Cyclic tensile force-upregulated IL6 increases MMP3 expression by human periodontal ligament cells

Arch Oral Biol. 2019 Nov:107:104495. doi: 10.1016/j.archoralbio.2019.104495. Epub 2019 Jul 26.

Abstract

Objective: Cyclic tensile force (CTF) modulates physiological responses of periodontal ligament (PDL) cells. PDL cells are mechanosensitive and are able to maintain tissue homeostasis; a process mediated by the expression of particular cytokines including interleukin 6 (IL6). It is unknown whether CTF-induced IL6 regulates the expression of MMPs, enzymes needed for tissue remodeling.

Design: Human PDL cells were subjected to 10% elongation strain of CTF at a frequency of 60 rpm continuously for 6 h. RNA and proteins were extracted and analyzed for IL6 and MMP expression by quantitative real-time PCR and ELISA, respectively. Using a neutralizing anti-IL6 antibody and addition of recombinant human IL6 at concentrations of 0.1, 1, 10 ng.mL-1 were performed to clarify whether CTF-upregulated IL6 increased MMP expression. Inhibitors of intracellular signaling molecules were employed to reveal possible pathway(s) of IL6-induced MMP expression.

Results: CTF-induced IL6 expression coincided with an increased MMP3 expression. A neutralizing anti-IL6 antibody attenuated the CTF-increased MMP3 expression, whereas stimulating the cells with recombinant human IL6 increased MMP3 expression. Both PI3K and MAPK pathways were essential in the IL6 induced expression of MMP3.

Conclusion: Our findings suggest a role of CTF in the modulation of expression of IL6 and MMP3 and thus in the regulation of homeostasis and remodeling of the periodontal ligament.

Keywords: Cyclic tensile force; Human periodontal ligament cells; IL6; MMP3.

MeSH terms

  • Cells, Cultured
  • Humans
  • Interleukin-6 / metabolism*
  • Matrix Metalloproteinase 3 / metabolism*
  • Periodontal Ligament / cytology*
  • Signal Transduction
  • Stress, Mechanical*
  • Up-Regulation

Substances

  • IL6 protein, human
  • Interleukin-6
  • MMP3 protein, human
  • Matrix Metalloproteinase 3