Influence of clodronate and compressive force on IL-1ß-stimulated human periodontal ligament fibroblasts

Clin Oral Investig. 2020 Jan;24(1):343-350. doi: 10.1007/s00784-019-02930-z. Epub 2019 May 17.

Abstract

Objectives: The aim of this study was to investigate in vitro the effect of clodronate on interleukin-1ß (IL-1ß)-stimulated human periodontal ligament fibroblasts (HPdLFs) with the focus on inflammatory factors of orthodontic tooth movement with and without compressive force.

Materials and methods: HPdLFs were incubated with 5 μM clodronate and 10 ng/mL IL-1ß. After 48 h, cells were exposed to 3 h of compressive force using a centrifuge. The gene expression of cyclooxygenase-2 (COX-2), interleukin-6 (IL-6), matrix metalloproteinase 8 (MMP-8), and the tissue inhibitor of MMP (TIMP-1) was analyzed using RT-PCR. Prostaglandin E2 (PGE-2), IL-6, and TIMP-1 protein syntheses were quantified via ELISA.

Results: Compressive force and IL-1ß induced an overexpression of COX-2 gene expression (61.8-fold; p < 0.05 compared with control), diminished by clodronate (41.1-fold; p < 0.05 compared with control). Clodronate slowed down the compression and IL-1ß induced IL-6 gene expression (161-fold vs. 85.6-fold; p < 0.05 compared with control). TNF-α was only slightly affected without statistical significance. Clodronate reduced IL-1ß-stimulated MMP-8 expression with and without compressive force. TIMP-1 on gene and protein level was downregulated in all groups. Analyzing the MMP-8/TIMP-1 ratio, the highest ratio was detected in IL-1ß-stimulated HPdLFs with compressive force (21.2-fold; p < 0.05 compared with control). Clodronate diminished IL-1ß-induced upregulation of MMP-8/TIMP-1 ratio with (11.5-fold; p < 0.05 compared with control) and without (12.5-fold; p < 0.05 compared with control) compressive force.

Conclusion: Our study demonstrates a slightly anti-inflammatory effect by clodronate under compressive force in vitro. Additionally, the periodontal remodeling presented by the MMP-8/TIMP-1 ratio seems to be diminished by clodronate.

Clinical relevance: Reduction of pro-inflammatory factors and reduction of periodontal remodeling might explain reduced orthodontic tooth movement under clodronate intake.

Keywords: Clodronate; Compressive force; Non-nitrogen-containing bisphosphonate; Periodontal ligament; Tooth movement.

MeSH terms

  • Biomechanical Phenomena
  • Cells, Cultured
  • Clodronic Acid* / pharmacology
  • Dinoprostone
  • Fibroblasts
  • Humans
  • Interleukin-1beta* / physiology
  • Matrix Metalloproteinase 8 / metabolism
  • Periodontal Ligament* / drug effects
  • Periodontal Ligament* / metabolism
  • Tissue Inhibitor of Metalloproteinase-1 / metabolism
  • Tooth Movement Techniques

Substances

  • Interleukin-1beta
  • TIMP1 protein, human
  • Tissue Inhibitor of Metalloproteinase-1
  • Clodronic Acid
  • MMP8 protein, human
  • Matrix Metalloproteinase 8
  • Dinoprostone

Grants and funding