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Evaluation of skeletal tissue repair, Part 2: Enhancement of skeletal tissue repair through dual-growth-factor-releasing hydrogels within an ex vivo chick femur defect model

Smith, E.L.; Felicity, Rose; Kanczler, J.M.; Shakesheff, Kevin; Gothard, D.; White, Lisa; Roberts, C.A.; Wells, J.A.; Qutachi, Omar; Sawkins, M.J.; Peto, H.; Rashidi, H.; Rojocd, L.; Stevens, M.M.; El Haj, A.J.; Oreffoa, R.O.C.

Authors

E.L. Smith

Profile image of FELICITY ROSE

FELICITY ROSE FELICITY.ROSE@NOTTINGHAM.AC.UK
Professor of Biomaterials and Tissue Engineering

J.M. Kanczler

Kevin Shakesheff

D. Gothard

C.A. Roberts

J.A. Wells

Omar Qutachi

M.J. Sawkins

H. Peto

H. Rashidi

L. Rojocd

M.M. Stevens

A.J. El Haj

R.O.C. Oreffoa



Abstract

There is an unmet need for improved, effective tissue engineering strategies to replace or repair bone damaged through disease or injury. Recent research has focused on developing biomaterial scaffolds capable of spatially and temporally releasing combinations of bioactive growth factors, rather than individual molecules, to recapitulate repair pathways present in vivo. We have developed an ex vivo embryonic chick femur critical size defect model and applied the model in the study of novel extracellular matrix (ECM) hydrogel scaffolds containing spatio-temporal combinatorial growth factor-releasing microparticles and skeletal stem cells for bone regeneration. Alginate/bovine bone ECM (bECM) hydrogels combined with poly(d,l-lactic-co-glycolic acid) (PDLLGA)/triblock copolymer (10–30% PDLLGA–PEG–PLDLGA) microparticles releasing dual combinations of vascular endothelial growth factor (VEGF), chondrogenic transforming growth factor beta 3 (TGF-β3) and the bone morphogenetic protein BMP2, with human adult Stro-1 + bone marrow stromal cells (HBMSCs), were placed into 2 mm central segmental defects in embryonic day 11 chick femurs and organotypically cultured. Hydrogels loaded with VEGF combinations induced host cell migration and type I collagen deposition. Combinations of TGF-β3/BMP2, particularly with Stro-1 + HBMSCs, induced significant formation of structured bone matrix, evidenced by increased Sirius red-stained matrix together with collagen expression demonstrating birefringent alignment within hydrogels. This study demonstrates the successful use of the chick femur organotypic culture system as a high-throughput test model for scaffold/cell/growth factor therapies in regenerative medicine. Temporal release of dual growth factors, combined with enriched Stro-1 + HBMSCs, improved the formation of a highly structured bone matrix compared to single release modalities. These studies highlight the potential of a unique alginate/bECM hydrogel dual growth factor release platform for bone repair.

Journal Article Type Article
Acceptance Date Apr 1, 2014
Online Publication Date Jun 4, 2014
Publication Date Oct 1, 2014
Deposit Date Sep 14, 2018
Electronic ISSN 1878-7568
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 10
Issue 10
Pages 4197-4205
DOI https://doi.org/10.1016/j.actbio.2014.05.025
Keywords Bone repair; ECM hydrogel scaffolds; Ex vivo model; Embryonic femur; Dual growth factor delivery
Public URL https://nottingham-repository.worktribe.com/output/1102009
Publisher URL https://www.sciencedirect.com/science/article/pii/S1742706114002372?via%3Dihub
PMID 00034252