Purpose: Several scaffolds and cell sources are being investigated for cartilage regeneration. The aim of the study was to prepare nanocellulose-based thermosensitive injectable hydrogel scaffolds and assess their potential as 3D scaffolds allowing the chondrogenic differentiation of embedded human dental pulp stem and progenitor cells (hDPSCs). Materials and Methods: The hydrogel-forming solutions were prepared by adding β-glycerophosphate (GP) to chitosan (CS) at different ratios. Nanocellulose (NC) suspension was produced from hemp hurd then added dropwise to the CS/GP mixture. In vitro characterization of the prepared hydrogels involved optimizing gelation and degradation time, mass-swelling ratio, and rheological properties. The hydrogel with optimal characteristics, NC-CS/GP-21, was selected for further investigation including assessment of biocompatibility. The chondrogenesis ability of hDPSCs embedded in NC-CS/GP-21 hydrogel was investigated in vitro and compared to that of bone marrow-derived mesenchymal stem cells (BMSCs), then was confirmed in vivo in 12 adult Sprague Dawley rats. Results: The selected hydrogel showed stability in culture media, had a gelation time of 2.8 minutes, showed a highly porous microstructure by scanning electron microscope, and was morphologically intact in vivo for 14 days after injection. Histological and immunohistochemical analyses and real-time PCR confirmed the chondrogenesis ability of hDPSCs embedded in NC-CS/GP-21 hydrogel. Conclusion: Our results suggest that nanocellulose–chitosan thermosensitive hydrogel is a biocompatible, injectable, mechanically stable and slowly degradable scaffold. hDPSCs embedded in NC-CS/GP-21 hydrogel is a promising, minimally invasive, stem cell-based strategy for cartilage regeneration.

Objectives Single-shade composite systems are gaining popularity among clinicians due to the claimed potential of blending with different tooth structure shades while restoring the tooth. The purpose of this study was to evaluate the blending effect of two single-shade composite with different shades of conventional resin composite systems. Materials and Methods Seventy-two composite cylinders of B1, B2, A1, A2, A3, or A3.5 shade from CharmFil Plus (CP) and Filtek Universal Restorative (3M) were prepared using custom-made silicone mold. Single-shade composite OMNICHROMA (OC) or Beautifil II Enamel (BE) was placed in the center of each cylinder and polymerized. The color parameters, lightness (L*), chroma (C*), and hue (H*) of each composite were measured using a color chronometer. Furthermore, color stability of the samples was evaluated after 1-week staining challenge. Statistical Analysis Multivariant analysis was performed to evaluate the effect of material and shade on the color parameters. Multiple comparisons of the data were performed using post hoc test. The staining challenge data were analyzed using repeated measure analysis of variance and paired sample T-test. Results The multivariant analysis showed a statistically significant difference in color parameters among CP, 3M, OC, and BE (p = 0.001). Image analysis showed a visual blending effect for both OC and BE for certain shades; however, some color contrast with the darker shades was observed. The C* value of OC showed a similar pattern to CP; however, the H* of the latter was closely followed by BE. The L* value showed statistically significant difference among the shades of 3M, and in OC and BE when blended with 3M. Conclusion All four materials used in this study showed color alteration after the staining challenge. Single-shade composite can blend with only certain shades of resin composites.

Significance: Osteoporosis is a major health problem worldwide, as the aging population is soaring. However, molecules involved in the regulation of bone remodeling are still incompletely understood. Nck (noncatalytic region of tyrosine kinase) is an adaptor molecule linking cytoskeleton and cell motility. We now identify that Nck regulates cell migration in vitro as well as in vivo and regulates bone mass via bone formation activity. Nck positively regulates repair of bone injury. This discovery provides a unique insight into the understanding of bone remodeling.