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
(2022) Advanced Science, volume 9, issue 6, pp. 1 - 14
(Article)
Abstract
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
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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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Keywords: allogeneic, devitalization, endochondral bone tissue regeneration, mesenchymal stromal cells, orthotopic bone defect, General Engineering, General Physics and Astronomy, General Chemical Engineering, General Materials Science, Biochemistry, Genetics and Molecular Biology (miscellaneous), Medicine (miscellaneous), Journal Article
Publisher: Wiley-VCH Verlag
Note: Funding Information: Project no. S‐16‐130G was supported by the AO Foundation. The antibody against collagen type II (II‐II6B3), developed by T. F. Linsenmayer, was obtained from the DSHB developed under the auspices of the NICHD and maintained by The University of Iowa, Department of Biology, Iowa City, IA52242. R.L. acknowledges funding from the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programme (grant agreement No. 949806). Finally, the authors would like to thank Anja van der Sar for her gracious support during the animal experiments. Funding Information: Project no. S-16-130G was supported by the AO Foundation. The antibody against collagen type II (II-II6B3), developed by T. F. Linsenmayer, was obtained from the DSHB developed under the auspices of the NICHD and maintained by The University of Iowa, Department of Biology, Iowa City, IA52242. R.L. acknowledges funding from the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programme (grant agreement No. 949806). Finally, the authors would like to thank Anja van der Sar for her gracious support during the animal experiments. Publisher Copyright: © 2021 The Authors. Advanced Science published by Wiley-VCH GmbH
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