Weldon School of Biomedical Engineering, Purdue University, 206 South Martin Jischke Drive, West Lafayette, IN 47907, United States.
Paul M. Rady Department of Mechanical Engineering, University of Colorado Boulder, 1111 Engineering Dr, Boulder, CO 80309, United States.
Acta Biomater. 2023 May;162:292-303. doi: 10.1016/j.actbio.2023.03.026. Epub 2023 Mar 24.
Fibrin is a naturally occurring protein network that forms a temporary structure to enable remodeling during wound healing. It is also a common tissue engineering scaffold because the structural properties can be controlled. However, to fully characterize the wound healing process and improve the design of regenerative scaffolds, understanding fibrin mechanics at multiple scales is necessary. Here, we present a strategy to quantify both the macroscale (1-10 mm) stress-strain response and the deformation of the mesoscale (10-1000 µm) network structure during unidirectional tensile tests. The experimental data were then used to inform a computational model to accurately capture the mechanical response of fibrin gels. Simultaneous mechanical testing and confocal microscopy imaging of fluorophore-conjugated fibrin gels revealed up to an 88% decrease in volume coupled with increase in volume fraction in deformed gels, and non-affine fiber alignment in the direction of deformation. Combination of the computational model with finite element analysis enabled us to predict the strain fields that were observed experimentally within heterogenous fibrin gels with spatial variations in material properties. These strategies can be expanded to characterize and predict the macroscale mechanics and mesoscale network organization of other heterogeneous biological tissues and matrices. STATEMENT OF SIGNIFICANCE: Fibrin is a naturally-occurring scaffold that supports cellular growth and assembly of de novo tissue and has tunable material properties. Characterization of meso- and macro-scale mechanics of fibrin gel networks can advance understanding of the wound healing process and impact future tissue engineering approaches. Using structural and mechanical characteristics of fibrin gels, a theoretical and computational model that can predict multiscale fibrin network mechanics was developed. These data and model can be used to design gels with tunable properties.
纤维蛋白是一种天然存在的蛋白质网络,它形成一个临时结构,以在伤口愈合过程中实现重塑。它也是一种常见的组织工程支架,因为其结构性能可以得到控制。然而,为了充分了解伤口愈合过程并改进再生支架的设计,有必要从多个尺度理解纤维蛋白的力学性能。在这里,我们提出了一种策略,以定量测量单向拉伸试验过程中宏观(1-10mm)的应力-应变响应和中观(10-1000μm)网络结构的变形。然后,将实验数据用于为计算模型提供信息,以准确捕捉纤维蛋白凝胶的力学响应。对荧光标记的纤维蛋白凝胶进行同步力学测试和共聚焦显微镜成像,揭示了高达 88%的体积减小,同时变形凝胶中的体积分数增加,纤维非仿射排列方向与变形方向一致。计算模型与有限元分析相结合,使我们能够预测在具有空间变化材料特性的异质纤维蛋白凝胶中观察到的实验应变场。这些策略可以扩展到表征和预测其他异质生物组织和基质的宏观力学和中观网络组织。
纤维蛋白是一种天然存在的支架,可支持细胞生长和新组织的组装,并且具有可调节的材料特性。对纤维蛋白凝胶网络的中观和宏观力学特性的描述可以促进对伤口愈合过程的理解,并影响未来的组织工程方法。利用纤维蛋白凝胶的结构和力学特性,开发了一个可以预测多尺度纤维蛋白网络力学的理论和计算模型。这些数据和模型可用于设计具有可调特性的凝胶。