Induction of DNA double-strand breaks in primary gingival fibroblasts by exposure to dental resin composites

被引:109
作者
Urcan, Ebru [1 ]
Scherthan, Harry [2 ]
Styllou, Marianthi [1 ]
Haertel, Uschi [1 ]
Hickel, Reinhard [3 ]
Reichl, Franz-Xaver [1 ,3 ]
机构
[1] Univ Munich, Walther Straub Inst Pharmacol & Toxicol, D-80366 Munich, Germany
[2] Univ Ulm, Bundeswehr Inst Radiobiol, D-80937 Munich, Germany
[3] Univ Munich, Dept Operat Restorat Dent Periodontol & Pedodont, D-80366 Munich, Germany
关键词
Dental resin composites; HGFs; DNA damage; DNA double-strand break; gamma-H2AX; CYTOTOXICITY; TEGDMA; MONOMERS; ELUTION; GENOTOXICITY; LYMPHOCYTES; COMPONENTS; TOXICOLOGY; APOPTOSIS;
D O I
10.1016/j.biomaterials.2009.11.065
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Dental resin composites and their reactive monomers/co-monomers have been shown to elicit cytotoxic responses in human gingival fibroblasts (HGF), and their metabolic radical intermediates have the potential to attack the DNA backbone, which may induce DNA double-strand breaks (DSBs). In this study we have tested the cytotoxicity and induction of DSBs by the most common composite resin monomers/co-monomers: BisGMA, HEMA, TEGDMA, and UDMA in gingival fibroblasts using the sensitive gamma-H2AX DNA repair focus assay. Our results show increasing monomer cytotoxicities in the order of BisGMA > UDMA > TEGDMA > HEMA, an order that was also observed for their capacity to induce DSBs. BisGMA at the EC50 concentration of 0.09 mm evoked the highest rate of gamma-H2AX foci-formation that was 11-fold higher DNA DSBs as compared to the negative controls that ranged between 0.25 and 0.5 gamma-H2AX foci/HGF cell. Our results for the first time show that exposure to dental resin monomers can induce DSBs in primary human oral cavity cells, which underscores their genotoxic capacity. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2010 / 2014
页数:5
相关论文
共 31 条
[1]   In vitro cytotoxicity and dentin permeability of HEMA [J].
Bouillaguet, S ;
Wataha, JC ;
Hanks, CT ;
Ciucchi, B ;
Holz, J .
JOURNAL OF ENDODONTICS, 1996, 22 (05) :244-248
[2]   TEGDMA-induced oxidative DNA damage and activation of ATM and MAP kinases [J].
Eckhardt, Alexander ;
Gerstmayr, Nicol ;
Hiller, Karl-Anton ;
Bolay, Carola ;
Waha, Claudia ;
Spagnuolo, Gianrico ;
Camargo, Carlos ;
Schmalz, Gottfried ;
Schweikl, Helmut .
BIOMATERIALS, 2009, 30 (11) :2006-2014
[3]   ELUTION OF LEACHABLE COMPONENTS FROM COMPOSITES [J].
FERRACANE, JL .
JOURNAL OF ORAL REHABILITATION, 1994, 21 (04) :441-452
[4]   In vitro evaluation of the marginal degradation of dental composites under simulated occlusal loading [J].
Ferracane, JL ;
Condon, JR .
DENTAL MATERIALS, 1999, 15 (04) :262-267
[5]  
FORST H, 1985, ARZNEIMITTEL-FORSCH, V35, P3
[6]   A review of saliva: Normal composition, flow, and function [J].
Humphrey, SP ;
Williamson, RT .
JOURNAL OF PROSTHETIC DENTISTRY, 2001, 85 (02) :162-169
[7]   Resin composite monomers alter MTT and LDH activity of human gingival fibroblasts in vitro [J].
Issa, Y ;
Watts, DC ;
Brunton, PA ;
Waters, CM ;
Duxbury, AJ .
DENTAL MATERIALS, 2004, 20 (01) :12-20
[8]   TEGDMA causes apoptosis in primary human gingival fibroblasts [J].
Janke, V ;
von Neuhoff, N ;
Schlegelberger, B ;
Leyhausen, G ;
Geurtsen, W .
JOURNAL OF DENTAL RESEARCH, 2003, 82 (10) :814-818
[9]   Cytotoxic and genotoxic effects of resin monomers in human salivary gland tissue and lymphocytes as assessed by the single cell microgel electrophoresis (Comet) assay [J].
Kleinsasser, NH ;
Schmid, K ;
Sassen, AW ;
Harréus, UA ;
Staudenmaier, R ;
Folwaczny, M ;
Glas, J ;
Reichl, FX .
BIOMATERIALS, 2006, 27 (09) :1762-1770
[10]   Genotoxicity and cytotoxicity of dental materials in human lymphocytes as assessed by the single cell microgel electrophoresis (comet) assay [J].
Kleinsasser, NH ;
Wallner, BC ;
Harréus, UA ;
Kleinjung, T ;
Folwaczny, M ;
Hickel, R ;
Kehe, K ;
Reichl, FX .
JOURNAL OF DENTISTRY, 2004, 32 (03) :229-234