Wang Yunjie, Zeinali-Davarani Shahrokh, Zhang Yanhang
Department of Mechanical Engineering, Boston University, Boston, MA 02215, USA.
Department of Mechanical Engineering, Boston University, Boston, MA 02215, USA; Department of Biomedical Engineering, Boston University, Boston, MA 02215, USA.
J Biomech. 2016 Aug 16;49(12):2358-65. doi: 10.1016/j.jbiomech.2016.02.027. Epub 2016 Feb 24.
Considering the organization and engagement behavior of different extracellular matrix (ECM) constituents in the medial and adventitial layer of the arterial wall, in this study, we proposed a new constitutive model of ECM mechanics that considers the distinct structural and mechanical contributions of medial elastin, medial collagen, and adventitial collagen, to incorporate the constituent-specific fiber orientation and the sequential fiber engagement in arterial mechanics. Planar biaxial tensile testing method was used to characterize the orthotropic and hyperelastic behavior of porcine thoracic aorta. Fiber distribution functions of medial elastin, medial collagen, and adventitial collagen were incorporated into the constitutive model. Considering the sequential engagement of ECM constituents in arterial mechanics, a recruitment density function was incorporated into the model to capture the delayed engagement of adventitial collagen. A freely jointed chain model was used to capture the mechanical behavior of elastin and collagen at the fiber level. The tissue-level ECM mechanics was obtained by incorporating fiber distribution, engagement, and elastin and collagen content. The multi-scale constitutive model considering the structural and mechanical contributions of the three major ECM constituents allows us to directly incorporate information obtained from quantitative multi-photon imaging and analysis, and biochemical assay for the prediction of tissue-level mechanical response. Moreover, the model shows promises in fitting and predicting with a small set of material parameters, which has physical meanings and can be related to the structure of the ECM.
考虑到动脉壁中层和外膜层中不同细胞外基质(ECM)成分的组织和参与行为,在本研究中,我们提出了一种新的ECM力学本构模型,该模型考虑了中层弹性蛋白、中层胶原蛋白和外膜胶原蛋白的不同结构和力学贡献,以纳入成分特异性纤维取向和动脉力学中的顺序纤维参与。采用平面双轴拉伸试验方法来表征猪胸主动脉的正交各向异性和超弹性行为。将中层弹性蛋白、中层胶原蛋白和外膜胶原蛋白的纤维分布函数纳入本构模型。考虑到ECM成分在动脉力学中的顺序参与,在模型中纳入了一个募集密度函数,以捕捉外膜胶原蛋白的延迟参与。使用自由连接链模型来捕捉弹性蛋白和胶原蛋白在纤维水平的力学行为。通过纳入纤维分布、参与以及弹性蛋白和胶原蛋白含量来获得组织水平的ECM力学。考虑到三种主要ECM成分的结构和力学贡献的多尺度本构模型使我们能够直接纳入从定量多光子成像和分析以及生化测定中获得的信息,以预测组织水平的力学响应。此外,该模型在使用一小组具有物理意义且可与ECM结构相关的材料参数进行拟合和预测方面显示出前景。