Komala Ivan, Chen Yu-Ting, Chen Ying-Chun, Yeh Chih-Ching, Lu Tung-Wu
Department of Biomedical Engineering, National Taiwan University, Taiwan, ROC; Department of Aerospace Structure & Materials, Delft University of Technology, the Netherlands.
Department of Biomedical Engineering, National Taiwan University, Taiwan, ROC.
J Mech Behav Biomed Mater. 2025 Oct;170:107100. doi: 10.1016/j.jmbbm.2025.107100. Epub 2025 Jun 14.
Collagen, the most abundant protein in the human body, plays a pivotal role in the functioning of tissues such as cartilage of synovial joints. Mathematical modeling enables the more detailed study of the physical behavior of the network under load bearing. In this study, we aimed to develop a microscopic finite element (FE) modeling approach for the study of the stresses and strains of the collagen fibrils of cartilage under mechanical loading. This new approach enabled the two-dimensional modeling of a series of collagen meshwork at the microscopic level based on typical superficial collagen fibril structures of the articular cartilage. A collagen fibril network, a microscopic structure composed of 24 collagen fibrils, was designed to mimic the typical configuration found in the surface layer of cartilage. Twenty networks were developed, each representing one of three distinct crosslink density levels: high, medium, and low. This setup enabled us to investigate the effects of varying fibril connectivity on the network's morphology and its stress and strain responses under continuous biaxial tensile forces and cyclic loading, simulating the contact forces experienced by knee cartilage during walking. It was found that highly-crosslinked meshwork had greater stiffness than lower-crosslinked meshwork but with higher fibril strain under constant load, and that both the collagen meshwork and individual fibrils became stiffer with reduced deformation after several cycles. The current FE modeling approach provides new insights into the structure-function relationships of the collagen-like meshwork, with a specific focus on the unique role of fibril connectivity under mechanical loads. The current results suggest that collagen stiffening after several cyclic loading may lead to the embrittlement of collagen fibrils, altering the mechanical behavior of the cartilage. This study provides further evidence of the importance of the interfibrillar morphology of collagen meshwork in the mechanical behavior of cartilage. The current model illustrates the functional behavior of the collagen network and can be integrated into more comprehensive multiscale cartilage models that include additional components such as water and proteoglycans, thereby enabling a more complete representation of cartilage mechanics. Future research may utilize this collagen-centric model within broader, multi-phase frameworks to examine interactions between the collagen structure, fluids, and the proteoglycan network. These insights into fibril crosslink density-dependent mechanics may help elucidate early micro-mechanical changes occurring during osteoarthritis progression.
胶原蛋白是人体中含量最丰富的蛋白质,在诸如滑膜关节软骨等组织的功能发挥中起着关键作用。数学建模能够更详细地研究网络在承受负荷时的物理行为。在本研究中,我们旨在开发一种微观有限元(FE)建模方法,用于研究机械加载下软骨胶原纤维的应力和应变。这种新方法能够基于关节软骨典型的表层胶原纤维结构,在微观层面上对一系列胶原网络进行二维建模。设计了一种由24根胶原纤维组成的微观结构——胶原纤维网络,以模拟在软骨表层发现的典型构型。构建了20个网络,每个网络代表三种不同交联密度水平之一:高、中、低。这种设置使我们能够研究不同的纤维连接性对网络形态及其在连续双轴拉伸力和循环加载下的应力和应变响应的影响,模拟行走过程中膝关节软骨所承受的接触力。研究发现,高度交联的网络比低度交联的网络具有更大的刚度,但在恒定负荷下纤维应变更高,并且经过几个循环后,胶原网络和单个纤维在变形减小时都会变得更硬。当前的有限元建模方法为类胶原网络的结构 - 功能关系提供了新的见解,特别关注了机械负荷下纤维连接性的独特作用。当前结果表明,经过几次循环加载后胶原蛋白变硬可能会导致胶原纤维变脆,从而改变软骨的力学行为。本研究进一步证明了胶原网络的纤维间形态在软骨力学行为中的重要性。当前模型阐明了胶原网络的功能行为,并且可以集成到更全面的多尺度软骨模型中,这些模型包括水和蛋白聚糖等其他成分,从而能够更完整地呈现软骨力学。未来的研究可以在更广泛的多相框架内利用这个以胶原为中心的模型,来研究胶原结构、流体和蛋白聚糖网络之间的相互作用。这些对纤维交联密度依赖性力学的见解可能有助于阐明骨关节炎进展过程中早期发生的微观力学变化。