Stimulation of glutathione depletion, ROS production and cell cycle arrest of dental pulp cells and gingival epithelial cells by HEMA

被引:196
作者
Chang, HH
Guo, MK
Kasten, FH
Chang, MC
Huang, GF
Wang, YL
Wang, RS
Jeng, JH
机构
[1] Natl Taiwan Univ Hosp, Dept Dent, Grad Inst Clin Dent Sci, Lab Dent Pharmacol, Taipei 100, Taiwan
[2] Natl Taiwan Univ, Coll Med, Taipei 10018, Taiwan
[3] E Tennessee State Univ, Johnson City, TN 37614 USA
[4] Chang Gung Inst Technol, Biomed Sci Team, Taoyuan, Taiwan
[5] Natl Taiwan Univ, Grad Inst Clin Dent Sci, Lab Dent Pharmacol & Toxicol, Taipei 10764, Taiwan
关键词
apoptosis; cell cycle; glutathione; HEMA; pulp cells; gingival cells; reactive oxygen species; toxicity;
D O I
10.1016/j.biomaterials.2004.03.021
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
2-Hydroxy-ethyl methacrylate (HEMA) is the major component released from resin-modified glass ionomer cements and dental adhesives. Human tissues mainly affected by HEMA are oral epithelium and dental pulp. We treated human gingival epithelial S-G cells and pulp fibroblasts (HPF) with various concentrations of HEMA, to evaluate its effects on cell growth, cell cycle progression, intracellular glutathione (GSH) level and reactive oxygen species (ROS) production. HEMA-induced growth inhibition in HPF and S-G cells in a dose-dependent manner, which may be partially explained by induction of cell cycle perturbation. G(2)/M phase arrest was noted after exposure of HPF to 5 and 10 mM of HEMA, concomitant with glutathione depletion and ROS production. S-phase arrest occurred in S-G cells when treated with 2.5 and 5 mm, while at 10 mm a sub-G(0)/G(1) peak was noted, indicating the potential induction of apoptosis. GSH depletion was marked in S-G cells only at concentrations of 5 and 10 mM, but excessive ROS production was noted at concentration of 1 mM and rose with dose increase between 1 and 5 mm, then lessened at 10 mm. This suggested that the increase of ROS in S-G cells was not mainly caused by GSH depletion. These results helped to define the mechanism of the cytotoxicity caused by HEMA. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:745 / 753
页数:9
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