Mesenchymal stem cells (MSCs) have been demonstrated to have promising therapeutic benefits for a variety of neurological diseases; however, the underlying mechanisms are poorly understood. Here, we showed that intravitreal infusion of MSCs promoted retinal ganglion cell (RGC) survival in a mouse model of acute glaucoma, with significant inhibition of microglial activation, production of TNF-α, IL-1β, and reactive oxygen species, as well as caspase-8 and caspase-3 activation. In vitro, MSCs inhibited both caspase-8-mediated RGC apoptosis and microglial activation, partly via the action of stanniocalcin 1 (STC1). Furthermore, we found that microRNA-21a-5p (miR-21) and its target, PDCD4, were essential for STC1 production and the neuroprotective property of MSCs in vitro and in vivo. Importantly, miR-21 overexpression or PDCD4 knockdown augmented MSC-mediated neuroprotective effects on acute glaucoma. These data highlight a previously unrecognized neuroprotective mechanism by which the miR-21/PDCD4 axis induces MSCs to secrete STC1 and other factors that exert neuroprotective effects. Therefore, modulating the miR-21/PDCD4 axis might be a promising strategy for clinical treatment of acute glaucoma and other neurological diseases.

Keywords: glaucoma; mesenchymal stem cells; microRNA; neurological diseases; neuroprotection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Animals
  • Apoptosis Regulatory Proteins / genetics
  • Apoptosis Regulatory Proteins / metabolism*
  • Cell Survival
  • Cells, Cultured
  • Disease Models, Animal
  • Down-Regulation
  • Glaucoma / genetics
  • Glaucoma / metabolism
  • Glaucoma / pathology
  • Glaucoma / therapy*
  • Intravitreal Injections
  • Male
  • Mesenchymal Stem Cell Transplantation* / methods
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / metabolism
  • Mice
  • Mice, Inbred C57BL
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Neuroprotection
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism*
  • Retinal Ganglion Cells / cytology*
  • Retinal Ganglion Cells / metabolism
  • Retinal Ganglion Cells / pathology
  • Signal Transduction*
  • Up-Regulation

Substances

  • Apoptosis Regulatory Proteins
  • MIRN21 microRNA, mouse
  • MicroRNAs
  • Pdcd4 protein, mouse
  • RNA-Binding Proteins