TY - JOUR
T1 - Nanoscale mineralization of cell-laden methacrylated gelatin hydrogels using calcium carbonate-calcium citrate core-shell microparticles
AU - Subbiah, Ramesh
AU - Balbinot, Gabriela De Souza
AU - Athirasala, Avathamsa
AU - Collares, Fabricio Mezzomo
AU - Sereda, Grigoriy
AU - Bertassoni, Luiz E.
N1 - Funding Information:
The authors would like to thank Anthony Tahayeri for his kind assistance for the measurement of mechanical properties. This project was supported by funding from the National Institute of Dental and Craniofacial Research (R01DE026170 and 3R01DE026170-03S1 to L. E. B.), Oregon Clinical & Translational Research Institute (OCTRI) – Biomedical Innovation Program (BIP). G. S. would like to thank Burroughs Wellcome Fund and G. S. B. would like to thank CAPES ‘‘Coordenação de Aperfeiçoamento de Pessoal de Nível Superior’’ – Brazil – Finance Code 001-Scholarship (CAPES/PRINT 88887.363280/ 2019-00).
Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2021/12/14
Y1 - 2021/12/14
N2 - Conventional biomaterials developed for bone regeneration fail to fully recapitulate the nanoscale structural organization and complex composition of the native bone microenvironment. Therefore, despite promoting osteogenic differentiation of stem cells, they fall short of providing the structural, biochemical, and mechanical stimuli necessary to drive osteogenesis for bone regeneration and function. To address this, we have recently developed a novel strategy to engineer bone-like tissue using a biomimetic approach to achieve rapid and controlled nanoscale mineralization of a cell-laden matrix in the presence of osteopontin, a non-collagenous protein, and a supersaturated solution of calcium and phosphate medium. Here, we build on this approach to engineer bone regeneration scaffolds comprising methacrylated gelatin (GelMA) hydrogels incorporated with calcium citrate core-shell microparticles as a sustained and reliable source of calcium ions for in situ mineralization. We demonstrate successful biomineralization of GelMA hydrogels by embedded calcium carbonate-calcium citrate core-shell microparticles with the resultant mineral chemistry, structure, and organization reminiscent of that of native bone. The biomimetic mineralization was further shown to promote osteogenic differentiation of encapsulated human mesenchymal stem cells even in the absence of other exogenous osteogenic induction factors. Ultimately, by combining the superior biological response engendered by biomimetic mineralization with the intrinsic tissue engineering advantages offered by GelMA, such as biocompatibility, biodegradability, and printability, we envision that our system offers great potential for bone regeneration efforts.
AB - Conventional biomaterials developed for bone regeneration fail to fully recapitulate the nanoscale structural organization and complex composition of the native bone microenvironment. Therefore, despite promoting osteogenic differentiation of stem cells, they fall short of providing the structural, biochemical, and mechanical stimuli necessary to drive osteogenesis for bone regeneration and function. To address this, we have recently developed a novel strategy to engineer bone-like tissue using a biomimetic approach to achieve rapid and controlled nanoscale mineralization of a cell-laden matrix in the presence of osteopontin, a non-collagenous protein, and a supersaturated solution of calcium and phosphate medium. Here, we build on this approach to engineer bone regeneration scaffolds comprising methacrylated gelatin (GelMA) hydrogels incorporated with calcium citrate core-shell microparticles as a sustained and reliable source of calcium ions for in situ mineralization. We demonstrate successful biomineralization of GelMA hydrogels by embedded calcium carbonate-calcium citrate core-shell microparticles with the resultant mineral chemistry, structure, and organization reminiscent of that of native bone. The biomimetic mineralization was further shown to promote osteogenic differentiation of encapsulated human mesenchymal stem cells even in the absence of other exogenous osteogenic induction factors. Ultimately, by combining the superior biological response engendered by biomimetic mineralization with the intrinsic tissue engineering advantages offered by GelMA, such as biocompatibility, biodegradability, and printability, we envision that our system offers great potential for bone regeneration efforts.
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U2 - 10.1039/d1tb01673c
DO - 10.1039/d1tb01673c
M3 - Article
C2 - 34779469
AN - SCOPUS:85120727138
SN - 2050-7518
VL - 9
SP - 9583
EP - 9593
JO - Journal of Materials Chemistry B
JF - Journal of Materials Chemistry B
IS - 46
ER -