Evaluation of the regenerative capacity of stem cells combined with bone graft material and collagen matrix using a rabbit calvarial defect model
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Purpose: The purpose of this study was to evaluate the regenerative capacity of stem cells combined with bone graft material and a collagen matrix in rabbit calvarial defect models according to the type and form of the scaffolds, which included type I collagen matrix and synthetic bone. Methods: Mesenchymal stem cells (MSCs) were obtained from the periosteum of participants. Four symmetrical 6-mm-diameter circular defects were made in New Zealand white rabbits using a trephine drill. The defects were grafted with (1) group 1: synthetic bone (β-tricalcium phosphate/hydroxyapatite [β-TCP/HA]) and 1×105 MSCs; (2) group 2: collagen matrix and 1×105 MSCs; (3) group 3: β-TCP/HA, collagen matrix covering β-TCP/HA, and 1×105 MSCs; or (4) group 4: β-TCP/HA, chipped collagen matrix mixed with β-TCP/HA, and 1×105 MSCs. Cellular viability and cell migration rates were analyzed. Results: Uneventful healing was achieved in all areas where the defects were made at 4 weeks, and no signs of infection were identified during the healing period or at the time of retrieval. New bone formation was more evident in groups 3 and 4 than in the other groups. A densitometric analysis of the calvarium at 8 weeks post-surgery showed the highest values in group 3. Conclusions: This study showed that the highest regeneration was found when the stem cells were applied to synthetic bone along with a collagen matrix.
Abstract
Purpose: The purpose of this study was to evaluate the regenerative capacity of stem cells combined with bone graft material and a collagen matrix in rabbit calvarial defect models according to the type and form of the scaffolds, which included type I collagen matrix and synthetic bone. Methods: Mesenchymal stem cells (MSCs) were obtained from the periosteum of participants. Four symmetrical 6-mm-diameter circular defects were made in New Zealand white rabbits using a trephine drill. The defects were grafted with (1) group 1: synthetic bone (β-tricalcium phosphate/hydroxyapatite [β-TCP/HA]) and 1×105 MSCs; (2) group 2: collagen matrix and 1×105 MSCs; (3) group 3: β-TCP/HA, collagen matrix covering β-TCP/HA, and 1×105 MSCs; or (4) group 4: β-TCP/HA, chipped collagen matrix mixed with β-TCP/HA, and 1×105 MSCs. Cellular viability and cell migration rates were analyzed. Results: Uneventful healing was achieved in all areas where the defects were made at 4 weeks, and no signs of infection were identified during the healing period or at the time of retrieval. New bone formation was more evident in groups 3 and 4 than in the other groups. A densitometric analysis of the calvarium at 8 weeks post-surgery showed the highest values in group 3. Conclusions: This study showed that the highest regeneration was found when the stem cells were applied to synthetic bone along with a collagen matrix.
참고문헌 (27)
- Adolpho LF, "Human periodontal ligament stem cells with distinct osteogenic potential induce bone formation in rat calvaria defects", Regen Med, 17, pp.341~353 (2022)
- Ho-Shui-Ling A, "Bone regeneration strategies: engineered scaffolds, bioactive molecules and stem cells current stage and future perspectives", Biomaterials, 180, pp.143~162 (2018)
- Sui BD, "Stem cell-based bone regeneration in diseased microenvironments : challenges and solutions", Biomaterials, 196, pp.18~30 (2019)
- Zomorodian E, "Mesenchymal stem cells as a potent cell source for bone regeneration", Stem Cells Int, 2012, pp.980353~ (2012)
- Yuan Zhe Jin, "Mesenchymal Stem Cell Therapy for Bone Regeneration", Clinics in Orthopedic Surgery, 10(3), pp.271~278 (2018), 대한정형외과학회
- Wahl EA, "In vitro evaluation of scaffolds for the delivery of mesenchymal stem cells to wounds", BioMed Res Int, 2015, pp.108571~ (2015)
