TY - JOUR
T1 - Evaluation of the osteoinductive potential of a bio-inspired scaffold mimicking the osteogenic niche for bone augmentation
AU - Minardi, Silvia
AU - Corradetti, Bruna
AU - Taraballi, Francesca
AU - Sandri, Monica
AU - Van Eps, Jeffrey
AU - Cabrera, Fernando J.
AU - Weiner, Bradley K.
AU - Tampieri, Anna
AU - Tasciotti, Ennio
N1 - Funding Information:
The authors acknowledge Dr. Jianhua Gu and HMRI SEM core, and Dr. Kemi Cui and HMRI ACTM core. Authors thank the Pre-clinical Catheterization lab of HMRI for DynaCT analysis. The authors thank Dr. Bayan Aghdasi, for providing the specimen of human trabecular bone utilized in this study. We thank Massimiliano Dapporto for the support with acquiring the XRD spectra. This study was supported by the Brown Foundation (Project ID: 18130011 ), by the Cullen Trust for Health Care Foundation (Project ID: 18130014 ) and by the EU through the grant SMILEY FP7-NMP-2012-SMALL-6-310637 (2012-15).
Publisher Copyright:
© 2015 The Authors.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2015/9/1
Y1 - 2015/9/1
N2 - Augmentation of regenerative osteogenesis represents a premier clinical need, as hundreds of thousands of patients are left with insufficient healing of bony defects related to a host of insults ranging from congenital abnormalities to traumatic injury to surgically-induced deficits. A synthetic material that closely mimics the composition and structure of the human osteogenic niche represents great potential to successfully address this high demand. In this study, a magnesium-doped hydroxyapatite/type I collagen scaffold was fabricated through a biologically-inspired mineralization process and designed to mimic human trabecular bone. The composition of the scaffold was fully characterized by XRD, FTIR, ICP and TGA, and compared to human bone. Also, the scaffold microstructure was evaluated by SEM, while its nano-structure and nano-mechanical properties were evaluated by AFM. Human bone marrow-derived mesenchymal stem cells were used to test the in vitro capability of the scaffold to promote osteogenic differentiation. The cell/scaffold constructs were cultured up to 7 days and the adhesion, organization and proliferation of the cells were evaluated. The ability of the scaffold to induce osteogenic differentiation of the cells was assessed over 3 weeks and the correlate gene expression for classic genes of osteogenesis was assessed. Finally, when tested in an ectopic model in rabbit, the scaffold produced a large volume of trabecular bone in only two weeks, that subsequently underwent maturation over time as expected, with increased mature cortical bone formation, supporting its ability to promote bone regeneration in clinically-relevant scenarios. Altogether, these results confirm a high level of structural mimicry by the scaffold to the composition and structure of human osteogenic niche that translated to faster and more efficient osteoinduction in vivo - features that suggest such a biomaterial may have great utility in future clinical applications where bone regeneration is required.
AB - Augmentation of regenerative osteogenesis represents a premier clinical need, as hundreds of thousands of patients are left with insufficient healing of bony defects related to a host of insults ranging from congenital abnormalities to traumatic injury to surgically-induced deficits. A synthetic material that closely mimics the composition and structure of the human osteogenic niche represents great potential to successfully address this high demand. In this study, a magnesium-doped hydroxyapatite/type I collagen scaffold was fabricated through a biologically-inspired mineralization process and designed to mimic human trabecular bone. The composition of the scaffold was fully characterized by XRD, FTIR, ICP and TGA, and compared to human bone. Also, the scaffold microstructure was evaluated by SEM, while its nano-structure and nano-mechanical properties were evaluated by AFM. Human bone marrow-derived mesenchymal stem cells were used to test the in vitro capability of the scaffold to promote osteogenic differentiation. The cell/scaffold constructs were cultured up to 7 days and the adhesion, organization and proliferation of the cells were evaluated. The ability of the scaffold to induce osteogenic differentiation of the cells was assessed over 3 weeks and the correlate gene expression for classic genes of osteogenesis was assessed. Finally, when tested in an ectopic model in rabbit, the scaffold produced a large volume of trabecular bone in only two weeks, that subsequently underwent maturation over time as expected, with increased mature cortical bone formation, supporting its ability to promote bone regeneration in clinically-relevant scenarios. Altogether, these results confirm a high level of structural mimicry by the scaffold to the composition and structure of human osteogenic niche that translated to faster and more efficient osteoinduction in vivo - features that suggest such a biomaterial may have great utility in future clinical applications where bone regeneration is required.
KW - Biomimetic material
KW - Biomineralization
KW - Bone regeneration
KW - Hydroxyapatite
KW - Stem cells
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U2 - 10.1016/j.biomaterials.2015.05.011
DO - 10.1016/j.biomaterials.2015.05.011
M3 - Article
C2 - 26048479
AN - SCOPUS:84930789350
SN - 0142-9612
VL - 62
SP - 128
EP - 137
JO - Biomaterials
JF - Biomaterials
ER -