To investigate the effect of transforming growth factor-β3 (TGF-β3) and dental pulp stem cells (DPSC) in promoting the implant's osteointegration. Thirty-three New Zealand white rabbits were randomly divided into phosphate buffer saline (PBS) group, DPSC group and TGF-β3 + DPSC group (12 rabbits/group). Two teeth from the rabbits's mandibular incisors or molars were pulled out randomly, then implant were placed in the tooth extraction site immediately. In PBS group, the implant area was filled with Bio-Oss powder 0.30 g mixed by PBS 20 μl only; while the implant area was filled with Bio-oss powder 0.30 g and 1×10(8)/L DPSC 20 μl in DPSC group; in the the TGF-β3+DPSC group the implant area was filled with Bio-Oss powder 0.30 g mixed with 1×10(8)/L DPSC 20 μl and 80 μg/L TGF-β3 20 μl. Eighteen New Zealand rabbits were executed in the 4 weeks and 8 weeks respectively. The treated alveolar bone tissue and implant were collected for plastic section. Alizarin red staining (ARS), immunohistochemical detection (IHC) of bone sialoprotein (BSP), osteocalcin (OC) and type Ⅰ collagen (COL-Ⅰ) were performed after 4 weeks and 8 weeks. Combined bone lamelta width (CBLW) and implant bone contact rate (IBCR), trabecular width (TW) and trabecular area percentage (TA) were observed by histomorphometric measurement. ARS staining: 4 weeks after the operation, the TGF-β3+ DPSC group showed more red calcified nodules than the other two groups; 8 weeks after operation, the red calcified nodule was further increased. 4 weeks after the operation, the expression of BSP, OC and COL-Ⅰ was (0.35± 0.04), (0.36 ± 0.03) and (0.39 ± 0.01) respectively in TGF-β3+ DPSC group, (0.27 ± 0.02), (0.24 ± 0.01) and (0.28±0.03) respectively in DPSC group, and (0.13±0.03), (0.15±0.02) and (0.16±0.02) respectively in PBS group. Eight weeks after operation, the expression of BSP, OC and COL-Ⅰ was (0.51±0.02), (0.49±0.03) and (0.53±0.02) respectively in TGF-β3+DPSC group, (0.35±0.02), (0.37±0.01) and (0.38±0.01) respectively in DPSC group, and (0.21±0.03), (0.19±0.01) and (0.22±0.02) respectively in PBS group. After 4 weeks and 8 weeks, the expression of BSP, OC and COL-Ⅰ in TGF-β3+DPSC group were significantly higher than the other groups (0.05), there was no significant difference between DPSC group and PBS group (0.05). Eight weeks after operation, the CBLW, IBCR, TW and TA around implant in TGF-β3+ DPSC group were significantly higher than that in the other groups (0.05), there was no significant difference between DPSC group and PBS group (0.05). The DPSC has the potential osteogenic differentiation ability; TGF-β3 can accelerate the osteogenic differentiation of DPSC to some extent; TGF-β3 combined with DPSC can effectively promote the implant's osseointegration.
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http://dx.doi.org/10.3760/cma.j.issn.1002-0098.2017.06.009 | DOI Listing |
J Oral Biol Craniofac Res
February 2025
Department of Oral and Maxillofacial Pathology and Microbiology, KLE V K Institute of Dental Sciences, KLE Academy of Higher Education and Research, Belagavi, India.
Background: Oral submucous fibrosis (OSMF) is a chronic, potentially malignant disorder associated with areca nut consumption. It is characterized by progressive fibrosis, trismus, and a significant risk of malignancy, with limited treatment options primarily offering symptomatic relief. Dental pulp stem cells (DPSCs), a type of mesenchymal stem cells (MSCs), have shown potential for modulating fibrotic conditions through their immunomodulatory and regenerative properties.
View Article and Find Full Text PDFJ Indian Soc Periodontol
January 2025
Department of Periodontology, Bharati Vidyapeeth (Deemed to be University) Dental college and Hospital, Pimpri, Pune, Maharashtra, India.
Background: In comparison with perfectly machined surface implants, surface topographic modifications like roughness accelerate the osteogenesis of dental pulpal stem cells (DPSC). This greatly enhances bone-implant contact and osteogenic potential of the stem cells. Hence, the aim of the current study was to evaluate and compare the differentiation and proliferation potential of stem cells obtained from dental pulp on sand-blasted and acid etched implant discs surfaces.
View Article and Find Full Text PDFJ Mol Histol
February 2025
Department of Endodontics, The First Affiliated Hospital of Harbin Medical University, 143 Yiman Street, St Nangang Dist., Harbin, 150001, China.
Dental pulp stem cells (DPSCs), a subset of tooth-derived mesenchymal stem cells (MSCs), demonstrate significant promise in clinical stem cell therapy. However, prolonged in vitro expansion commonly results in compromised stemness, limiting therapeutic efficacy. Thus, maintaining the stemness of DPSCs during expansion and culture is a key challenge for regenerative medicine.
View Article and Find Full Text PDFBiochem Biophys Res Commun
March 2025
Laboratory of Molecular Genetics, Dental Research Institute, School of Dentistry, Seoul National University, Seoul, 03080, South Korea. Electronic address:
HERS/ERM cells constitute the only dental epithelial population that can be isolated from adult human teeth. Although HERS/ERM cells are the most studied dental epithelial cell source, information on their differentiation is lacking: these cells have a long induction period and low mineralization without coculture with dental mesenchymal stem cells. To characterize and develop an effective method for differentiating dental epithelial cells, we observed the epithelial‒mesenchymal interaction effects of deciduous dental pulp stem cell (dDPSC)-derived conditioned media (CM) during HERS/ERM cell differentiation.
View Article and Find Full Text PDFJ Prosthodont Res
February 2025
Department of Removable Prosthodontics, School of Dentistry, Aichi Gakuin University, Nagoya, Japan.
Purpose: Spark-discharged anodic oxidation coating on commercially pure titanium (SAc.p.Ti) has been shown to promote bone conduction and bone matrix mineralization during new bone formation.
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