Healing capacity of bone marrow mesenchymal stem cells versus platelet-rich fibrin in tibial bone defects of albino rats: an in vivo study [version 1; referees: 4 approved]

Background: Various techniques for tissue engineering have been introduced to aid the regeneration of defective or lost bone tissue. The aim of this study was to compare the in vivo bone-forming potential of bone marrow mesenchymal stem cells (BM-MSCs) and platelet-rich fibrin (PRF) on induced bone...

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Main Authors: Dina Rady, Rabab Mubarak, Rehab A. Abdel Moneim
Format: Article
Language:English
Published: F1000 Research Ltd 2018-09-01
Series:F1000Research
Online Access:https://f1000research.com/articles/7-1573/v1
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spelling doaj-7ce206a7271341339844c2de3417e0e62020-11-25T03:45:56ZengF1000 Research LtdF1000Research2046-14022018-09-01710.12688/f1000research.15985.117459Healing capacity of bone marrow mesenchymal stem cells versus platelet-rich fibrin in tibial bone defects of albino rats: an in vivo study [version 1; referees: 4 approved]Dina Rady0Rabab Mubarak1Rehab A. Abdel Moneim2Department of Oral Biology, Faculty of Dentistry, Cairo University, Cairo, 11553, EgyptDepartment of Oral Biology, Faculty of Dentistry, Cairo University, Cairo, 11553, EgyptDepartment of Oral Biology, Faculty of Dentistry, Cairo University, Cairo, 11553, EgyptBackground: Various techniques for tissue engineering have been introduced to aid the regeneration of defective or lost bone tissue. The aim of this study was to compare the in vivo bone-forming potential of bone marrow mesenchymal stem cells (BM-MSCs) and platelet-rich fibrin (PRF) on induced bone defects in rats’ tibiae. Methods: In total, one defect of 3-mm diameter was created in each tibia of 36 Wistar male rats. There were two groups: group A, left tibia bone defects that received PRF; and group B, right tibia bone defects of the same animal that received BM-MSCs loaded on a chitosan scaffold. Subsequently, Scanning electron microscope/energy-dispersive X-ray (SEM/EDX) analyses was performed at 3 and 10 days, and 3 weeks post‑implantation and following euthanasia; (n=12). Results: The EDX analysis performed for each group and time point revealed a significant increase in the mean calcium and phosphorous weight percentage in the BM-MSC-treated group relative to the PRF-treated group at all-time intervals (P < 0.05). Moreover, the mean calcium and phosphorus weight percentage increased as time progressed since the surgical intervention in the PRF-treated and BM-MSCs groups (P < 0.05). Conclusions: In the present study, both BM-MSCs and PRF were capable of healing osseous defects induced in a rat tibial model. Yet, BM-MSCs promoted more adequate healing, with higher mean calcium and phosphorous weight percentages than PRF at all-time points, and showed greater integration into the surrounding tissues than PRF.https://f1000research.com/articles/7-1573/v1
collection DOAJ
language English
format Article
sources DOAJ
author Dina Rady
Rabab Mubarak
Rehab A. Abdel Moneim
spellingShingle Dina Rady
Rabab Mubarak
Rehab A. Abdel Moneim
Healing capacity of bone marrow mesenchymal stem cells versus platelet-rich fibrin in tibial bone defects of albino rats: an in vivo study [version 1; referees: 4 approved]
F1000Research
author_facet Dina Rady
Rabab Mubarak
Rehab A. Abdel Moneim
author_sort Dina Rady
title Healing capacity of bone marrow mesenchymal stem cells versus platelet-rich fibrin in tibial bone defects of albino rats: an in vivo study [version 1; referees: 4 approved]
title_short Healing capacity of bone marrow mesenchymal stem cells versus platelet-rich fibrin in tibial bone defects of albino rats: an in vivo study [version 1; referees: 4 approved]
title_full Healing capacity of bone marrow mesenchymal stem cells versus platelet-rich fibrin in tibial bone defects of albino rats: an in vivo study [version 1; referees: 4 approved]
title_fullStr Healing capacity of bone marrow mesenchymal stem cells versus platelet-rich fibrin in tibial bone defects of albino rats: an in vivo study [version 1; referees: 4 approved]
title_full_unstemmed Healing capacity of bone marrow mesenchymal stem cells versus platelet-rich fibrin in tibial bone defects of albino rats: an in vivo study [version 1; referees: 4 approved]
title_sort healing capacity of bone marrow mesenchymal stem cells versus platelet-rich fibrin in tibial bone defects of albino rats: an in vivo study [version 1; referees: 4 approved]
publisher F1000 Research Ltd
series F1000Research
issn 2046-1402
publishDate 2018-09-01
description Background: Various techniques for tissue engineering have been introduced to aid the regeneration of defective or lost bone tissue. The aim of this study was to compare the in vivo bone-forming potential of bone marrow mesenchymal stem cells (BM-MSCs) and platelet-rich fibrin (PRF) on induced bone defects in rats’ tibiae. Methods: In total, one defect of 3-mm diameter was created in each tibia of 36 Wistar male rats. There were two groups: group A, left tibia bone defects that received PRF; and group B, right tibia bone defects of the same animal that received BM-MSCs loaded on a chitosan scaffold. Subsequently, Scanning electron microscope/energy-dispersive X-ray (SEM/EDX) analyses was performed at 3 and 10 days, and 3 weeks post‑implantation and following euthanasia; (n=12). Results: The EDX analysis performed for each group and time point revealed a significant increase in the mean calcium and phosphorous weight percentage in the BM-MSC-treated group relative to the PRF-treated group at all-time intervals (P < 0.05). Moreover, the mean calcium and phosphorus weight percentage increased as time progressed since the surgical intervention in the PRF-treated and BM-MSCs groups (P < 0.05). Conclusions: In the present study, both BM-MSCs and PRF were capable of healing osseous defects induced in a rat tibial model. Yet, BM-MSCs promoted more adequate healing, with higher mean calcium and phosphorous weight percentages than PRF at all-time points, and showed greater integration into the surrounding tissues than PRF.
url https://f1000research.com/articles/7-1573/v1
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