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Chondrocytes supplemented to bone graft-containing scaffolds expedite cranial defect repair

Critical maxillofacial bone fractures do not heal spontaneously, thus, often there is a need to facilitate repair via surgical intervention. Gold standard approaches, include the use of autologous bone graft, or devices supplemented with osteogenic growth factors and bone substitutes. This research...

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Autores principales: Carmon, Idan, Zobrab, Anna, Alterman, Michael, Tabib, Rami, Cohen, Adir, Kandel, Leonid, Greenberg, Alexander, Reich, Eli, Casap, Nardi, Dvir-Ginzberg, Mona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10628268/
https://www.ncbi.nlm.nih.gov/pubmed/37932515
http://dx.doi.org/10.1038/s41598-023-46604-z
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author Carmon, Idan
Zobrab, Anna
Alterman, Michael
Tabib, Rami
Cohen, Adir
Kandel, Leonid
Greenberg, Alexander
Reich, Eli
Casap, Nardi
Dvir-Ginzberg, Mona
author_facet Carmon, Idan
Zobrab, Anna
Alterman, Michael
Tabib, Rami
Cohen, Adir
Kandel, Leonid
Greenberg, Alexander
Reich, Eli
Casap, Nardi
Dvir-Ginzberg, Mona
author_sort Carmon, Idan
collection PubMed
description Critical maxillofacial bone fractures do not heal spontaneously, thus, often there is a need to facilitate repair via surgical intervention. Gold standard approaches, include the use of autologous bone graft, or devices supplemented with osteogenic growth factors and bone substitutes. This research aimed to employ a critical size calvaria defect model, to determine if the addition of chondrocytes to collagen-containing bone graft substitute, may expedite bone repair. As such, using a critical size rat calvaria defect, we implanted a collagen scaffold containing bone graft substitute (i.e., Bone graft scaffold, BG) or BG supplemented with costal chondrocytes (cBG). The rats were subjected to live CT imaging at 1, 6, 9, and 12 weeks following the surgical procedure and sacrificed for microCT imaging of the defect site. Moreover, serum markers and histological evaluation were assessed to determine osseous tissue regeneration and turnover. Live CT and microCT indicated cBG implants displayed expedited bone repair vs, BG alone, already at 6 weeks post defect induction. cBG also displayed a shorter distance between the defect edges and greater mineral apposition distance compared to BG. Summerizing, the data support the addition of chondrocytes to bone substitute, accelerates the formation of new bone within a critical size defect.
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spelling pubmed-106282682023-11-08 Chondrocytes supplemented to bone graft-containing scaffolds expedite cranial defect repair Carmon, Idan Zobrab, Anna Alterman, Michael Tabib, Rami Cohen, Adir Kandel, Leonid Greenberg, Alexander Reich, Eli Casap, Nardi Dvir-Ginzberg, Mona Sci Rep Article Critical maxillofacial bone fractures do not heal spontaneously, thus, often there is a need to facilitate repair via surgical intervention. Gold standard approaches, include the use of autologous bone graft, or devices supplemented with osteogenic growth factors and bone substitutes. This research aimed to employ a critical size calvaria defect model, to determine if the addition of chondrocytes to collagen-containing bone graft substitute, may expedite bone repair. As such, using a critical size rat calvaria defect, we implanted a collagen scaffold containing bone graft substitute (i.e., Bone graft scaffold, BG) or BG supplemented with costal chondrocytes (cBG). The rats were subjected to live CT imaging at 1, 6, 9, and 12 weeks following the surgical procedure and sacrificed for microCT imaging of the defect site. Moreover, serum markers and histological evaluation were assessed to determine osseous tissue regeneration and turnover. Live CT and microCT indicated cBG implants displayed expedited bone repair vs, BG alone, already at 6 weeks post defect induction. cBG also displayed a shorter distance between the defect edges and greater mineral apposition distance compared to BG. Summerizing, the data support the addition of chondrocytes to bone substitute, accelerates the formation of new bone within a critical size defect. Nature Publishing Group UK 2023-11-06 /pmc/articles/PMC10628268/ /pubmed/37932515 http://dx.doi.org/10.1038/s41598-023-46604-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Carmon, Idan
Zobrab, Anna
Alterman, Michael
Tabib, Rami
Cohen, Adir
Kandel, Leonid
Greenberg, Alexander
Reich, Eli
Casap, Nardi
Dvir-Ginzberg, Mona
Chondrocytes supplemented to bone graft-containing scaffolds expedite cranial defect repair
title Chondrocytes supplemented to bone graft-containing scaffolds expedite cranial defect repair
title_full Chondrocytes supplemented to bone graft-containing scaffolds expedite cranial defect repair
title_fullStr Chondrocytes supplemented to bone graft-containing scaffolds expedite cranial defect repair
title_full_unstemmed Chondrocytes supplemented to bone graft-containing scaffolds expedite cranial defect repair
title_short Chondrocytes supplemented to bone graft-containing scaffolds expedite cranial defect repair
title_sort chondrocytes supplemented to bone graft-containing scaffolds expedite cranial defect repair
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10628268/
https://www.ncbi.nlm.nih.gov/pubmed/37932515
http://dx.doi.org/10.1038/s41598-023-46604-z
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