Journal of Dental Research

Hypodontia, congenital absence of one or a few permanent teeth without any systemic disorders, is regarded as an autosomally inherited dominant condition with varying expression and incomplete penetrance. Many studies have reported that the prevalence of hypodontia varies from 5% to 10% among European and Asian populations. The teeth most often missing are second premolars, upper lateral incisors, and lower central incisors. Consequently, we call this trait incisor-premolar hypodontia. Peg-shaped or strongly mesio-distally reduced upper lateral incisors demonstrate variation in the expression of the trait. The gene or genes causing incisor-premolar hypodontia are not known. We have begun the genetic mapping of hypodontia by using linkage analyses in seven Finnish three-generation families with 77 individuals, 31 affected with incisor-premolar hypodontia. As the first step, we studied the possibility of linkage between hypodontia and some candidate genes which have been suggested to have important functions during tooth development. Here we report the exclusion of EGF, EGFR, and FGF-3 loci as possible sites for gene mutation causing incisor-premolar hypodontia in our family material. Because of the close location of the FGF-3 and FGF-4 genes, the results also suggest the exclusion of the FGF-4 locus.

The Fas antigen is a cell-surface glycoprotein that mediates apoptosis from the cell surface into the cytoplasm. Polyclonal antibody (Fas D) was raised against a synthetic polypeptide selected from the extracellular part of the human Fas antigen (amino acid residues 104-114) and was used to detect the Fas antigen in human gingiva. Biopsy specimens of human gingiva were prepared, and the paraffin sections were reacted with the Fas D antibody by an immunohistochemical method. The antibody localized to the prickle-cell layer and to granular layer keratinocytes of human gingiva. Proteins were also prepared from human gingiva and subjected to SDS-PAGE, followed by Western-blotting analysis with the Fas D antibody. The antibody interacted with a band corresponding to an estimated molecular weight of 35 kDa. The incidence of the immunoreactive 35-kDa protein was detected in the gingiva of 90% of the 20 individuals examined. The Fas antigen detected in human gingiva may be related to the physiological turnover of oral mucosa.

Intra-oral wounds, like wounds in children, demonstrate privileged healing when compared with adult wounds at extra-oral sites. This study investigated whether this preferential healing is related to an increased ability of oral mucosal fibroblasts to reorganize extracellular matrix (ECM) when compared with their dermal counterparts. ECM reorganization was investigated by means of a fibroblast-populated collagen lattice (FPCL) system. The effect of donor age was also investigated in this system. Differences in ECM reorganization and FPCL contraction were evident: FPCL contraction was more rapid by oral mucosal fibroblasts than dermal fibroblasts (p < 0.01). FPCL contraction was also greater in child (donor < 10 years) than adult (donor > 18 years) oral mucosal fibroblasts (p < 0.01). These differences were not related to phenotypic differences in cell viability (p > 0.5), DNA synthesis (p > 0.05), and cell number (p > 0.5) within the FPCLs, or cellular attachment to collagen (p > 0.07). FPCL contraction was not stimulated by the addition of conditioned medium from oral mucosal or dermal fibroblasts (p > 0.05). These data show that the significantly increased ability of oral mucosal fibroblasts to reorganize ECM in vitro, when compared with dermal fibroblasts, represents a distinct phenotypic contractile difference, rather than differences in their production of soluble mediators or cell attachment to ECM.

When condylar cartilage is maintained under non-functional organ culture conditions, its phenotypic expression is altered to a premature form with less expression of the type II collagen characteristic of mature chondroblasts. The aim of this study was to examine whether, by electrical stimulation of the major masticatory muscle, the masseter muscle, chondrogenic expression could be maintained under organ culture conditions in which the jaws with the craniomandibular joint were cultured in one block. Sixty BALB/c mice of both sexes were divided randomly into three groups of equal size. Two groups were decapitated at the age of 5 days. The cranial base and mandible were dissected out in one block, and the explant was placed on its cut surface on a culture dish. The masseter muscles of the explants in one group were stimulated with an electric pulsing device delivering an AC current of a frequency of 0.7 Hz and an amplitude of 5V with hourly active and silent periods. Five experimental and five control explants were fixed after culture periods of 1, 3, 7, and 14 days. The mice in the third group were used as in vivo controls. By electrical stimulation of the masseter muscle, the phenotypic characteristics of the condylar chondroblasts, such as the deposition of type II collagen and the thickness of the cartilage layers, closely resembled the situation in vivo, while the controls in a non-functional environment gradually lost their characteristic form.

