Camarero-Espinosa S, Tomasina C, Calore A, Moroni L
MERLN Institute for Technology-inspired Regenerative Medicine, Complex Tissue Regeneration Department, Maastricht University, P.O. Box 616, 6200MD, Maastricht, the Netherlands.
Polyganics, Rozenburglaan 15A, 9727 DL, Groningen, the Netherlands.
Mater Today Bio. 2020 Apr 13;6:100051. doi: 10.1016/j.mtbio.2020.100051. eCollection 2020 Mar.
Articular cartilage was thought to be one of the first tissues to be successfully engineered. Despite the avascular and non-innervated nature of the tissue, the cells within articular cartilage - chondrocytes - account for a complex phenotype that is difficult to be maintained in vitro. The use of bone marrow-derived stromal cells (BMSCs) has emerged as a potential solution to this issue. Differentiation of BMSCs toward stable and non-hypertrophic chondrogenic phenotypes has also proved to be challenging. Moreover, hyaline cartilage presents a set of mechanical properties - relatively high Young's modulus, elasticity, and resilience - that are difficult to reproduce. Here, we report on the use of additive manufactured biodegradable poly(ester)urethane (PEU) scaffolds of two different structures (500 μm pore size and 90° or 60° deposition angle) that can support the loads applied onto the knee while being highly resilient, with a permanent deformation lower than 1% after 10 compression-relaxation cycles. Moreover, these scaffolds appear to promote BMSC differentiation, as shown by the deposition of glycosaminoglycans and collagens (in particular collagen II). At gene level, BMSCs showed an upregulation of chondrogenic markers, such as collagen II and the Sox trio, to higher or similar levels than that of traditional pellet cultures, with a collagen II/collagen I relative expression of 2-3, depending on the structure of the scaffold. Moreover, scaffolds with different pore architectures influenced the differentiation process and the final BMSC phenotype. These data suggest that additive manufactured PEU scaffolds could be good candidates for cartilage tissue regeneration in combination with microfracture interventions.
关节软骨曾被认为是最早成功实现组织工程化的组织之一。尽管该组织无血管且无神经支配,但其内部的细胞——软骨细胞——具有复杂的表型,难以在体外维持。骨髓来源的基质细胞(BMSC)的应用已成为解决这一问题的潜在方案。将BMSC分化为稳定且非肥大的软骨生成表型也被证明具有挑战性。此外,透明软骨具有一系列机械性能——相对较高的杨氏模量、弹性和韧性——难以复制。在此,我们报告了使用两种不同结构(孔径500μm,沉积角度为90°或60°)的增材制造可生物降解聚(酯)聚氨酯(PEU)支架,这些支架在高度有弹性的同时能够支撑施加在膝盖上的负荷,在10次压缩 - 松弛循环后永久变形低于1%。此外,这些支架似乎能促进BMSC分化,糖胺聚糖和胶原蛋白(特别是胶原蛋白II)的沉积就表明了这一点。在基因水平上,BMSC显示出软骨生成标志物(如胶原蛋白II和Sox三联体)的上调,其水平高于或类似于传统微团培养,胶原蛋白II/胶原蛋白I的相对表达为2 - 3,这取决于支架的结构。此外,具有不同孔隙结构的支架影响了分化过程和最终的BMSC表型。这些数据表明,增材制造的PEU支架结合微骨折干预可能是软骨组织再生的良好候选材料。