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Affinity-selected heparan sulfate for bone repair

Authors :
Saminathan S. Nathan
Bina Rai
James Hoi Po Hui
J.L.J. Lee
Diah S. Bramono
Victor Nurcombe
Hee-Kit Wong
Ling Ling
Sadasivam Murali
Simon M. Cool
Christian Dombrowski
Simon F.R. Hinkley
Zophia X.H. Lim
Tracey J. Bell
Source :
Biomaterials. 34:5594-5605
Publication Year :
2013
Publisher :
Elsevier BV, 2013.

Abstract

Bone morphogenetic protein (BMP)-2 is a potent bone healing compound produced at sites of bone trauma. Here we present a therapeutic strategy to harness the activity of endogenously produced BMP-2 by delivery of an affinity-matched heparan sulfate (HS) glycos aminoglycan biomaterial that increases the bioavailability, bioactivity and half-life of this growth factor. We have developed a robust, cost effective, peptide-based affinity platform to isolate a unique BMP-2 binding HS variant from commercially available preparations of HS, so removing the manufacturing bottleneck for their translation into the clinic. This affinity-matched HS enhanced BMP-2-induced osteogenesis through improved BMP-2 kinetics and receptor modulation, prolonged pSMAD signaling and reduced interactions with its antagonist noggin. When co-delivered with a collagen implant, the HS was as potent as exogenous BMP-2 for the healing of critical-sized bone defects in rabbits. This affinity platform can be readily tuned to isolate HS variants targeted ata range of clinically-relevant growth and adhesive factors.

Details

ISSN :
01429612
Volume :
34
Database :
OpenAIRE
Journal :
Biomaterials
Accession number :
edsair.doi.dedup.....25526eda1ef886789d680e929dee4296
Full Text :
https://doi.org/10.1016/j.biomaterials.2013.04.017