Affinity-selected heparan sulfate for bone repair

被引:76
作者
Murali, S. [1 ]
Rai, B. [1 ]
Dombrowski, C. [1 ]
Lee, J. L. J. [1 ]
Lim, Z. X. H. [1 ]
Bramono, D. S. [1 ]
Ling, L. [1 ]
Bell, T. [2 ]
Hinkley, S. [2 ]
Nathan, S. S. [3 ]
Hui, J. H. [3 ]
Wong, H. K. [3 ]
Nurcombe, V. [1 ]
Cool, S. M. [1 ,3 ]
机构
[1] ASTAR, Inst Med Biol, Glycotherapeut Grp, Singapore 138648, Singapore
[2] Ind Res Ltd, Lower Hutt 5040, New Zealand
[3] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Orthopaed Surg, Singapore 119074, Singapore
关键词
Glycosaminoglycans; Heparan sulfate; Bone morphogenetic protein; Bone repair; MORPHOGENETIC PROTEIN-2; REGENERATIVE MEDICINE; CONTROLLED-RELEASE; GROWTH-FACTORS; STEM-CELLS; EXPRESSION; PROTEOGLYCANS; DIFFERENTIATION; MODEL; BMP-2;
D O I
10.1016/j.biomaterials.2013.04.017
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5594 / 5605
页数:12
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