Combination of ions promotes cell migration via extracellular signal-regulated kinase 1/2 signaling pathway in human gingival fibroblasts

Kimiko Yamaguchi-Ueda, Yuki Akazawa, Keita Kawarabayashi, Asuna Sugimoto, Hiroshi Nakagawa, Aya Miyazaki, Rika Kurogoushi, Kokoro Iwata, Takamasa Kitamura, Aya Yamada, Tomokazu Hasegawa, Satoshi Fukumoto, Tsutomu Iwamoto

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Wound healing is a dynamic process that involves highly coordinated cellular events, including proliferation and migration. Oral gingival fibroblasts serve a central role in maintaining oral mucosa homeostasis, and their functions include the coordination of physiological tissue repair. recently, surface pre-reacted glass-ionomer (S-PRG) fillers have been widely applied in the field of dental materials for the prevention of dental caries, due to an excellent ability to release fluoride (F). In addition to F, S-PRG fillers are known to release several types of ions, including aluminum (Al), boron (B), sodium (Na), silicon (Si) and strontium (Sr). However, the influence of these ions on gingival fibroblasts remains unknown. The aim of the present study was to examine the effect of various concentrations of an S-PRG filler eluate on the growth and migration of gingival fibroblasts. The human gingival fibroblast cell line HGF-1 was treated with various dilutions of an eluent solution of S-PrG, which contained 32.0 ppm al, 1,488.6 ppm B, 505.0 ppm Na, 12.9 ppm Si, 156.5 ppm Sr and 136.5 ppm F. Treatment with eluate at a dilution of 1:10,000 was observed to significantly promote the migration of HGF-1 cells. in addition, the current study evaluated the mechanism underlying the mediated cell migration by the S-PRG solution and revealed that it activated the phosphorylation of extracellular signal-regulated kinase 1/2 (erK1/2), but not of p38. Furthermore, treatment with a MEK inhibitor blocked the cell migration induced by the solution. Taken together, these results suggest that S-PRG fillers can stimulate HGF-1 cell migration via the erK1/2 signaling pathway, indicating that a dental material containing this type of filler is useful for oral mucosa homeostasis and wound healing.

Original languageEnglish
Pages (from-to)5039-5045
Number of pages7
JournalMolecular medicine reports
Volume19
Issue number6
DOIs
Publication statusPublished - 2019 Jan 1

Keywords

  • Cell migration
  • Extracellular signal-regulated kinase signaling
  • Gingival fibroblasts
  • Multiple-ion solution
  • Surface pre-reacted glass-ionomer filler

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Medicine
  • Molecular Biology
  • Genetics
  • Oncology
  • Cancer Research

Fingerprint Dive into the research topics of 'Combination of ions promotes cell migration via extracellular signal-regulated kinase 1/2 signaling pathway in human gingival fibroblasts'. Together they form a unique fingerprint.

  • Cite this

    Yamaguchi-Ueda, K., Akazawa, Y., Kawarabayashi, K., Sugimoto, A., Nakagawa, H., Miyazaki, A., Kurogoushi, R., Iwata, K., Kitamura, T., Yamada, A., Hasegawa, T., Fukumoto, S., & Iwamoto, T. (2019). Combination of ions promotes cell migration via extracellular signal-regulated kinase 1/2 signaling pathway in human gingival fibroblasts. Molecular medicine reports, 19(6), 5039-5045. https://doi.org/10.3892/mmr.2019.10141