Long-face subjects have strongly reduced bite forces relative to normal subjects. This difference cannot be fully explained by the reduced cross-sectional area of the jaw muscles. In this study, we investigated whether the orientation and moment arms of the jaw muscles of normal and long-face subjects are different, and if so, to what extent these differences contribute to the observed differences in maximum molar bite-force levels. Three MRI scan series with different orientations were made of the jaw muscles of 30 normal and 13 long-face subjects. These served as the basis for computer reconstructions of the external shape of the muscles. The spatial orientation of the jaw muscles was defined by the regression line through the centroids of the muscular cross-sections. The moment arms of the jaw muscles and the bite point of the first mandibular molar were measured with respect to the center of the ipsilateral condyle. The muscular variables-including angles, moment arms, and mechanical advantage-were analyzed with a discriminant analysis and a multivariate analysis of variance (MANOVA). Differences in the spatial orientation of the temporalis muscle and the anterior digastric muscle contributed most to the distinction of the normal and long-face group. With MANOVA, it was shown that the normal and long-face group did not significantly differ with respect to the jaw muscle moment arms and mechanical advantage data. Only small differences were found between the sagittal muscle angles of the masseter and anterior digastric muscles in the two groups. In both the normal and long-face group, the orientation and moment arm data of the right and left muscles differed significantly. It was concluded that the variation of the spatial orientation of the jaw muscles is small and does not significantly contribute to the explanation of the different molar bite-force levels of long-face and normal subjects. Therefore, it is tempting to assume that the jaw muscles of normal and long-face subjects are different with respect to the maximum force they can exert per unit of cross-sectional area.

Non-collagenous proteins of dentin and bone have important effects on mineralization which have been studied by various in vitro systems. We developed an in vitro mineralization system using electrophoretic gels as diffusion media of calcium and phosphate ions. Calcium and phosphate ions were diffused naturally or propelled by electric potential. Calcium phosphate was precipitated in the gel, and the precipitation was affected by proteins in the gel which had been separated by electrophoresis. We applied this system to analysis of non-collagenous proteins of dentin. Among the proteins, phosphophoryns promoted calcium phosphate precipitation in the natural-diffusion system. A non-collagenous protein having a molecular mass of 60 kDa inhibited precipitation. The results were different, however, in the electric-diffusion system, in which phosphophoryns had a negative effect. The present system enabled us to compare the effects of plural proteins rapidly, even using unpurified material.

Laser irradiation alters the structure of dentin and produces surface layers that give the appearance of being more enamel-like. The laser-modified surface may be more resistant to demineralization; hence, many investigators are proposing continued development of the laser as a possible preventive treatment for caries. The purpose of this study was to explore the morphological changes that occur in dentin when treated at threshold illuminance with two clinically interesting laser wavelengths, and to evaluate the effectiveness of the laser-treated surface at resisting demineralization in an acid-gel solution. The Nd:YAG laser (wavelength 1060 nm) produced significant recrystallization and grain growth of the apatite, without the formation of second phases such as β-tricalcium phosphate. This recrystallized surface layer showed resistance to demineralization; however, the layer did not provide protection of the underlying dentin from demineralization because of cracks and macroscopic voids that allowed for penetration of the demineralizing gel. The Ho:YAG laser-treated surface (wavelength 2100 nm) did not show significant evidence of recrystallization and grain growth, and only a trace amount of an acid-resistant layer was observed with demineralization. It is speculated that the Ho:YAG laser is coupling with absorbed water, and that the heat transfer from the water to the mineral phase is inefficient. For the purposes of creating a demineralization-resistant layer, threshold illuminance with both Nd:YAG and Ho:YAG was ineffective.

Previous studies have suggested minor differences between primary and permanent teeth in terms of dentin composition and morphology. Other reports indicated lower bond strengths of resin composites to dentin of primary teeth compared with dentin of permanent teeth; however, no information is available regarding differences in the micromorphology of the resin-dentin interface that may explain these lower bond strengths. Therefore, the purpose of the present study was to compare primary and permanent teeth in terms of the thickness of the hybrid layer developed with two bonding systems. Our hypothesis was that bonding differences previously reported between primary and permanent dentin would be reflected in hybrid layer differences observable in SEM analyses. Twenty human extracted and non-carious teeth were divided into 4 groups: 5 primary and 5 permanent teeth restored with All-Bond 2/Bisfil P system; and 5 primary and 5 permanent teeth restored with Scotchbond Multi-Purpose/ZlOO. The sample area available on each tooth was divided for the two dentin conditioning times (7 and 15 sec). Measurements of hybrid layer thickness were performed by means of SEM at xl3,000. The results of this study indicated that the hybrid layer produced is significantly thicker in primary than in permanent teeth (p = 0.0001), suggesting that primary tooth dentin is more reactive to acid conditioning. No difference was observed in the hybrid layers produced by the two adhesive systems (p = 0.7920). The increased thickness of the hybrid layer in primary teeth (25 to 30%) and the subsequent lack of complete penetration of adhesive resin into previously demineralized dentin may contribute to the lower bond strengths to primary dentin reported in the literature. If a narrower hybrid layer more uniformly infused with resin is the goal of dentin bonding, it is concluded that a differentiated protocol for bonding to primary dentin (with shorter time for dentin conditioning) can be used as a means to reproduce the hybrid layer thickness seen in permanent teeth.

