Inclusion of a 3D-printed Hyperelastic Bone mesh improves mechanical and osteogenic performance of a mineralized collagen scaffold.


Journal

Acta biomaterialia
ISSN: 1878-7568
Titre abrégé: Acta Biomater
Pays: England
ID NLM: 101233144

Informations de publication

Date de publication:
02 2021
Historique:
received: 29 08 2020
revised: 17 11 2020
accepted: 17 11 2020
pubmed: 24 11 2020
medline: 15 5 2021
entrez: 23 11 2020
Statut: ppublish

Résumé

Regenerative repair of craniomaxillofacial bone injuries is challenging due to both the large size and irregular shape of many defects. Mineralized collagen scaffolds have previously been shown to be a promising biomaterial implant to accelerate craniofacial bone regeneration in vivo. Here we describe inclusion of a 3D-printed polymer or ceramic-based mesh into a mineralized collagen scaffold to improve mechanical and biological activity. Mineralized collagen scaffolds were reinforced with 3D-printed Fluffy-PLG (ultraporous polylactide-co-glycolide co-polymer) or Hyperelastic Bone (90wt% calcium phosphate in PLG) meshes. We show degradation byproducts and acidic release from the printed structures have limited negative impact on the viability of mesenchymal stem cells. Further, inclusion of a mesh formed from Hyperelastic Bone generates a reinforced composite with significantly improved mechanical performance (elastic modulus, push-out strength). Composites formed from the mineralized collagen scaffold and either Hyperelastic Bone or Fluffy-PLG reinforcement both supported human bone-marrow derived mesenchymal stem cell osteogenesis and new bone formation. This was observed by increased mineral formation in Fluffy-PLG composites and increased cell viability and upregulation of RUNX2, Osterix, and COL1A2 genes in both composites. Strikingly, composites reinforced with Hyperelastic Bone mesh elicited significantly increased secretion of osteoprotegerin, a soluble glycoprotein and endogenous inhibitor of osteoclast activity. These results suggest that architectured meshes can be integrated into collagen scaffolds to boost mechanical performance and actively instruct cell processes that aid osteogenicity; specifically, secretion of a factor crucial to inhibiting osteoclast-mediated bone resorption. Future work will focus on further adapting the polymer mesh architecture to confer improved shape-fitting capacity as well as to investigate the role of polymer reinforcement on MSC-osteoclast interactions as a means to increase regenerative potential.

Identifiants

pubmed: 33227483
pii: S1742-7061(20)30681-4
doi: 10.1016/j.actbio.2020.11.028
pmc: PMC7856202
mid: NIHMS1650024
pii:
doi:

Substances chimiques

Collagen 9007-34-5

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

224-236

Subventions

Organisme : NIDCR NIH HHS
ID : R21 DE026582
Pays : United States

Informations de copyright

Copyright © 2020. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Marley J Dewey (MJ)

Dept. of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States.

Andrey V Nosatov (AV)

Dept. of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States.

Kiran Subedi (K)

College of Agriculture and Environmental Sciences, North Carolina Agriculture and Technical State University, Greensboro, NC 27411, United States; Dimension Inx, Chicago, IL 60616, United States. Electronic address: ksubedi@ncat.edu.

Ramille Shah (R)

Dimension Inx, Chicago, IL 60616, United States.

Adam Jakus (A)

Dimension Inx, Chicago, IL 60616, United States.

Brendan A C Harley (BAC)

Dept. of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States; Dept. of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States; Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States. Electronic address: bharley@illinois.edu.

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