miR-34a regulates mesangial cell proliferation via the PDGFR-β/Ras-MAPK signaling pathway

Cell Mol Life Sci. 2014 Oct;71(20):4027-42. doi: 10.1007/s00018-014-1599-y. Epub 2014 Mar 18.

Abstract

The main pathological characteristic of glomerulonephritis is diffuse mesangial cell proliferation. MiR-34a is associated with the proliferation of various organs and cancer cells. However, the role of miR-34a in renal proliferation diseases is not clear. Therefore, this study aimed to elucidate the mechanism of miR-34a in the regulation of renal mesangial cell proliferation. The miR-34a expression level at different time points in an anti-Thy1 mesangial proliferative nephritis rat model was determined by qRT-PCR. The cell proliferation rate and cell cycle changes were measured in the in vitro cultured rat mesangial cells (RMCs). Our results suggested that miR-34a expression was negatively correlated with the degree of cell proliferation in the anti-Thy1 nephritis model. MiR-34a could extend the G0/G1 phase and block cell proliferation in RMCs. Dual-luciferase assay results showed that there were binding sites of miR-34a at 3'-UTR of platelet-derived growth factor receptor-β (PDGFR-β). MiR-34a can inhibit PDGFR-β protein expression at a post-transcriptional level, suppress Ras/MAPK signaling pathways, and down-regulate expression of cell cycle proteins at the G0/G1 phase, such as cyclin D1, CDK4/CDK6. In addition, miR-34a may also inhibit RMC proliferation by directly targeting cyclin E and CDK2. MiR-34a inhibits exogenous stimuli-induced proliferation of mesangial cells. Expression levels of phospho-PDGFR-β and phospho-MEK1 (an important downstream molecule in PDGFR-β-induced signaling pathway) were significantly increased in the anti-Thy-1 nephritis rat model. These results suggest that miR-34a may regulate RMC proliferation by directly inhibiting expressions of PDGFR-β, MEK1, and cell cycle proteins, cyclin E and CDK2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions
  • Animals
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism
  • Cell Line
  • Cell Proliferation
  • G1 Phase
  • Glomerulonephritis / metabolism
  • Glomerulonephritis / pathology
  • Isoantibodies / immunology
  • Mesangial Cells / cytology
  • Mesangial Cells / metabolism*
  • MicroRNAs / metabolism*
  • Mitogen-Activated Protein Kinase Kinases / metabolism*
  • RNA Interference
  • RNA, Small Interfering / metabolism
  • Rats
  • Rats, Wistar
  • Receptor, Platelet-Derived Growth Factor beta / antagonists & inhibitors
  • Receptor, Platelet-Derived Growth Factor beta / genetics
  • Receptor, Platelet-Derived Growth Factor beta / metabolism
  • Signal Transduction
  • ras Proteins / metabolism*

Substances

  • 3' Untranslated Regions
  • Cell Cycle Proteins
  • Isoantibodies
  • MIRN34 microRNA, rat
  • MicroRNAs
  • RNA, Small Interfering
  • anti-Thy antibody
  • Receptor, Platelet-Derived Growth Factor beta
  • Mitogen-Activated Protein Kinase Kinases
  • ras Proteins