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Osteogenic differentiation of human periodontal ligament stem cells (PDLSCs) facilitates the neogenesis of alveolar bone and contribute to the alveolar bone repair. Calcitonin (CT) has been reported to promote osteogenic differentiation in osteoblast, but its effects and mechanism on human PDLSCs remain obscure. In this study, alizarin red staining and western blot were used to evaluate the osteogenic differentiation and the expression level of cAMP-response element-binding protein (CREB), phosphorylated CREB (pCREB), and osteopontin (OPN) in human PDLSCs. The transcriptional regulation of CREB on OPN expression was detected by chromatin immunoprecipitation (ChIP) and luciferase reporter assays. In human PDLSCs, CT overexpression significantly enhanced the expression of OPN and strengthened the mineralization, and upregulated the expression level of CREB and pCREB. The mineralized deposit and expression of OPN promoted by CT were reduced by inhibiting the expression or activity of CREB. CREB could directly bind to OPN promoter and transcriptionally regulate OPN expression. Inhibiting the expression of OPN reversed the cell osteogenic differentiation promoted by CREB. Our study supports that CT can promote osteogenic differentiation of human PDLSCs through enhancing the expression and phosphorylation of CREB, subsequently transcriptionally regulating OPN expressions.
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http://dx.doi.org/10.1007/s10266-025-01164-8 | DOI Listing |
J Clin Periodontol
September 2025
Central Laboratory, Peking University School and Hospital of Stomatology, Beijing, China.
Aim: To investigate the functional significance of mitophagy in age-related osteogenic decline and the underlying mechanisms using in vivo and in vitro models.
Materials And Methods: An alveolar bone defect model in aged mice and a serial passaging-induced ageing model of human periodontal ligament stem cells (PDLSCs) were established. Osteogenic potential in mice was assessed by micro-CT, immunofluorescence, immunohistochemical analyses and histological staining.
Int Dent J
September 2025
Dept. of Oral Implantology, the Affiliated Stomatology Hospital of Kunming Medical University, Kunming, China. Electronic address:
Objectives: Demineralised dentin matrix (DDM) is an effective scaffold material for bone tissue engineering. However, the osteoimmunological mechanism of DDM remains unexplored. Th17/Treg cell balance has been noticed as a crucial factor in bone regeneration.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Research Center for Nano-Biomaterial, Analytical and Testing Center, Sichuan University, Chengdu 610065, China.
Regeneration of infected bone defects (IBDs) requires biomaterials capable of dynamically coordinating antimicrobial, anti-inflammatory, and osteogenic functions. Overcoming the spatiotemporal mismatches in treating IBDs remains a critical challenge. Here, we designed a temporally controlled therapy based on gelatin methacrylate (GelMA)-based nanocomposite hydrogels (GCS) coembedded with sulfur quantum dots (SQDs) nanoenzymes and calcium-phosphorus oligomers (CPOs.
View Article and Find Full Text PDFExp Cell Res
September 2025
State Key Laboratory of Oral Diseases, National Center for Stomatology, National Clinical Research Center for Oral Diseases, Department of Oral and Maxillofacial Surgery, West China Hospital of Stomatology, Sichuan University, Chengdu City 610041, China. Electronic address:
Adipose-derived mesenchymal stem cells (ADSCs) hold great promise for bone tissue repair and regeneration. Circular RNAs (circRNAs) play a crucial role in regulating the osteogenic differentiation and bone remodeling of ADSCs; however, the underlying molecular mechanisms remain unclear. In this study, we conducted whole transcriptome sequencing (WTS) on ADSCs and constructed a competing endogenous RNA (ceRNA) regulatory network to identify the circTTC3/miR-205/mothers against decapentaplegic homolog 3 (Smad3) signaling axis.
View Article and Find Full Text PDFInjury
August 2025
Department of Trauma Surgery, University and University Hospital of Zurich, Raemistr. 100, 8091 Zurich, Switzerland; Center for Preclinical Development, University and University Hospital of Zurich, Raemistr. 100, 8091 Zurich, Switzerland. Electronic address:
Background: Critical size bone defects represent a clinical challenge, associated with considerable morbidity, and frequently trigger the requirement of secondary procedure. To fill osseous gaps, multiple steps are required, such as proliferation and differentiation on the cellular level and the building of extracellular matrix. In addition, the osteogenic potential of cell-derived extracellular matrices (CD-ECM) is known to enhance bone healing.
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