Anisotropic Shape-Memory Alginate Scaffolds Functionalized with Either Type I or Type II Collagen for Cartilage Tissue Engineering

被引:1
作者
Almeida, Henrique V. [1 ,2 ]
Sathy, Binulal N. [1 ,2 ]
Dudurych, Ivan [1 ,3 ]
Buckley, Conor T. [1 ,2 ]
O'Brien, Fergal J. [1 ,4 ,5 ,6 ]
Kelly, Daniel J. [1 ,2 ,4 ,5 ,6 ]
机构
[1] Trinity Coll Dublin, Trinity Ctr Bioengn, Trinity Biomed Sci Inst, Dublin, Ireland
[2] Trinity Coll Dublin, Sch Engn, Dept Mech & Mfg Engn, Dublin, Ireland
[3] Trinity Coll Dublin, Trinity Biomed Sci Inst, Sch Med, Dublin, Ireland
[4] Trinity Coll Dublin, Adv Mat & Bioengn Res Ctr AMBER, Dublin, Ireland
[5] Royal Coll Surgeons Ireland, Dublin, Ireland
[6] Royal Coll Surgeons Ireland, Dept Anat, Tissue Engn Res Grp, Dublin, Ireland
基金
欧洲研究理事会;
关键词
cartilage; extracellular matrix; biomimetic materials; polymeric scaffolds; meniscus; AUTOLOGOUS CHONDROCYTE IMPLANTATION; MESENCHYMAL STEM-CELLS; EXTRACELLULAR-MATRIX; ARTICULAR-CARTILAGE; STROMAL CELLS; BONE-MARROW; ADHESION; INTEGRINS; CHITOSAN; CHONDROGENESIS;
D O I
10.1089/ten.tea.2016.0055
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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.
引用
收藏
页码:55 / 68
页数:14
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