An injectable hydrogel incorporating mesenchymal precursor cells and pentosan polysulphate for intervertebral disc regeneration

被引:159
作者
Frith, Jessica E. [1 ]
Cameron, Andrew R. [1 ]
Menzies, Donna J. [1 ]
Ghosh, Peter [2 ]
Whitehead, Darryl L. [3 ]
Gronthos, Stan [4 ]
Zannettino, Andrew C. W. [5 ]
Cooper-White, Justin J. [1 ,6 ,7 ]
机构
[1] Univ Queensland, Australian Inst Bioengn & Nanotechnol, St Lucia, Qld 4072, Australia
[2] Mesoblast Ltd, Melbourne, Vic 3000, Australia
[3] Univ Queensland, Sch Biomed Sci, St Lucia, Qld 4072, Australia
[4] Univ Adelaide, Fac Hlth Sci, Sch Med Sci, Mesenchymal Stem Cell Lab, Adelaide, SA 5005, Australia
[5] Univ Adelaide, Fac Hlth Sci, Sch Med Sci, Myeloma Res Lab, Adelaide, SA 5000, Australia
[6] Univ Queensland, Sch Chem Engn, St Lucia, Qld 4072, Australia
[7] CSIRO Mat Sci & Engn Div, Clayton, Vic 3168, Australia
基金
澳大利亚研究理事会;
关键词
Mesenchymal progenitor cell; Hydrogel; Nucleus pulposus; Pentosan polysulphate; Fibrocartilage; HUMAN BONE-MARROW; HYALURONIC-ACID; NUCLEUS PULPOSUS; STEM-CELLS; SYSTEM; MODULATION; GELATIN; MODULUS; SULFATE;
D O I
10.1016/j.biomaterials.2013.08.072
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Intervertebral disc (IVD) degeneration is one of the leading causes of lower back pain and a major health problem worldwide. Current surgical treatments include excision or immobilisation, with neither approach resulting in the repair of the degenerative disc. As such, a tissue engineering-based approach in which stem cells, coupled with an advanced delivery system, could overcome this deficiency and lead to a therapy that encourages functional fibrocartilage generation in the IVD. In this study, we have developed an injectable hydrogel system based on enzymatically-crosslinked polyethylene glycol and hyaluronic acid. We examined the effects of adding pentosan polysulphate (PPS), a synthetic glycosaminoglycan-like factor that has previously been shown (in vitro and in vivo) to this gel system in order to induce chondrogenesis in mesnchymal precursor cells (MPCs) when added as a soluble factor, even in the absence of additional growth factors such as TGF-beta. We show that both the gelation rate and mechanical strength of the resulting hydrogels can be tuned in order to optimise the conditions required to produce gels with the desired combination of properties for an IVD scaffold. Human immunoselected STRO-1+ MPCs were then incorporated into the hydrogels. They were shown to retain good viability after both the initial formation of the gel and for longer-term culture periods in vitro. Furthermore, MPC/hydrogel composites formed cartilage-like tissue which was significantly enhanced by the incorporation of PPS into the hydrogels, particularly with respect to the deposition of type-II-collagen. Finally, using a wild-type rat subcutaneous implantation model, we examined the extent of any immune reaction and confirmed that this matrix is well tolerated by the host. Together these data provide evidence that such a system has significant potential as both a delivery vehicle for MPCs and as a matrix for fibrocartilage tissue engineering applications. Crown Copyright (C) 2013 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:9430 / 9440
页数:11
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