MIRA Institute for Biomedical Technology and Technical Medicine, Department of Biomaterials Science and Technology, University of Twente, Enschede, the Netherlands.
Collaborative Research Partner Annulus Fibrosus Rupture Program of AO Foundation, Davos, Switzerland.
J Tissue Eng Regen Med. 2017 Oct;11(10):2752-2762. doi: 10.1002/term.2170. Epub 2016 Jul 4.
Cell-based therapies could potentially restore the biomechanical function and enhance the self-repair capacity of annulus fibrosus (AF) tissue. However, choosing a suitable cell source and scaffold design are still key challenges. In this study, we assessed the in vitro ability of human adipose stem cells (hASCs), an easily available cell source to produce AF-like matrix in novel AF-mimetic designed scaffolds based on poly(trimethylene carbonate) and built by stereolithography. To facilitate efficient differentiation of hASCs towards AF tissue, we tested different culture medium compositions and cell seeding techniques. This is the first study to report that medium supplementation with transforming growth factor (TGF)-β3 is essential to support AF differentiation of hASCs while TGF-β1 has negligible effect after 21 days of culture. Fibrin gel seeding resulted in superior cell distribution, proliferation and AF-like matrix production of hASCs compared to direct and micromass seeding under TGF-β3 stimulation. Not only the production of sulphated glycosaminoglycans (sGAG) and collagen was significantly upregulated, but the formed collagen was also oriented and aligned into bundles within the designed pore channels. The differentiated hASCs seeded with fibrin gel were also found to have a comparable sGAG:collagen ratio and gene expression profile as native AF cells demonstrating the high potential of this strategy in AF repair. Copyright © 2016 John Wiley & Sons, Ltd.
基于聚三亚甲基碳酸酯(poly(trimethylene carbonate))的立体光刻技术构建了新型纤维环仿生支架,本研究评估了人脂肪干细胞(human adipose stem cells,hASCs)在该支架中体外产生纤维环样基质的能力。hASCs 是一种易于获得的细胞来源,为了促进 hASCs 向纤维环组织的有效分化,我们测试了不同的培养基组成和细胞接种技术。这是第一项研究报道转化生长因子-β3(transforming growth factor-β3,TGF-β3)的培养基补充对于支持 hASCs 的纤维环分化是必需的,而 TGF-β1 在培养 21 天后几乎没有影响。与 TGF-β3 刺激下的直接和微团接种相比,纤维蛋白凝胶接种导致 hASCs 具有更好的细胞分布、增殖和纤维环样基质产生。不仅硫酸化糖胺聚糖(sulphated glycosaminoglycans,sGAG)和胶原蛋白的产生显著上调,而且形成的胶原蛋白也在设计的孔道内定向排列成束。用纤维蛋白凝胶接种的分化 hASCs 的 sGAG:collagen 比值和基因表达谱也与天然纤维环细胞相当,表明该策略在纤维环修复方面具有很高的潜力。版权所有 © 2016 约翰威立父子公司