Almeida Henrique V, Sathy Binulal N, Dudurych Ivan, Buckley Conor T, O'Brien Fergal J, Kelly Daniel J
1 Trinity Centre for Bioengineering, Trinity Biomedical Sciences Institute , Trinity College Dublin, Dublin, Ireland .
2 Department of Mechanical and Manufacturing Engineering, School of Engineering, Trinity College Dublin , Dublin, Ireland .
Tissue Eng Part A. 2017 Jan;23(1-2):55-68. doi: 10.1089/ten.TEA.2016.0055. Epub 2016 Nov 22.
Regenerating articular cartilage and fibrocartilaginous tissue such as the meniscus is still a challenge in orthopedic medicine. While a range of different scaffolds have been developed for joint repair, none have facilitated the development of a tissue that mimics the complexity of soft tissues such as articular cartilage. Furthermore, many of these scaffolds are not designed to function in mechanically challenging joint environments. The overall goal of this study was to develop a porous, biomimetic, shape-memory alginate scaffold for directing cartilage regeneration. To this end, a scaffold was designed with architectural cues to guide cellular and neo-tissue alignment, which was additionally functionalized with a range of extracellular matrix cues to direct stem cell differentiation toward the chondrogenic lineage. Shape-memory properties were introduced by covalent cross-linking alginate using carbodiimide chemistry, while the architecture of the scaffold was modified using a directional freezing technique. Introducing such an aligned pore structure was found to improve the mechanical properties of the scaffold, and promoted higher levels of sulfated glycosaminoglycans (sGAG) and collagen deposition compared to an isotropic (nonaligned) pore geometry when seeded with adult human stem cells. Functionalization with collagen improved stem cell recruitment into the scaffold and facilitated more homogenous cartilage tissue deposition throughout the construct. Incorporating type II collagen into the scaffolds led to greater cell proliferation, higher sGAG and collagen accumulation, and the development of a stiffer tissue compared to scaffolds functionalized with type I collagen. The results of this study demonstrate how both scaffold architecture and composition can be tailored in a shape-memory alginate scaffold to direct stem cell differentiation and support the development of complex cartilaginous tissues.
在矫形医学中,再生关节软骨和纤维软骨组织(如半月板)仍然是一项挑战。虽然已经开发出一系列不同的支架用于关节修复,但没有一种能够促进形成模仿关节软骨等软组织复杂性的组织。此外,这些支架中的许多并非设计用于在机械挑战性的关节环境中发挥作用。本研究的总体目标是开发一种多孔、仿生、形状记忆藻酸盐支架,用于引导软骨再生。为此,设计了一种具有结构线索的支架,以引导细胞和新组织排列,并用一系列细胞外基质线索进行功能化,以引导干细胞向软骨形成谱系分化。通过使用碳二亚胺化学方法对藻酸盐进行共价交联引入形状记忆特性,同时使用定向冷冻技术修改支架结构。发现引入这种排列的孔结构可改善支架的机械性能,并且与接种成人干细胞时的各向同性(未排列)孔几何形状相比,可促进更高水平的硫酸化糖胺聚糖(sGAG)和胶原蛋白沉积。用胶原蛋白进行功能化可改善干细胞向支架内的募集,并促进在整个构建体中更均匀的软骨组织沉积。与用I型胶原蛋白功能化的支架相比,将II型胶原蛋白掺入支架中可导致更大的细胞增殖、更高的sGAG和胶原蛋白积累,以及形成更硬的组织。本研究结果表明,如何在形状记忆藻酸盐支架中调整支架结构和组成,以引导干细胞分化并支持复杂软骨组织的发育。