Effect of titanium surface topographies on human bone marrow stem cells differentiation in vitro.

Coating characteristics of dental implants such as composition and topography regulate cell response during implant healing. The aim of this study was to assess how surface topography can affect osteogenic differentiation of mesenchymal stem cells (MSCs) by analyzing the expression levels of bone-related genes and MSCs marker. Thirty disk-shaped, commercially pure Grade 2 titanium samples (10 × 2 mm) with 3 different surface topographies (DENTSPLY-Friadent GmbH, Mannheim, Germany) were used in the present study: 10 Ti machined disks (control), 10 Ti sandblasted and acid-etched disks (DPS(®)) and 10 sandblasted and acid-etched disks at high temperature (Plus(®)). Samples were processed for real-time reverse transcription-polymerase chain reaction (RT-PCR) analysis. By comparing machined and Plus(®) disks, quantitative real-time RT-PCR showed a significant reduction of the bone-related genes osteocalcin (BGLAP) and osteoblast transcriptional factor (RUNX2). The comparison between DPS(®) and Plus(®) disks showed a slight induction of all the genes examined (RUNX2, ALPL, COL1A1, COL3A1, ENG, FOSL1, SPP1, and SP7); only the expression of BGLAP remained stable. The present study, demonstrated that implant surface topography affects osteoblast gene expression. Indeed, Plus(®) surface produces an effect on MSCs in the late differentiation stages.

A simplified post preparation technique after Thermafil obturation: evaluation of apical microleakage and presence of voids using methylene blue dye penetration.

AIM: To evaluate the apical microleakage of Thermafil obturations after three different post space preparation techniques. MATERIALS AND METHODS: 33 root canals of mono-radiculated extracted teeth were prepared with M two and then obturated with Thermafil. Teeth so treated were then divided into three groups and the post space to middle root was prepared using three different techniques. In samples in group A the housing for the post was created using a Torpan bur, and the carrier was partially removed only in the coronal portion. In samples in group B the carrier was completely removed and gutta-percha was hand compacted, before canal preparation using a Torpan bur. In samples in group C the carrier was completely removed, without guttapercha compaction, before canal preparation using a Torpan bur. The roots were immersed for 72 hours in methylene blue dye solution and sectioned transversely at 1-3-5 mm from the apex for evaluation of dye penetration using a stereomicroscope. The data collected were processed using Win CAD software and subjected to statistical analysis using the Student t test for p<0.05. RESULTS: There were no significant differences between the three groups, except for the presence of voids in the intermediate section of teeth in groups B and C. CONCLUSIONS: Post space preparation did not influence the apical seal, and gutta-percha without voids was always found in the last millimetre of the canal obturation. This study proposes a post preparation technique which provides for complete carrier removal using pliers, hand compaction of residual gutta-percha with a manual plugger and enlargement of the root canal, using appropriate post space burs, free of any interference from the carrier. Operating time is reduced, as is the risk of creating ledges or iatrogenic perforations.

Diphenylhydantoin plays a role in gene expression related to cytoskeleton and protein adhesion in human normal palate fibroblasts.

AIMS: Morphogenetic processes during palate development are related to extracellular matrix composition. The cell-extracellular matrix relation plays a role in cell activity and in gene expression. We studied the effect of diphenylhydantoin, a teratogen known to induce cleft palate in human newborns, on extracellular matrix production. We investigated whether diphenylhydantoin treatment caused any differences in glycosaminoglycans, collagen synthesis and gene expression in human normal palate fibroblasts. METHODS: Human palate fibroblasts were maintained for 24 hours in serum-free 199 medium containing 5 microg/mL (3)H-glucosamine or (3)H proline hydrochloride. Collagen and glycosaminoglycan classes were then measured using biochemical methods, gene expression with microarray analysis and cytoskeleton components with immunofluorescent antibodies and computer analysis. RESULTS: In normal fibroblasts diphenylhydantoin reduced collagen and glycosaminoglycan synthesis with a marked effect on sulphated glycosaminoglycans. There were also substantial decreases in tubulin, vimentin and alpha-actin staining and an increase of vinculin compared to controls. Diphenylhydantoin acted on several genes related to the synthesis of cytoskeleton and adhesion membrane proteins. It inhibited caderin, caveolin, RTK and alpha-actin, and increased nectin, cytoplasmatic FRG vinculin, ITGA, ITGB extracellular matrix ligand and EDG2 gene expression. DNA binding gene expression, which plays a role in cell growth and senescence, was activated. CONCLUSIONS: Since cell activity is dependent on the cell morphology and extracellular matrix composition, these findings indicate that in human normal palate fibroblasts diphenylhydantoin can modify cytoskeletal components and extracellular matrix-cell adhesion, with consequent effects on gene expression. These changes might be related to anomalous palate development.