- Assi R, "Delivery of mesenchymal stem cells in biomimetic engineered scaffolds promotes healing of diabetic ulcers", Regen Med, 11, pp.245~260 (2016)
- Putri IL, "Alveolar repair using cancellous bone and beta tricalcium phosphate seeded with adipose-derived stem cell", Cleft Palate Craniofac J (2022)
- Almansoori AA, "Mesenchymal stem cells and platelet-rich plasma-impregnated polycaprolactone-β tricalcium phosphate bio-scaffold enhanced bone regeneration around dental implants", Int J Implant Dent, 7, pp.35~ (2021)
- Vahabi S, "A comparison between the efficacy of Bio-Oss, hydroxyapatite tricalcium phosphate and combination of mesenchymal stem cells in inducing bone regeneration", Chang Gung Med J, 35, pp.28~37 (2012)
- Shayesteh YS, "Sinus augmentation using human mesenchymal stem cells loaded into a β-tricalcium phosphate", hydroxyapatite scaffold, 2008, pp.106, 203~209
- Jafarian M, "Marrow-derived mesenchymal stem cells-directed bone regeneration in the dog mandible : a comparison between biphasic calcium phosphate and natural bone mineral", Oral Surg Oral Med Oral Pathol Oral Radiol Endod, 105, pp.e14~e24 (2008)
- 강승환, "Assessment of stem cell viability in the initial healing period in rabbits with a cranial bone defect according to the type and form of scaffold", Journal of Periodontal & Implant Science, 49(4), pp.258~267 (2019), 대한치주과학회[DOI]
- Lequeux C, "Subcutaneous fat tissue engineering using autologous adipose-derived stem cells seeded onto a collagen scaffold", Plast Reconstr Surg, 130, pp.1208~1217 (2012)
- Liu Y, "Comparison of polyglycolic acid, polycaprolactone, and collagen as scaffolds for the production of tissue engineered intestine", J Biomed Mater Res B Appl Biomater, 107, pp.750~760 (2019)
- Heffner JJ, "Bone marrow-derived mesenchymal stromal cells and platelet-rich plasma on a collagen matrix to improve fascial healing", Hernia, 16, pp.677~687 (2012)
- Lim S, "Umbilical cord mesenchymal stem cell-derived nanovesicles potentiate the bone-formation efficacy of bone morphogenetic protein 2", Int J Mol Sci, 21, pp.6425~ (2020)
- Schlund M, "Rabbit calvarial and mandibular critical-sized bone defects as an experimental model for the evaluation of craniofacial bone tissue regeneration", J Stomatol Oral Maxillofac Surg, 123, pp.601~609 (2022)
- Kotagudda Ranganath S, "Bilateral double site(calvarial and mandibular)critical-size bone defect model in rabbits for evaluation of a craniofacial tissue engineering constructs", Mater Today Bio, 14, pp.100267~ (2022)
- Xia D, "Additively manufactured pure zinc porous scaffolds for critical-sized bone defects of rabbit femur", Bioact Mater, 19, pp.12~23 (2022)
- Zhang Z, "Stromal cell-derived factor(SDF)-1α and platelet-rich plasma enhance bone regeneration and angiogenesis simultaneously in situ in rabbit calvaria", J Mater Sci Mater Med, 32, pp.125~ (2021)
- Acar AH, "Bone regeneration by low-level laser therapy and low-intensity pulsed ultrasound therapy in the rabbit calvarium", Arch Oral Biol, 61, pp.60~65 (2016)
- Stockmann P, "Guided bone regeneration in pig calvarial bone defects using autologous mesenchymal stem", progenitor cells-a comparison of different tissue sources, 2012, pp.40, 310~320
- Eyckmans J, "Adhesive and mechanical regulation of mesenchymal stem cell differentiation in human bone marrow and periosteum-derived progenitor cells", Biol Open, 1, pp.1058~1068 (2012)
- Ferretti C, "Periosteum derived stem cells for regenerative medicine proposals : boosting current knowledge", World J Stem Cells, 6, pp.266~277 (2014)
- Duchamp de Lageneste O, "Periosteum contains skeletal stem cells with high bone regenerative potential controlled by Periostin", Nat Commun, 9, pp.773~ (2018)
- Jeyaraman M, "Osteogenic and chondrogenic potential of periosteum-derived mesenchymal stromal cells : do they hold the key to the future?", Pharmaceuticals(Basel), 14, pp.1133~ (2021)
