Compressive force stimulates the gene expression of IL-17s and their receptors in MC3T3-E1 cells

Connect Tissue Res. 2010 Oct;51(5):359-69. doi: 10.3109/03008200903456942.

Abstract

During orthodontic tooth movement, cytokines released from periodontal ligament fibroblasts and alveolar bone osteoblasts can alter the process of bone remodeling. Recently, interleukin-17 (IL-17) was found to stimulate osteoclastic resorption through osteoblasts by inducing receptor activator of nuclear factor κB ligand (RANKL) expression. However, the relationship between mechanical stress and IL-17 production by osteoblasts is not clear. Therefore, we examined the effect of compressive force on the expressions of IL-17A, IL-17B, IL-17C, IL-17D, IL-17E, IL-17F, and their receptors (IL-17RA, IL-17RB, IL-17RC, IL-17RD, and IL-17RE) using MC3T3-E1 cells as osteoblast-like cells. We also examined the effect of IL-17A on the expression of IL-17Rs, RANKL, macrophage colony-stimulating factor (M-CSF), and osteoprotegerin (OPG). The cells were cultured with or without continuous compressive force (1.0 and 2.0 g/cm(2)) for up to 24 hr. The cells were also cultured with or without IL-17A (0.1, 1.0, or 10 ng/ml) for up to 72 hr. The mRNA expressions of IL-17s and their receptors were estimated by real-time polymerase chain reaction. The expression levels of IL-17s and their receptors increased depending on the compressive force. The addition of IL-17A increased the expression of IL-17RA, IL-17RB, IL-17RC, IL-17RE, RANKL, and M-CSF, whereas it decreased OPG expression. These results indicate that compressive force induces the expression of IL-17s and their receptors in osteoblast-like cells and that IL-17s and their receptors produced in response to compressive force may affect osteoclastogenesis through the expression of RANKL, M-CSF, and OPG.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Animals
  • Compressive Strength / physiology*
  • Gene Expression Regulation / physiology*
  • Interleukin-17 / biosynthesis*
  • Interleukin-17 / genetics
  • Macrophage Colony-Stimulating Factor / biosynthesis
  • Macrophage Colony-Stimulating Factor / genetics
  • Mice
  • Osteoblasts / metabolism*
  • Osteoprotegerin / biosynthesis
  • Osteoprotegerin / genetics
  • RANK Ligand / biosynthesis
  • RANK Ligand / genetics
  • Receptors, Interleukin-17 / biosynthesis*
  • Receptors, Interleukin-17 / genetics
  • Stress, Mechanical*

Substances

  • Interleukin-17
  • Osteoprotegerin
  • RANK Ligand
  • Receptors, Interleukin-17
  • Macrophage Colony-Stimulating Factor