Osteogenic potency of dental stem cell-composite scaffolds in an animal cleft palate model
2
Issued Date
2024-08-30
Resource Type
eISSN
24058440
Scopus ID
2-s2.0-85201114392
Journal Title
Heliyon
Volume
10
Issue
16
Rights Holder(s)
SCOPUS
Bibliographic Citation
Heliyon Vol.10 No.16 (2024)
Suggested Citation
Rattanapinyopituk K., Chaweewannakorn C., Tangjit N., Dechkunakorn S., Anuwongnukroh N., Sritanaudomchai H. Osteogenic potency of dental stem cell-composite scaffolds in an animal cleft palate model. Heliyon Vol.10 No.16 (2024). doi:10.1016/j.heliyon.2024.e36036 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/100568
Title
Osteogenic potency of dental stem cell-composite scaffolds in an animal cleft palate model
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Corresponding Author(s)
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Abstract
Objective: To evaluate the osteogenic potency of stem cells isolated from human exfoliated deciduous teeth (SHED) in polycaprolactone with gelatin surface modification (PCL-GE) and poly (lactic-co-glycolic acid)-bioactive glass composite (PLGA-bioactive glass (BG)) scaffolds after implantation in a rat cleft model. Methods: Cleft palate-like lesions were induced in Sprague-Dawley rats by extracting the right maxillary first molars and drilling the intact alveolar bone. Rats were then divided into five groups: Control, PCL-GE, PCL-GE-SHED, PLGA-BG, and PLGA-BG-SHED, and received corresponding composite scaffolds with/without SHED at the extraction site. Tissue samples were collected at 2, 3, and 6 months post-implantation (4 rats per group). Gross and histological analyses were conducted to assess osteoid or bone formation. Immunohistochemistry for osteocalcin and human mitochondria was performed to evaluate bone components and human stem cell viability in the tissue. Results: Bone tissue formation was observed in the PCL-GE and PLGA-BG groups compared to the control, where no bone formation occurred. PLGA-BG scaffolds demonstrated greater bone regeneration potential than PCL-GE over 2–6 months. Additionally, scaffolds with SHED accelerated bone formation compared to scaffolds alone. Osteocalcin expression was detected in all rats, and positive immunoreactivity for human mitochondria was observed in the regenerated bone tissue with PCL-GE-SHED and PLGA-BG-SHED. Conclusion: PCL-GE and PLGA-BG composite scaffolds effectively repaired and regenerated bone tissue in rat cleft palate defects. Moreover, scaffolds supplemented with SHED exhibited enhanced osteogenic potency. Clinical significance: PCL-GE and PLGA-BG scaffolds, augmented with SHED, emerge as promising biomaterial candidates for addressing cleft repair and advancing bone tissue engineering endeavors.