Effect of

Background and Objective: The 4-META/MMA-TBB (4-(2-methacryloxyethyl)trimellitic anhydride/methyl methacrylate-tributylborane) resin is widely used as a dental adhesive. It has also been applied in the dressing of gingival wound surfaces following periodontal surgery. However, its effect on the regeneration and/or cell attachment of the oral epithelium remains to be clarified. To evaluate the effect of the resin applied as wound dressing, we investigated expression of laminin 5, integrin β4 and cytokeratin 14 in regenerating oral epithelium treated with this resin following gingivectomy from the viewpoint of cell attachment and differentiation. Material and Methods: The resin was applied to the entire wound surface in rats after gingival surgery and regenerating epithelium was examined at immediately, and 1, 3, 5, 7 and 14 days later. The resin was removed 2 weeks after application in some animals and tissue further examined at 1, 3, 5 and 7 days later. Results: Regenerating epithelium under the resin was not keratinized, but became keratinized immediately after removal of the resin. Laminin 5 and integrin β4 were immunolocalized in the basal lamina, the internal basal lamina, in marginal cells of the regenerating epithelium, and at the resin-regenerating epithelium interface. Cytokeratin 14 localized in the regenerating epithelium underneath the resin, as well as in healthy and regenerated junctional epithelial cells. Conclusion: These results suggest that this resin covers the wound surface and the regenerating epithelium biologically adheres to the resin during the initial process of its regeneration. Introduction The 4-META/MMA-TBB [4-(2-methacryloxyethyl)trimellitic anhydride/methyl methacrylate-tributylborane] resin is widely employed as a dental adhesive. Numerous studies have reported its highly adhesive properties with enamel (1), dentin (1), cementum (2, 3) and bone (4, 5), and moderate biocompatibility with dentin/pulp complex (6, 7) and periodontal tissue (8). Based on the results of those studies, it has also been applied in the dressing of gingival wound surfaces following flap surgery and intentional autotransplantation of teeth (9). However, little information on its biocompatibility with epithelium is available. How it influences gingival tissue when the resin monomers deeply infiltrate surrounding tissue, and its biocompatibility with the oral mucosa during wound healing, in particular, remain to be fully clarified. Junctional epithelium can completely regenerate following gingivectomy. Experiments using rats have indicated that the oral epithelium proliferates at 2 days post-gingivectomy; the regenerating epithelium then stratifies and keratinizes, with subsequent proliferation of connective tissue. Finally, regeneration of the junctional epithelium leads to completion of gingival regeneration by adhesion to the cemento-enamel junction (CEJ) and enamel surface (10, 11). Junctional epithelium has a unique structure and function, linking the tooth surface and connective tissue, thus sealing and protecting the tooth-gingiva interface. Previous studies have demonstrated that junctional epithelium cells adhere to the tooth by hemidesmosomes and the internal basal lamina (IBL; 12-14), and by laminins, type IV collagen and proteoglycans in the extracellular matrix (ECM) of the basal lamina. Laminins have been identified in the basal lamina of junctional epithelium by immunohistochemistry and in situ hybridization. However, only laminin 5 is found in the IBL, which lacks other elements found in the ECM, including type IV collagen (15). Laminin 5, in particular, contributes to cell adhesion associated with integrin α6β4 at hemidesmosomes (16, 17). A recent research on the expression of laminin 5 and integrins in junctional epithelium demonstrated the localization of these proteins and mRNAs, which were produced by the tooth-facing cells where they contacted with the enamel surface (18). In contrast, cytokeratins (CK) are markers for the development and differentiation of epithelial tissue. CK 14, in particular, is understood to be a specific marker for junctional epithelium and the basal cells of the oral epithelium (19). It is open question how 4-META/MMA-TBB resin influences regenerating epithelium, which types of adhesive protein are concerned in the epithelium, and how the resin affects the differentiation of the regenerating epithelium following its application combined with gingivectomy. The purpose of this study was to investigate the expression of adhesive proteins (laminin 5 and integrin β4) and CK 14 following experimental gingivectomy and direct application of 4-META/MMA-TBB resin to determine the effect of this resin on regeneration of oral epithelium and cell attachment to tooth. Materials and methods Experimental design Sixty-nine male Sprague-Dawley rats (six weeks of age) were used in this study. The animals were divided into 4 groups: 18 rats each in C (Control), G (Gingivectomy), GR (Gingivectomy plus Resin application), and 12 rats in GRR (Gingivectomy plus Resin application and Removal), as described below; another 3 rats were used to investigate healthy untreated animals. All animals were deeply anesthetized by intraperitoneal injection of sodium thiopental (Ravonal, Tanabe Seiyaku, Osaka, Japan). The maxillary first and second molars on both sides of the jaw were then etched with a phosphate agent (Red Activator, Sun Medical, Moriyama, Japan) and rinsed with distilled water, after which the following treatments were performed: in the C group, 4-META/MMA-TBB resin (Super-Bond C&B, Sun Medical, Moriyama, Japan) was applied to the teeth through the neighboring palate; in the G group, the palatal gingiva, including the coronal portion of the periodontal ligament, in the first and second molar regions was removed in a 1-mm width using a fine scalpel and bleeding was staunched to maintain hemostasis; in the GR group, following gingivectomy as described for the G group, resin was applied to entire wound surface and the teeth; in the GRR group, the animals were treated in the same way as the GR group, after which the resin was removed 2 weeks later using an explorer and fine scissors, making sure to incur no bleeding. The rats were fed powdered food (Oriental Yeast, Tokyo, Japan) during the experimental period, and were sacrificed at immediately, or 1, 3, 5, 7 or 14 days after treatment in the C, G and GR groups, and at 1, 3, 5 or 7 days after removal of the resin in the GRR group. All experiments complied with the Guidelines for the Treatment of Experimental Animals at Tokyo Dental College. Histological and immunohistochemical analysis Maxillae were resected en bloc from each animal and fixed with 4% paraformaldehyde in 0.1 M phosphate buffer (pH 7.4). Specimens were infiltrated with acetone to solubilize the resin, and decalcified with 10% ethylenediaminetetraacetic acid (pH 7.2) for 2 weeks. After dehydration and paraffin embedding, the specimens were serially sectioned at 3 μm in the bucco-lingual direction and stained with hematoxylin-eosin (HE), or were used for immunohistochemistry. For immunohistochemistry, endogenous peroxidase was initially blocked with 0.3% hydrogen peroxide in methanol, after which the sections were either pretreated with 0.01% trypsin (Invitrogen, Carlsbad, CA, USA) in 50 mM Tris-HCl (pH 7.6) for 10 min at 37oC for laminin 5, or incubated in a microwave oven in 10 mM citrate (pH 6.0) for 15 min at 65oC for antigen retrieval of CK 14. The sections were then treated with 3% bovine serum albumin (BSA) to prevent non-specific binding, followed by incubation with a rabbit polyclonal antibody against laminin 5 (Abcam, Cambridge, UK; diluted 1:100) or a monoclonal antibody against CK 14 (Progen, Heidelberg, Germany; diluted 1:10). After immunoreaction with the primary antibody overnight at 4oC, the sections were then incubated with horseradish peroxidase conjugated IgG (Histofine MAX-PO (MULTI), Nichirei, Tokyo, Japan) for 30 min. Finally, they were visualized using 0.01% 3,3'-diaminobenzidine tetrahydrochloride and counterstaining with Mayer's hematoxylin. Phosphate buffered saline in place of the primary antibody was used for the negative controls. For integrin-laminin double immunofluorescence labeling, the sections were pretreated with trypsin and BSA as described above, and then immunoreacted overnight with a mixture of anti-laminin 5 (diluted 1:100) and a mouse monoclonal antibody to integrin β4 (Abcam, diluted 1:100) at 4oC. The sections were then incubated with Alexa Fluor® 488-conjugated anti-rabbit IgG (Invitrogen, Eugene, OR, USA; diluted 1:100) and Alexa Fluor® 568-conjugated anti-mouse IgG (Invitrogen; diluted 1:100) for 30 min at room temperature. Following counterstaining with 4’,6-diamino-2-phenylindole dihydrochloride (DAPI, Invitrogen), all of the specimens were examined and photographed using a conventional light/fluorescence microscope (AxioPhot 2, Carl Zeiss, Oberkochen, Germany). Results C group The keratinized layer peeled off at the surface and in the middle region of the epithelium treated with resin. Eosinophilic and amorphous materials were detected at 5 days post-operatively, but not at 7 days. No inflammatory cell infiltration was apparent in the epithelium, except for in the superficial layer and connective tissue. No distinct difference was observed between the resin-treated group and healthy untreated tissue (data not shown). Laminin 5 was expressed in the external basal lamina (EBL) and IBL of the junctional epithelium, and at the epithelium-connective tissue interface of the oral epithelium in healthy tissue. Laminin 5 expression in group C was similar to that in healthy tissue (data not shown). Intense immunoreaction for CK 14 was detected in the basal cell layer and between the enamel and junctional epithelium in the palatal gingival epithelium of healthy tissue. CK 14 was also expressed weakly in the outer cells of the junctio