Effects of BisGMA on glutathione metabolism and apoptosis in human gingival fibroblasts in vitro

被引:82
作者
Engelmann, J
Janke, V
Volk, J
Leyhausen, G
Von Neuhoff, N
Schlegelberger, B
Geurtsen, W
机构
[1] Univ Washington, Dept Restorat Dent, Seattle, WA 98195 USA
[2] Hannover Med Sch, Inst Cell & Mol Pathol, Hannover, Germany
[3] Univ Washington, Dept Conservat Dent & Periodontol, Seattle, WA 98195 USA
关键词
gingival fibroblasts; BisGMA; apoptosis; glutathione;
D O I
10.1016/j.biomaterials.2003.11.048
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Aim of this study was to investigate the effects of the resin monomer BisGMA on the glutathione concentration (monobromobimane assay) and apoptosis (Annexin V/PI-assay) of cultured primary human gingival fibroblasts. Cells were treated for up to 24 h with 0.001-0.25 mm BisGMA to determine growth curves using the DNA stain H33342. Subsequent Annexin V/PI-assays revealed that fibroblasts exposed to concentrations of 0.005-0.01 mm (non-cytotoxic) and 0.05 mm (ED10-concentration) showed no increase of the share of apoptotic cells compared to non-treated controls (5-8%), while 0.1 mm BisGMA (similar to ED50-concentration) caused a significant increase of the percentage of apoptotic cells (50%). Simultaneously to the induction of apoptosis, 0.1 and 0.25 mm of BisGMA caused a significant depletion of the intracellular GSH content after 18 h of incubation. Our results indicate that BisGMA at concentrations > 0.1 mm causes an extreme depletion of the intracellular GSH pool as well as apoptosis. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4573 / 4580
页数:8
相关论文
共 37 条
[1]   Time-related bisphenol-A content and estrogenic activity in saliva samples collected in relation to placement of fissure sealants. [J].
Arenholt-Bindslev D. ;
Breinholt V. ;
Preiss A. ;
Schmalz G. .
Clinical Oral Investigations, 1999, 3 (3) :120-125
[2]   Bisphenol A and its biomaterial monomer derivatives alteration of in vitro cytochrome P450 metabolism in rat, minipig, and human [J].
Cannon, JM ;
Kostoryz, E ;
Russo, KA ;
Smith, RE ;
Yourtee, DM .
BIOMACROMOLECULES, 2000, 1 (04) :656-664
[3]   Patterns of cell death induced by eluates from denture base acrylic resins in U-937 human monoblastoid cells [J].
Cimpan, MR ;
Cressey, LI ;
Skaug, N ;
Halstensen, A ;
Lie, SA ;
Gjertsen, BT ;
Matre, R .
EUROPEAN JOURNAL OF ORAL SCIENCES, 2000, 108 (01) :59-69
[4]  
Costa CAS, 2000, AM J DENT, V13, P81
[5]   EVIDENCE THAT BASEMENT-MEMBRANE PREVENTS APOPTOSIS OF SERTOLI CELLS IN-VITRO IN THE ABSENCE OF KNOWN REGULATORS OF SERTOLI-CELL FUNCTION [J].
DIRAMI, G ;
RAVINDRANATH, N ;
KLEINMAN, HK ;
DYM, M .
ENDOCRINOLOGY, 1995, 136 (10) :4439-4447
[6]   Effect of TEGDMA on the intracellular glutathione concentration of human gingival fibroblasts [J].
Engelmann, J ;
Leyhausen, G ;
Leibfritz, D ;
Geurtsen, W .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 2002, 63 (06) :746-751
[7]   CURRENT TRENDS IN DENTAL COMPOSITES [J].
FERRACANE, JL .
CRITICAL REVIEWS IN ORAL BIOLOGY AND MEDICINE, 1995, 6 (04) :302-318
[8]  
Geurtsen W, 1998, J BIOMED MATER RES, V41, P474, DOI 10.1002/(SICI)1097-4636(19980905)41:3<474::AID-JBM18>3.0.CO
[9]  
2-I
[10]   Biocompatibility of resin-modified filling materials [J].
Geurtsen, W .
CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE, 2000, 11 (03) :333-355