University of Twente, Tissue Regeneration Department, Drienerlolaan 5,7522 NB, Enschede, The Netherlands.
Biofabrication. 2016 Feb 27;8(1):015014. doi: 10.1088/1758-5090/8/1/015014.
Swift progress in biofabrication technologies has enabled unprecedented advances in the application of developmental biology design criteria in three-dimensional scaffolds for regenerative medicine. Considering that tissues and organs in the human body develop following specific physico-chemical gradients, in this study, we hypothesized that additive manufacturing (AM) technologies would significantly aid in the construction of 3D scaffolds encompassing such gradients. Specifically, we considered surface energy and stiffness gradients and analyzed their effect on adult bone marrow derived mesenchymal stem cell differentiation into skeletal lineages. Discrete step-wise macroscopic gradients were obtained by sequentially depositing different biodegradable biomaterials in the AM process, namely poly(lactic acid) (PLA), polycaprolactone (PCL), and poly(ethylene oxide terephthalate)/poly(butylene terephthalate) (PEOT/PBT) copolymers. At the bulk level, PEOT/PBT homogeneous scaffolds supported a higher alkaline phosphatase (ALP) activity compared to PCL, PLA, and gradient scaffolds, respectively. All homogeneous biomaterial scaffolds supported also a significantly higher amount of glycosaminoglycans (GAGs) production compared to discrete gradient scaffolds. Interestingly, the analysis of the different material compartments revealed a specific contribution of PCL, PLA, and PEOT/PBT to surface energy gradients. Whereas PEOT/PBT regions were associated to significantly higher ALP activity, PLA regions correlated with significantly higher GAG production. These results show that cell activity could be influenced by the specific spatial distribution of different biomaterial chemistries in a 3D scaffold and that engineering surface energy discrete gradients could be considered as an appealing criterion to design scaffolds for osteochondral regeneration.
生物制造技术的快速发展使得在再生医学的三维支架中应用发育生物学设计标准取得了前所未有的进展。考虑到人体组织和器官是按照特定的物理化学梯度发育的,在本研究中,我们假设增材制造(AM)技术将极大地有助于构建包含这些梯度的 3D 支架。具体来说,我们考虑了表面能和刚度梯度,并分析了它们对成体骨髓间充质干细胞向骨骼谱系分化的影响。通过在 AM 过程中顺序沉积不同的可生物降解生物材料,即聚乳酸(PLA)、聚己内酯(PCL)和聚(氧化乙烯对苯二甲酸酯)/聚(丁二酸对苯二甲酸酯)(PEOT/PBT)共聚物,获得了离散的逐步宏观梯度。在体相水平上,与 PCL、PLA 和梯度支架相比,PEOT/PBT 均聚物支架支持更高的碱性磷酸酶(ALP)活性。所有均聚物生物材料支架也支持比离散梯度支架更高的糖胺聚糖(GAG)产量。有趣的是,对不同材料区室的分析表明,PCL、PLA 和 PEOT/PBT 对表面能梯度有特定的贡献。虽然 PCL 和 PLA 区域与显著更高的 ALP 活性相关,但 PEOT/PBT 区域与显著更高的 GAG 产生相关。这些结果表明,细胞活性可能受到 3D 支架中不同生物材料化学物质的特定空间分布的影响,并且可以考虑工程表面能离散梯度作为设计用于骨软骨再生的支架的有吸引力的标准。