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Objective The purpose of this study was to evaluate the effect of immediate and delayed post space preparation on the sealing ability of two root canal obturation techniques by using micro-computed tomography imaging and a push-out test. Methods The root canals of 40 human maxillary premolar teeth were instrumented and divided into four groups: (A) single cone (SC) followed by immediate post space preparation, (B) continuous wave of condensation (CWC) followed by immediate post space preparation, (C) SC followed by delayed post space preparation, and (D) CWC followed by delayed post space preparation. Micro-CT scans were performed for volumetric analysis of voids and filling materials in the apical 4-mm portion. A push-out test was performed, and failure modes (adhesive, cohesive, or mixed) were assessed. Data were analyzed using the Kruskal-Wallis test and one-way analysis of variance. Results No significant differences were observed among the four groups in terms of the percentage volume of voids of the apical 4 mm or the bond strength of apical gutta-percha. Conclusions The percentage volume of voids and bond strength of apical gutta-percha were similar and were not significantly influenced by the timing of post space preparation or the obturation technique.

Circular RNAs (circRNAs) are novel noncoding RNAs and play crucial roles in various biological processes. However, little is known about the functions of circRNAs in osteogenic differentiation. The current study aimed to investigate the differential expression of circRNAs in rat dental follicle cells (rDFCs) during osteogenic differentiation, identified by RNA high-throughput sequencing and quantitative real-time polymerase chain reaction. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses were performed to further explore the biofunctions of circRNA biofunctions. Two hundred sixtysix differentially-expressed circRNAs that are involved in several important signaling pathways, including mitogen-activated protein kinases (MAPK) and transforming growth factor-β (TGF-β) signaling pathways were revealed. Among these, circFgfr2 and its predicted downstream targets, miR-133 and BMP6 (bone morphogenetic protein-6), were identified both in vivo and in vitro. For further validation, circFgfr2 was overexpressed in rDFCs, the results showed that the expression of miR-133 was downregulated and the expression of BMP6 was upregulated. Taken together, the results revealed the circRNA expression profiles and indicated the importance of circRNAs of rDFCs. In addition, circFgfr2 might promote osteogenesis by controlling miR-133/BMP6, which is a potential new target for the manipulation of tooth regeneration and bone formation. K E Y W O R D SGene Ontology, high-throughput sequencing, mitogen-activated protein kinase signaling system, microRNAs, osteogenesis