Szczesny Spencer E, Driscoll Tristan P, Tseng Hsiao-Yun, Liu Pang-Ching, Heo Su-Jin, Mauck Robert L, Chao Pen-Hsiu G
McKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, Perelman School of Medicine, Philadelphia, Pennsylvania 19104, United States.
Department of Bioengineering, University of Pennsylvania, Philadelphia, Pennsylvania 19104, United States.
ACS Biomater Sci Eng. 2017 Nov 13;3(11):2869-2876. doi: 10.1021/acsbiomaterials.6b00646. Epub 2016 Dec 8.
To fully recapitulate tissue microstructure and mechanics, fiber crimping must exist within biomaterials used for tendon/ligament engineering. Existing crimped nanofibrous scaffolds produced via electrospinning are dense materials that prevent cellular infiltration into the scaffold interior. In this study, we used a sacrificial fiber population to increase the scaffold porosity and evaluated the effect on fiber crimping. We found that increasing scaffold porosity increased fiber crimping and ensured that the fibers properly uncrimped as the scaffolds were stretched by minimizing fiber-fiber interactions. Constitutive modeling demonstrated that the fiber uncrimping produced a nonlinear mechanical behavior similar to that of native tendon and ligament. Interestingly, fiber crimping altered strain transmission to the nuclei of cells seeded on the scaffolds, which may account for previously observed changes in gene expression. These crimped biomaterials are useful for developing functional fiber-reinforced tissues and for studying the effects of altered fiber crimping due to damage or degeneration.
为了全面重现组织微观结构和力学性能,用于肌腱/韧带工程的生物材料中必须存在纤维卷曲。通过静电纺丝制备的现有卷曲纳米纤维支架是致密材料,会阻止细胞渗入支架内部。在本研究中,我们使用了牺牲纤维群体来增加支架孔隙率,并评估其对纤维卷曲的影响。我们发现,增加支架孔隙率会增加纤维卷曲,并通过最小化纤维-纤维相互作用确保在支架拉伸时纤维能正确展开。本构模型表明,纤维展开产生了类似于天然肌腱和韧带的非线性力学行为。有趣的是,纤维卷曲改变了传递到接种在支架上细胞细胞核的应变,这可能解释了先前观察到的基因表达变化。这些卷曲生物材料可用于开发功能性纤维增强组织,以及研究因损伤或退变导致的纤维卷曲改变的影响。