Effects of critical thermal cycling on the flexural strength of resin composites.

We compared flexural strength (FS) in four resin composites before and after three protocols for thermal cycling aging. Four resin composites were evaluated: Enamel Plus Hri, Gradia Direct Posterior, Grandioso, and Grandioso Flow. Sixty specimens (2 × 2 × 25 mm) were fabricated using a split metallic mold and light-cured for 30 s. The specimens were then randomly divided into four groups and tested using one of the following thermal cycling procedures: (1) storage in deionized water for 24 h (control group), (2) 15,000 cycles, 3) 30,000 cycles, and 4) 45,000 cycles. Each thermal cycling procedure was conducted between 5 °C and 55 °C, with a dwell time of 30 s. All specimens were subjected to a three-point bending test, to determine FS (0.5 mm/min). "Material" and "thermal aging" were significantly associated with FS (P < 0.001). A statistically significant interaction between the two factors was also detected (P < 0.001). In the non-aged groups, nanohybrid composites had the highest FS. FS significantly decreased after thermal cycling protocols in all composites tested. Gradia composite exhibited decrease in FS only after 45,000 cycles. In contrast, FS significantly decreased in the Grandioso Flow composite at 15,000 cycles. The trend in the decrease varied among composites, and the decrement in FS was not proportional to baseline values.

Effect of different irrigating solutions and endodontic sealers on bond strength of the dentin-post interface with and without defects.

AIMS: To investigate how the interfacial shear strength of the dentin-post interface with and without defects changes for different combinations irrigant/sealer. METHODS: In forty human decoronated and instrumented teeth, fibreglass posts were inserted. The obtained root segments were randomly assigned to four different groups according to the irrigant adopted and the cement used to seal the root canal. The root segments were processed for metyl-methacrylate embedding. Serial sections were obtained and submitted to histomorphometric analyses in order to observe any defect of adhesion at the dentin-post interface and to measure the defects' dimension. The serial sections were also submitted to micro-push-out test. The measured shear strength values were subjected to statistical analysis by one-way ANOVA. The values of bond strength determined for the defective samples were correlated with the dimension of the defects. Finite element models were built to interpret and corroborate the experimental findings. RESULTS: ANOVA showed that the generic combination irrigant/sealer does not affect the interfacial shear strength values. The bond strength of the samples without defects was averagely twice as large as that of the defective samples. The defects occupying more than 12% of the total transverse section area of the endodontic cement layer led to a reduction of the bond strength of about 70%. The predictions of the finite element models were in agreement with the experimental results. CONCLUSION: Defects occupying less than 2% of the total transverse section area of the cement layer were shown to be acceptable as they have rather negligible effects on the shear strength values. Technologies/protocols should be developed to minimize the number and the size of the defects.

Osteogenic differentiation of dental follicle stem cells.

BACKGROUND: Stem cells are defined as clonogenic cells capable of self-renewal and multi-lineage differentiation. A population of these cells has been identified in human Dental Follicle (DF). Dental Follicle Stem Cells (DFSCs) were found in pediatric unerupted wisdom teeth and have been shown to differentiate, under particular conditions, into various cell types of the mesenchymal tissues. AIM: The aim of this study was to investigate if cells isolated from DF show stem features, differentiate toward osteoblastic phenotype and express osteoblastic markers. METHODS: We studied the immunophenotype of DFSCs by flow cytometric analysis, the osteoblastic markers of differentiated DFSCs were assayed by histochemical methods and real-time PCR. RESULTS: We demonstrated that DFSCs expressed a heterogeneous assortment of makers associated with stemness. Moreover DFSCs differentiated into osteoblast-like cells, producing mineralized matrix nodules and expressed the typical osteoblastic markers, Alkaline Phosphatase (ALP) and Collagen I (Coll I). CONCLUSION: This study suggests that DFSCs may provide a cell source for tissue engineering of bone.

TRAIL is involved in human osteoclast apoptosis.

Control of osteoclast (OC) apoptosis has been recognized as a critical regulatory factor in bone remodeling. TRAIL, a member of the TNF superfamily, induces apoptosis in neoplastic and normal cells. However, few data are available on the effects of TRAIL on bone cells, thus in the present study we investigated TRAIL role on the apoptosis of human mature OCs. We show that TRAIL treatment causes reduced cell viability, loss of nuclei integrity, and derangement of the actin microfilament in OCs. We also demonstrated that the death receptor DR5, upregulated by TRAIL, could be the mediator of TRAIL-induced OC apoptosis.