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Acceleration of Bone Regeneration Induced by a Soft‐Callus Mimetic Material

Clinical implementation of endochondral bone regeneration (EBR) would benefit from the engineering of devitalized cartilaginous constructs of allogeneic origins. Nevertheless, development of effective devitalization strategies that preserves extracellular matrix (ECM) is still challenging. The aim o...

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Autores principales: Longoni, Alessia, Utomo, Lizette, Robinson, Abbie, Levato, Riccardo, Rosenberg, Antoine J. W. P., Gawlitta, Debby
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8867155/
https://www.ncbi.nlm.nih.gov/pubmed/34962103
http://dx.doi.org/10.1002/advs.202103284
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author Longoni, Alessia
Utomo, Lizette
Robinson, Abbie
Levato, Riccardo
Rosenberg, Antoine J. W. P.
Gawlitta, Debby
author_facet Longoni, Alessia
Utomo, Lizette
Robinson, Abbie
Levato, Riccardo
Rosenberg, Antoine J. W. P.
Gawlitta, Debby
author_sort Longoni, Alessia
collection PubMed
description Clinical implementation of endochondral bone regeneration (EBR) would benefit from the engineering of devitalized cartilaginous constructs of allogeneic origins. Nevertheless, development of effective devitalization strategies that preserves extracellular matrix (ECM) is still challenging. The aim of this study is to investigate EBR induced by devitalized, soft callus‐mimetic spheroids. To challenge the translatability of this approach, the constructs are generated using an allogeneic cell source. Neo‐bone formation is evaluated in an immunocompetent rat model, subcutaneously and in a critical size femur defect. Living spheroids are used as controls. Also, the effect of spheroid maturation towards hypertrophy is evaluated. The devitalization procedure successfully induces cell death without affecting ECM composition or bioactivity. In vivo, a larger amount of neo‐bone formation is observed for the devitalized chondrogenic group both ectopically and orthotopically. In the femur defect, accelerated bone regeneration is observed in the devitalized chondrogenic group, where defect bridging is observed 4 weeks post‐implantation. The authors' results show, for the first time, a dramatic increase in the rate of bone formation induced by devitalized soft callus‐mimetics. These findings pave the way for the development of a new generation of allogeneic, “off‐the‐shelf” products for EBR, which are suitable for the treatment of every patient.
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spelling pubmed-88671552022-02-27 Acceleration of Bone Regeneration Induced by a Soft‐Callus Mimetic Material Longoni, Alessia Utomo, Lizette Robinson, Abbie Levato, Riccardo Rosenberg, Antoine J. W. P. Gawlitta, Debby Adv Sci (Weinh) Research Articles Clinical implementation of endochondral bone regeneration (EBR) would benefit from the engineering of devitalized cartilaginous constructs of allogeneic origins. Nevertheless, development of effective devitalization strategies that preserves extracellular matrix (ECM) is still challenging. The aim of this study is to investigate EBR induced by devitalized, soft callus‐mimetic spheroids. To challenge the translatability of this approach, the constructs are generated using an allogeneic cell source. Neo‐bone formation is evaluated in an immunocompetent rat model, subcutaneously and in a critical size femur defect. Living spheroids are used as controls. Also, the effect of spheroid maturation towards hypertrophy is evaluated. The devitalization procedure successfully induces cell death without affecting ECM composition or bioactivity. In vivo, a larger amount of neo‐bone formation is observed for the devitalized chondrogenic group both ectopically and orthotopically. In the femur defect, accelerated bone regeneration is observed in the devitalized chondrogenic group, where defect bridging is observed 4 weeks post‐implantation. The authors' results show, for the first time, a dramatic increase in the rate of bone formation induced by devitalized soft callus‐mimetics. These findings pave the way for the development of a new generation of allogeneic, “off‐the‐shelf” products for EBR, which are suitable for the treatment of every patient. John Wiley and Sons Inc. 2021-12-28 /pmc/articles/PMC8867155/ /pubmed/34962103 http://dx.doi.org/10.1002/advs.202103284 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Longoni, Alessia
Utomo, Lizette
Robinson, Abbie
Levato, Riccardo
Rosenberg, Antoine J. W. P.
Gawlitta, Debby
Acceleration of Bone Regeneration Induced by a Soft‐Callus Mimetic Material
title Acceleration of Bone Regeneration Induced by a Soft‐Callus Mimetic Material
title_full Acceleration of Bone Regeneration Induced by a Soft‐Callus Mimetic Material
title_fullStr Acceleration of Bone Regeneration Induced by a Soft‐Callus Mimetic Material
title_full_unstemmed Acceleration of Bone Regeneration Induced by a Soft‐Callus Mimetic Material
title_short Acceleration of Bone Regeneration Induced by a Soft‐Callus Mimetic Material
title_sort acceleration of bone regeneration induced by a soft‐callus mimetic material
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8867155/
https://www.ncbi.nlm.nih.gov/pubmed/34962103
http://dx.doi.org/10.1002/advs.202103284
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