Anti-adhesive and pro-apoptotic effects of 2-hydroxyethyl methacrylate on human gingival fibroblasts co-cultured with Streptococcus mitis strains

Aim To evaluate and observe the cellular reactions that occur during the interaction/integration between 2-hydroxyethyl methacrylate/host tissue/microbial environment, in a co-culture of human gingival fibroblasts (HGF) and Streptococcus mitis strains. Methodology Streptococcus mitis were cultured with strains in the presence of 3 mmol L−1 HEMA for 48 h and 72 h. Cytotoxicity was evaluated by the trypan blue dye exclusion test. Apoptosis was evaluated by TUNEL analysis. Adhesion was evaluated by immunofluorescence and western blot analyses. Quantitative analyses of the results were acquired by Qwin Plus 3.5 and QuantityOne I-D analysis software, respectively. The statistical significance of the results was evaluated using t-tests and linear regression tests. Results The trypan blue dye test revealed 47.3% and 46.5% of dead fibroblasts after 48 and 72 h HEMA treatment, respectively, while bacterial viability was not influenced by the presence of HEMA and fibroblasts. The expression of pro-collagen I, involved in fibroblast adhesion, in untreated samples ranged from 12.49% to 6.91% of the positive area after 48 and 72 h, respectively, dropping to below 2% of the positive area in the other experimental conditions. Unlike the trypan blue test, co-cultured samples treated with HEMA showed 20% and 25% versus 17% and 21% (after 48 and 72 h, respectively) of apoptotic cells. Conclusions The evidence for HEMA toxicity and anti-adhesive effects against eukaryotic cells was reduced in the presence of bacteria, suggesting that dental resins should be well polymerized to avoid the spread of toxic monomers within the mouth.

[1]  Liu Dan,et al.  Fibroblast response to interstitial flow: A state‐of‐the‐art review , 2010, Biotechnology and bioengineering.

[2]  G. Grégoire,et al.  HEMA reactivity with demineralized dentin. , 2010, Journal of dentistry.

[3]  J. Błasiak,et al.  Genotoxicity and cytotoxicity of 2-hydroxyethyl methacrylate. , 2010, Mutation research.

[4]  W. Teughels,et al.  Microbial Interactions Influence Inflammatory Host Cell Responses , 2009, Journal of dental research.

[5]  A. Cataldi,et al.  Vascular Endothelial Growth Factor and E-Nitric Oxide Synthase-Mediated Regenerative Response Occurring upon Autologous and Heterologous Bone Grafts , 2009, International journal of immunopathology and pharmacology.

[6]  A. Ruggeri,et al.  HEMA down-regulates procollagen alpha1 type I in human gingival fibroblasts. , 2009, Journal of biomedical materials research. Part A.

[7]  R. Hickel,et al.  The toxicokinetics and distribution of 2-hydroxyethyl methacrylate in mice. , 2009, Biomaterials.

[8]  V. Miletic,et al.  Remaining unreacted methacrylate groups in resin-based composite with respect to sample preparation and storing conditions using micro-Raman spectroscopy. , 2008, Journal of biomedical materials research. Part B, Applied biomaterials.

[9]  M. Fox Novel roles for collagens in wiring the vertebrate nervous system. , 2008, Current opinion in cell biology.

[10]  Y. Uzunova,et al.  High-performance liquid chromatographic determination of unreacted monomers and other residues contained in dental composites. , 2008, Journal of biochemical and biophysical methods.

[11]  G. Matarese,et al.  Biomonitoring of DNA damage in peripheral blood lymphocytes of subjects with dental restorative fillings. , 2008, Mutation research.

[12]  G. Mazzotti,et al.  Effects of HEMA on type I collagen protein in human gingival fibroblasts , 2007, Cell Biology and Toxicology.

[13]  G. Spagnuolo,et al.  Genetic and Cellular Toxicology of Dental Resin Monomers , 2006, Journal of dental research.

[14]  G. Leyhausen,et al.  Effects of three resin monomers on the cellular glutathione concentration of cultured human gingival fibroblasts. , 2006, Dental materials : official publication of the Academy of Dental Materials.

[15]  V. D’antò,et al.  Effect of N-acetyl-L-cysteine on ROS production and cell death caused by HEMA in human primary gingival fibroblasts. , 2006, Biomaterials.

[16]  I. About,et al.  Polymerized bonding agents and the differentiation in vitro of human pulp cells into odontoblast-like cells. , 2005, Dental materials : official publication of the Academy of Dental Materials.

[17]  A. Jewett,et al.  Resin Monomer 2-Hydroxyethyl Methacrylate (HEMA) is a Potent Inducer of Apoptotic Cell Death in Human and Mouse Cells , 2005, Journal of dental research.

[18]  A. Leonardi,et al.  NF-κB Protection against Apoptosis Induced by HEMA , 2004 .

[19]  C. T. Hanks,et al.  Cytotoxic effects of current dental adhesive systems on immortalized odontoblast cell line MDPC-23. , 1999, Dental materials : official publication of the Academy of Dental Materials.

[20]  J. Wataha,et al.  In vitro cytotoxicity and dentin permeability of HEMA. , 1996, Journal of endodontics.

[21]  R. G. Craig,et al.  Setting Reactions and Compressive Strengths of Calcium Phosphate Cements , 1990, Journal of dental research.

[22]  S. Schwengberga,et al.  In vitro embryotoxicity assessment with dental restorative materials , 2005 .

[23]  D. Watts,et al.  Resin composite monomers alter MTT and LDH activity of human gingival fibroblasts in vitro. , 2004, Dental materials : official publication of the Academy of Dental Materials.

[24]  A. Leonardi,et al.  NF-kappaB protection against apoptosis induced by HEMA. , 2004, Journal of dental research.

[25]  W. Geurtsen,et al.  Biocompatibility of resin-modified filling materials. , 2000, Critical reviews in oral biology and medicine : an official publication of the American Association of Oral Biologists.

[26]  J. Wataha,et al.  The influence of dentine permeability on cytotoxicity of four dentine bonding systems, in vitro. , 1998, Journal of oral rehabilitation.

[27]  D. Pashley Dynamics of the pulpo-dentin complex. , 1996, Critical reviews in oral biology and medicine : an official publication of the American Association of Oral Biologists.