Response of oral mucosal cells to glass ionomer cements

J. Lewis, L. Nix, G. Schuster, Carol A Lefebvre, K. Knoernschild, Gretchen B Caughman

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

Although glass ionomer cements are generally considered to be tissue-compatible, it has been suggested that unreacted components or setting reaction by-products can affect cell metabolism. The current study examined the effects of constituents leached out of three glass ionomer cements on growth and metabolism of oral epithelial cells. Aseptically prepared discs of Ketac-Cem Radiopaque (KCR), Ketac-Cem Maxicap (KCM) and Fuji I were incubated in Dulbecco's medium for 10 d, with daily medium changes. Cultures of hamster cheek pouch (HCP) cells, a line of hamster buccal pouch epithelial cells, were incubated in control or eluate-containing media for 24 h. Viable cell numbers were determined by the colorimetric MTS assay, and DNA and RNA syntheses were assessed using [3H]thymidine and [3H]uridine incorporation, respectively. Responses to materials were determined by comparison of cell numbers and radioisotope incorporation (counts per minute (cpm) per 1000 cells). Results were analysed by ANOVA and Duncan's multiple range test, then converted to percent control for comparison. The eluates of all three materials from the first 24 h of soaking inhibited HCP cell growth. The number of cells in cultures exposed to Fuji were 88% of control cultures, while those exposed to KCR and KCM were 58% and 59% of control, respectively. The difference between Fuji-exposed and control cultures was significant (P < 0.05). The two Ketac cements were different from Fuji-exposed and control cultures (P < 0.05) but not from each other. All of the materials caused significant increases in labelling of DNA compared to control cultures (P < 0.05) when calculated on a per cell basis, but the materials did not differ from each other. Both Ketac cements also significantly stimulated labelling of RNA per cell compared to control cultures (P < 0.05). All effects of the material decreased over time. Results suggest that leachable components of the materials may affect the rate of progression of HCP cells through the cell cycle, rather than overt toxicity that results in cell death.

Original languageEnglish (US)
Pages (from-to)1115-1120
Number of pages6
JournalBiomaterials
Volume17
Issue number11
DOIs
StatePublished - Jan 1 1996

Fingerprint

Glass Ionomer Cements
Ionomers
Cements
Cheek
Glass
Cricetinae
Cell Count
Epithelial Cells
RNA
Metabolism
Labeling
DNA
Uridine
Growth
Radioisotopes
Thymidine
Analysis of Variance
Cell Cycle
Cell growth
Cell Death

Keywords

  • DNA synthesis
  • Fluoride
  • Glass ionomer cements
  • MTS assay
  • Oral epithelial cells
  • RNA synthesis

ASJC Scopus subject areas

  • Bioengineering
  • Ceramics and Composites
  • Biophysics
  • Biomaterials
  • Mechanics of Materials

Cite this

Response of oral mucosal cells to glass ionomer cements. / Lewis, J.; Nix, L.; Schuster, G.; Lefebvre, Carol A; Knoernschild, K.; Caughman, Gretchen B.

In: Biomaterials, Vol. 17, No. 11, 01.01.1996, p. 1115-1120.

Research output: Contribution to journalArticle

Lewis, J. ; Nix, L. ; Schuster, G. ; Lefebvre, Carol A ; Knoernschild, K. ; Caughman, Gretchen B. / Response of oral mucosal cells to glass ionomer cements. In: Biomaterials. 1996 ; Vol. 17, No. 11. pp. 1115-1120.
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