The effects of cytotoxicity and genotoxicity induced by 2,2-bis[4-(acryloxypropoxy)phenyl]propane via caspases in human gingival fibroblasts

被引:7
作者
Yang, Ming-Ling [1 ]
机构
[1] Chung Shan Med Univ, Sch Med, Dept Anat, Taichung 402, Taiwan
关键词
BAPP; human gingival fibroblast; cytotoxicity; genotoxicity; apoptosis; caspases; DNA-DAMAGE; IN-VITRO; HUMAN-LYMPHOCYTES; RESIN MONOMERS; CELL-DEATH; RESTORATIVE MATERIALS; BISPHENOL-A; COMET ASSAY; APOPTOSIS; INDUCTION;
D O I
10.1177/0748233712462472
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The toxicity of dental materials has raised public concern over the past years. One of the most commonly used methacrylic monomers for building the three-dimensional structure of the dental resin composites is 2,2-bis[4-(acryloxypropoxy)phenyl]propane (BAPP). The purpose of this study is to evaluate the potential toxicological implication of BAPP on human gingival fibroblasts (HGFs). Flow cytometric, fluorometric, and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) colorimetric assays were used to detect the mode of cell death, caspase activities, and cell viability, respectively. In addition, alkaline single-cell gel electrophoresis (COMET) and cytokinesis block micronucleus (MN) assays were applied to evaluate the genotoxicity. According to the results BAPP demonstrated a cytotoxic effect on HGFs in a dose- and time-dependent manner. With increasing concentrations of BAPP, the mode of cell death shifted from apoptosis to necrosis, and the activities of caspases 3, 8, and 9 were also significantly induced. Moreover, a dose-related increase in the number of micronucleus and DNA strand breaks hinted at the expression of genotoxicity by BAPP. In conclusion, the results gathered from this study had demonstrated that BAPP-induced cytotoxicity and genotoxicity on HGFs were mediated by DNA damage and the activation of caspases 3, 8, and 9.
引用
收藏
页码:755 / 764
页数:10
相关论文
共 39 条
  • [31] The induction of micronuclei in vitro by unpolymerized resin monomers
    Schweikl, H
    Schmalz, G
    Spruss, T
    [J]. JOURNAL OF DENTAL RESEARCH, 2001, 80 (07) : 1615 - 1620
  • [32] In vitro embryotoxicity assessment with dental restorative materials
    Schwengberg, S
    Bohlen, H
    Kleinsasser, N
    Kehe, K
    Seiss, M
    Walther, UI
    Hickel, R
    Reichl, FX
    [J]. JOURNAL OF DENTISTRY, 2005, 33 (01) : 49 - 55
  • [33] A SIMPLE TECHNIQUE FOR QUANTITATION OF LOW-LEVELS OF DNA DAMAGE IN INDIVIDUAL CELLS
    SINGH, NP
    MCCOY, MT
    TICE, RR
    SCHNEIDER, EL
    [J]. EXPERIMENTAL CELL RESEARCH, 1988, 175 (01) : 184 - 191
  • [34] Söderholm KJ, 1999, J AM DENT ASSOC, V130, P201
  • [35] Mitochondrial dynamics and apoptosis
    Suen, Der-Fen
    Norris, Kristi L.
    Youle, Richard J.
    [J]. GENES & DEVELOPMENT, 2008, 22 (12) : 1577 - 1590
  • [36] Induction of DNA double-strand breaks in primary gingival fibroblasts by exposure to dental resin composites
    Urcan, Ebru
    Scherthan, Harry
    Styllou, Marianthi
    Haertel, Uschi
    Hickel, Reinhard
    Reichl, Franz-Xaver
    [J]. BIOMATERIALS, 2010, 31 (08) : 2010 - 2014
  • [37] MECHANISMS OF PHOSPHATIDYLSERINE EXPOSURE, A PHAGOCYTE RECOGNITION SIGNAL, ON APOPTOTIC T-LYMPHOCYTES
    VERHOVEN, B
    SCHLEGEL, RA
    WILLIAMSON, P
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (05) : 1597 - 1601
  • [38] A NOVEL ASSAY FOR APOPTOSIS - FLOW CYTOMETRIC DETECTION OF PHOSPHATIDYLSERINE EXPRESSION ON EARLY APOPTOTIC CELLS USING FLUORESCEIN-LABELED ANNEXIN-V
    VERMES, I
    HAANEN, C
    STEFFENSNAKKEN, H
    REUTELINGSPERGER, C
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 1995, 184 (01) : 39 - 51
  • [39] Wyllie A H, 1980, Int Rev Cytol, V68, P251