Department of Bioengineering, Clemson University, Clemson, SC, USA.
Institute for Biological Interfaces of Engineering, Clemson University, Clemson, SC, USA.
Biomech Model Mechanobiol. 2018 Dec;17(6):1569-1580. doi: 10.1007/s10237-018-1044-5. Epub 2018 Jul 12.
Tendon mechanical function after injury and healing is largely determined by its underlying collagen structure, which in turn is dependent on the degree of mechanical loading experienced during healing. Experimental studies have shown seemingly conflicting outcomes: although collagen content steadily increases with increasing loads, collagen alignment peaks at an intermediate load. Herein, we explored potential collagen remodeling mechanisms that could give rise to this structural divergence in response to strain. We adapted an established agent-based model of collagen remodeling in order to simulate various strain-dependent cell and collagen interactions that govern long-term collagen content and fiber alignment. Our simulation results show two collagen remodeling mechanisms that give rise to divergent collagen content and alignment in healing tendons: (1) strain-induced collagen fiber damage in concert with increased rates of deposition at higher strains, or (2) strain-dependent rates of enzymatic degradation. These model predictions identify critical future experiments needed to isolate each mechanism's specific contribution to the structure of healing tendons.
肌腱损伤和愈合后的力学功能在很大程度上取决于其潜在的胶原结构,而胶原结构又取决于愈合过程中所经历的机械加载程度。实验研究表明,胶原含量虽然随着负荷的增加而稳步增加,但胶原排列在中等负荷时达到峰值。在此,我们探讨了可能导致这种结构差异的潜在胶原重塑机制,以响应应变。我们采用了一种已建立的基于代理的胶原重塑模型,以模拟控制长期胶原含量和纤维排列的各种与应变相关的细胞和胶原相互作用。我们的模拟结果显示了两种胶原重塑机制,它们导致愈合肌腱中的胶原含量和排列出现分歧:(1)应变诱导的胶原纤维损伤,同时在较高应变下增加沉积速率,或(2)应变依赖性的酶降解速率。这些模型预测确定了未来需要进行的关键实验,以分离每种机制对愈合肌腱结构的具体贡献。