Cytokines induce MMP-3-regulated proliferation of embryonic stem cell-derived odontoblast-like cells

Oral Dis. 2014 Jul;20(5):505-13. doi: 10.1111/odi.12165. Epub 2013 Aug 1.

Abstract

Objectives: Matrix metalloproteinase (MMP)-3 expression increases after pulpectomy and accelerates angiogenesis in rat dental pulp by an uncharacterised mechanism. Odontoblasts, a major component of dental pulp, could represent a therapeutic target. We investigated whether MMP-3 activity is induced by cytokines and/or is associated with cell proliferation and apoptosis in embryonic stem cell-derived odontoblast-like cells.

Materials and methods: We used reverse transcriptase polymerase chain reaction, western blotting, an MMP-3 activity assay, a BrdU-cell proliferation enzyme-linked immunosorbent assay and DNA fragmentation analysis to evaluate siRNA-mediated downregulation of MMP-3 expression and activity, and any changes in the proliferative and apoptotic responses associated with this reduced expression.

Results: Pro-inflammatory cytokines (interleukin-1β, tumour necrosis factor-α and interferon-γ, at relatively low concentrations) induced MMP-3 mRNA and protein expression, and increased MMP-3 activity and cell proliferation, but not apoptosis. MMP-3 silencing produced a potent and significant suppression of cytokine-induced MMP-3 expression and activity, decreased cell proliferation and increased apoptosis. These effects were rescued by application of exogenous MMP-3.

Conclusions: Our results suggest that pro-inflammatory cytokines induce MMP-3-regulated cell proliferation and anti-apoptosis effects in odontoblast-like cells derived from embryonic stem cells, in addition to their well-documented destructive role in inflammation.

Keywords: cytokines; embryonic stem cells; inflammation; matrix metalloproteinase; odontoblast.

Publication types

  • Research Support, Non-U.S. Gov't
  • Retracted Publication

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Blotting, Western
  • Cell Division / physiology
  • Cell Line
  • Cell Proliferation*
  • Cytokines / physiology*
  • Embryonic Stem Cells / cytology*
  • Matrix Metalloproteinase 3 / physiology*
  • Mice
  • Odontoblasts / cytology*
  • Odontoblasts / drug effects
  • Proteins

Substances

  • Cytokines
  • Proteins
  • reducing agent and tunicamycin-responsive protein, human
  • Matrix Metalloproteinase 3
  • Mmp3 protein, mouse