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In Vitro Investigation of Canine Periodontal Ligament-Derived Mesenchymal Stem Cells: A Possibility of Promising Tool for Periodontal Regeneration Publisher



Salari Sedigh H1 ; Saffarpour A3 ; Jamshidi S2 ; Ashouri M4 ; Nassiri SM5 ; Dehghan MM6 ; Ranjbar E7 ; Shafieian R7, 8
Authors
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Authors Affiliations
  1. 1. Department of Clinical Sciences, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran
  2. 2. Department of Clinical Sciences, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran
  3. 3. Department of Periodontology, Tehran University of Medical Sciences, International Campus, Tehran, Iran
  4. 4. Department of Oral and Maxillofacial Pathology, Faculty of Dentistry, Shahed University of Medical Sciences, Tehran, Iran
  5. 5. Department of Clinical Pathology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran
  6. 6. Department of Surgery & Radiology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran
  7. 7. Department of Anatomy and Cell Biology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
  8. 8. Stem Cell and Regenerative Medicine Center, Mashhad University of Medical Sciences, Mashhad, Iran

Source: Journal of Oral Biology and Craniofacial Research Published:2023


Abstract

Objectives: Recent investigations indicate that canine periodontal ligament-derived stem cells (cPDLSCs) may reveal a reliable strategy for repair of periodontal tissues via cell-based tissue engineering approaches. Due to limited research, this study aimed to demonstrate the phenotypic characterization of cPDLSc in comparison with canine bone marrow-derived mesenchymal stem cells (cBMSCs) in vitro. Methods: Mesenchymal stem cells (MSCs) were obtained from PDL and BM of five male adult Mongrel dogs. In vitro isolation and expansion as well as biologic characterization including colony unit formation (CFU), osteogenic and adipogenic differentiation, flow cytometric analysis of CD34 and CD44, and RT-PCR of alkaline phosphatase (ALP), osteocalcin (OCN), periostin (POSTN) and S100A4 were performed. Furthermore, electron microscopy analysis was done to complement the comparative research. Results: CFU assay revealed that colonies of cPDLSCs presented 70% confluency with a more finite lifespan than BM-MSCs, showing a significant increase in cPDLSCs. Both types of MSCs showed osteogenic and adipogenic phenotypic characterized with clusters of mineralized depositions and lipid vacuoles, respectively. Both types of MSCs expressed CD44 with limited expression of CD34. RT-PCR of cPDLSCs revealed that expression of ALP, POSTN, OCN and S100A4 genes were significantly higher than those of BMSCs. In addition, comparison of SEM and revealed that cPDLSCs expressed more extracellular collagen fibers. Conclusions: The current study indicated that cPDLSCs show potency as a novel cellular therapy for periodontal regeneration a large animal model. © 2023
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