Materials Science and Engineering Program, Department of Mechanical Engineering, Worcester Polytechnic Institute, Worcester, Massachusetts, USA.
Department of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, Massachusetts, USA.
J Biomed Mater Res A. 2020 Dec;108(12):2421-2434. doi: 10.1002/jbm.a.36993. Epub 2020 Jun 20.
This article presents the results of the combined effects of RGD (arginine-glycine-aspartate) functionalization and mechanical stimulation on osteogenesis that could lead to the development of implantable robust tissue-engineered mineralized constructs. Porous polycaprolactone/hydroxyapatite (PCL/HA) scaffolds are functionalized with RGD-C (arginine-glycine-aspartate-cysteine) peptide. The effects of RGD functionalization are then explored on human fetal osteoblast cell adhesion, proliferation, osteogenic differentiation (alkaline phosphatase activity), extracellular matrix (ECM) production, and mineralization over 28 days. The effects of RGD functionalization followed by mechanical stimulation with a cyclic fluid shear stress of 3.93 mPa in a perfusion bioreactor are also elucidated. The tensile properties (Young's moduli and ultimate tensile strengths) of the cell-laden scaffolds are measured at different stages of cell culture to understand how the mechanical properties of the tissue-engineered structures evolve. RGD functionalization is shown to promote initial cell adhesion, proliferation, alkaline phosphatase (ALP) activity, and ECM production. However, it does not significantly affect mineralization and tensile properties. Mechanical stimulation after RGD functionalization is shown to further improve the ALP activity, ECM production, mineralization, and tensile properties, but not cell proliferation. The results suggest that combined RGD functionalization and mechanical stimulation of cell-laden PCL/HA scaffolds can be used to accelerate the regeneration of robust bioengineered bone structures.
本文介绍了 RGD(精氨酸-甘氨酸-天冬氨酸)功能化和机械刺激对成骨的协同作用,这可能导致可植入的、坚固的组织工程矿化结构的发展。多孔聚己内酯/羟基磷灰石(PCL/HA)支架用 RGD-C(精氨酸-甘氨酸-天冬氨酸-半胱氨酸)肽进行功能化。然后研究了 RGD 功能化对人胎成骨细胞黏附、增殖、成骨分化(碱性磷酸酶活性)、细胞外基质(ECM)产生和矿化的影响,时间为 28 天。还阐明了 RGD 功能化后,在灌注生物反应器中用 3.93 mPa 的循环流体切应力进行机械刺激的效果。在细胞培养的不同阶段测量细胞负载支架的拉伸性能(杨氏模量和极限拉伸强度),以了解组织工程结构的机械性能如何演变。结果表明,RGD 功能化可促进初始细胞黏附、增殖、碱性磷酸酶(ALP)活性和 ECM 产生。然而,它对矿化和拉伸性能没有显著影响。RGD 功能化后的机械刺激进一步提高了 ALP 活性、ECM 产生、矿化和拉伸性能,但对细胞增殖没有影响。结果表明,细胞负载 PCL/HA 支架的 RGD 功能化和机械刺激的联合使用可以加速坚固的生物工程骨结构的再生。