The regional bond strengths of three current-generation bonding systems (All Bond 2, Scotchbond MultiPurpose, and Clearfil Liner Bond 2) were measured in natural wedge-shaped defects in the cervical area of extracted human teeth. A microtensile testing method was used to compare the strengths of resin bonds made to occlusal margins with those made to gingival margins. Controls consisted of normal teeth which had artificial wedge-shaped defects, of the same depth and dimension, created with a high-speed bur. The results indicated that there were no regional differences in bond strength, although bonds made to natural lesions were from 20 to 45% lower than those made to normal dentin in artificially created wedge-shaped defects, depending on the bonding agent. Scanning electron microscopy revealed that Clearfil Liner Bond 2 created the thinnest hybrid layers, which were difficult to measure in the natural lesions. The natural lesions contained sclerotic dentin, whereas the artificial lesions were composed of normal dentin. Although the bond strengths to sclerotic dentin were lower than those to normal dentin, the absolute values (ca. 16 to 17 MPa) were high relative to previous-generation bonding agents.

The functional surfaces of porcelain restorations are often ground to adjust occlusion. This removes the surface glaze and introduces flaws. Re-firing the restoration before final placement produces a self-glaze layer on the surface that may reduce the extent of damage caused by grinding. The objectives of this study were to determine whether re-firing after grinding increases the strength of dental porcelain and to determine whether the effectiveness of this treatment was dependent on the initial flaw size. Six groups, each containing 12 disk specimens, were prepared from experimental body porcelain (No. 36, J.F. Jelenko & Co., Armonk, NY). The specimens were fired under vacuum, ground to a thickness of 1 mm with 240-grit SiC abrasive, and polished through 600-grit on the surface to be subjected to tensile stress. Control Group A consisted of 12 non-indented specimens. Flaws were induced in the remaining groups by means of a Vickers indenter under the following loads: 3.9 N (Group B), 7.8 N (Group C), 11.8 N (Group D), 15.7 N (Group E), and 19.6 N (Group F). Following indentation, half of the specimens from each group were re-fired. The flexure strength of each specimen was determined by means of a piston-on-three-ball biaxial fixture. The TTEST procedure of SAS (1985) indicated a significant difference between the mean strength values of glazed and non-glazed specimens in Group E only (p = 0.55, 0.24, 0.13, 0.07, 0.01, and 0.69 for Groups A to F, respectively). ANOVA with the GLM procedure of SAS (1985) revealed that the mean strength values of groups subjected to five indentation loads were not significantly different (p = 0.45 for glazed specimens and p = 1.00 for non-glazed specimens). These findings support those of Fairhurst et al. (1992) for specimens with smaller flaws that were induced by grinding with 1 um abrasive grit. The results of the current study indicate that re-firing of porcelain with large surface flaws does not significantly increase the flexural strength.

The use of citric acid is efficacious and distinctive in the demineralization of dentinal root surfaces for periodontal regeneration and in the etching and conditioning of enamel or dentin for bonding restorative resins. To decipher the role of citric acid in these applications, it is important that one have a basic understanding of its interaction with synthetic hydroxyapatite. The uptake or removal of citrate ions from aqueous solutions of citric acid (4 to 100 mmol/L, 10 mL) by hydroxyapatite (1 g) was studied at 22°C after a given reaction period (from 3 hr to 11 days) by immediate spectrophotometric monitoring of the concentrations of the filtrates (214 nm). The concentrations of calcium, phosphate, and hydrogen ions were also determined in the same solutions. The interaction: (i) is a time-independent ionic-exchange process with the substrate when the initial acid concentrations are dilute (4 to 12.5 mmol/L), and (ii) is a reactive process that is time-dependent for higher acid concentrations. The exchange process shows an adsorption of about one citrate ion per (100) face of the unit cell of hydroxyapatite for a maximally exchanged surface. The curves representing the reactive process may be quantitatively or qualitatively explained on the basis of the supersaturation of the solutions with respect to calcium citrate and its slow precipitation. The physico-chemical analysis of the needle-shaped birefringent crystals of the precipitate from the supersaturated solutions confirms the precipitate to be Ca₃(citrate) ₂·4H₂O.