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Autogenous bone particles combined with platelet-rich plasma can stimulate bone regeneration in rabbits

Long-term bone defects are a key clinical problem. Autogenous bone graft remains the gold standard for the treatment of these defects; however, improving the osteogenic properties and reducing the amount of autogenous bone is challenging. Autologous platelet-rich plasma (PRP) has been widely conside...

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Autores principales: Xie, Huanxin, Cao, Lei, Ye, Linlin, Du, Jubao, Shan, Guixiang, Hu, Jie, Jiang, Chunjing, Song, Weiqun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7664605/
https://www.ncbi.nlm.nih.gov/pubmed/33200004
http://dx.doi.org/10.3892/etm.2020.9409
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author Xie, Huanxin
Cao, Lei
Ye, Linlin
Du, Jubao
Shan, Guixiang
Hu, Jie
Jiang, Chunjing
Song, Weiqun
author_facet Xie, Huanxin
Cao, Lei
Ye, Linlin
Du, Jubao
Shan, Guixiang
Hu, Jie
Jiang, Chunjing
Song, Weiqun
author_sort Xie, Huanxin
collection PubMed
description Long-term bone defects are a key clinical problem. Autogenous bone graft remains the gold standard for the treatment of these defects; however, improving the osteogenic properties and reducing the amount of autogenous bone is challenging. Autologous platelet-rich plasma (PRP) has been widely considered for treatment, due to its potentially beneficial effect on bone regeneration and vascularization. The aim of the present study was to explore the effects of autogenous bone particles combined with PRP on repairing segmental bone defects in rabbits. Briefly, a critical-size diaphyseal radius defect was established in 45 New Zealand White rabbits. Animals were randomly divided into four groups, according to the different implants: Group A, empty bone defect; group B, PRP; group C, autogenous bone particles + bone mesenchymal stem cells (BMSCs) on the left radius; group D, autogenous bone particles + PRP + BMSCs on the right radius. Bone samples were collected and further analyzed using X-ray, histology and histomorphometry 4, 8 and 12 weeks post-surgery. In addition, the effect of PRP on cell proliferation was detected by Cell Counting Kit-8 and the concentrations of growth factors (GFs), transforming GF (TGF)-β1 and platelet-derived GF (PDGF), in PRP were verified by ELISA. X-ray, histology and histomorphometry data revealed that the fraction area of the newly formed bone was larger in group D. In addition, PRP could improve cell proliferation, osteogenic differentiation and the release of GFs, TGF-β1 and PDGF-AB. In conclusion, these findings indicated that an autogenous bone particle + PRP + BMSC scaffold may be used as a potential treatment strategy for segmental defects in humans.
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spelling pubmed-76646052020-11-15 Autogenous bone particles combined with platelet-rich plasma can stimulate bone regeneration in rabbits Xie, Huanxin Cao, Lei Ye, Linlin Du, Jubao Shan, Guixiang Hu, Jie Jiang, Chunjing Song, Weiqun Exp Ther Med Articles Long-term bone defects are a key clinical problem. Autogenous bone graft remains the gold standard for the treatment of these defects; however, improving the osteogenic properties and reducing the amount of autogenous bone is challenging. Autologous platelet-rich plasma (PRP) has been widely considered for treatment, due to its potentially beneficial effect on bone regeneration and vascularization. The aim of the present study was to explore the effects of autogenous bone particles combined with PRP on repairing segmental bone defects in rabbits. Briefly, a critical-size diaphyseal radius defect was established in 45 New Zealand White rabbits. Animals were randomly divided into four groups, according to the different implants: Group A, empty bone defect; group B, PRP; group C, autogenous bone particles + bone mesenchymal stem cells (BMSCs) on the left radius; group D, autogenous bone particles + PRP + BMSCs on the right radius. Bone samples were collected and further analyzed using X-ray, histology and histomorphometry 4, 8 and 12 weeks post-surgery. In addition, the effect of PRP on cell proliferation was detected by Cell Counting Kit-8 and the concentrations of growth factors (GFs), transforming GF (TGF)-β1 and platelet-derived GF (PDGF), in PRP were verified by ELISA. X-ray, histology and histomorphometry data revealed that the fraction area of the newly formed bone was larger in group D. In addition, PRP could improve cell proliferation, osteogenic differentiation and the release of GFs, TGF-β1 and PDGF-AB. In conclusion, these findings indicated that an autogenous bone particle + PRP + BMSC scaffold may be used as a potential treatment strategy for segmental defects in humans. D.A. Spandidos 2020-12 2020-10-27 /pmc/articles/PMC7664605/ /pubmed/33200004 http://dx.doi.org/10.3892/etm.2020.9409 Text en Copyright: © Xie et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Xie, Huanxin
Cao, Lei
Ye, Linlin
Du, Jubao
Shan, Guixiang
Hu, Jie
Jiang, Chunjing
Song, Weiqun
Autogenous bone particles combined with platelet-rich plasma can stimulate bone regeneration in rabbits
title Autogenous bone particles combined with platelet-rich plasma can stimulate bone regeneration in rabbits
title_full Autogenous bone particles combined with platelet-rich plasma can stimulate bone regeneration in rabbits
title_fullStr Autogenous bone particles combined with platelet-rich plasma can stimulate bone regeneration in rabbits
title_full_unstemmed Autogenous bone particles combined with platelet-rich plasma can stimulate bone regeneration in rabbits
title_short Autogenous bone particles combined with platelet-rich plasma can stimulate bone regeneration in rabbits
title_sort autogenous bone particles combined with platelet-rich plasma can stimulate bone regeneration in rabbits
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7664605/
https://www.ncbi.nlm.nih.gov/pubmed/33200004
http://dx.doi.org/10.3892/etm.2020.9409
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