The Influence of the Chondrocyte Microenvironment on Multiscale Articular Cartilage Mechanics: A Computational Study

IF 2.4 3区 医学 Q2 ORTHOPEDICS
Malek Adouni, Afif Gouissem, Tanvir Faisal, Yasin Y. Dhaher
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Abstract

Chondrocytes are mechanosensitive cells whose biosynthetic activity is governed by their local mechanical environment within articular cartilage. This environment is strongly influenced by the pericellular matrix (PCM), a specialized region enriched in collagen VI and a distinct non-fibrillar ground substance. However, the individual mechanical roles of these PCM constituents in regulating chondrocyte mechanotransduction remain poorly understood. In this study, an explicit, concurrent multiscale finite element model of articular cartilage was developed to directly link tissue-level loading to cellular-scale mechanics. The model incorporates anatomically realistic chondrocyte distributions, depth-dependent collagen II fibril architecture, and distinct representations of collagen VI fibrils and the non-fibrillar PCM matrix. Unconfined compression simulations were performed under reference conditions and following targeted alterations (±20%) in collagen VI stiffness, PCM matrix stiffness, or both. Results showed that tissue-level reaction forces were most sensitive to collagen VI stiffness. At the cellular scale, changes in collagen VI and PCM matrix properties significantly modulated chondrocyte circumferential forces and volumetric deformation, particularly in the superficial zone. Stress redistribution analyses revealed a load-sharing mechanism between fibrillar and non-fibrillar PCM components. These findings clarify the distinct mechanical roles of PCM constituents and provide mechanistic insight into how their degradation may disrupt chondrocyte mechanotransduction and contribute to cartilage degeneration.

软骨细胞微环境对多尺度关节软骨力学影响的计算研究。
软骨细胞是机械敏感细胞,其生物合成活性受关节软骨内局部机械环境的支配。这种环境受到细胞周围基质(PCM)的强烈影响,PCM是一个富含胶原VI和独特的非纤维性基质的特殊区域。然而,这些PCM成分在调节软骨细胞机械转导中的个体机械作用仍然知之甚少。在这项研究中,建立了一个明确的关节软骨多尺度有限元模型,将组织水平的载荷与细胞尺度力学直接联系起来。该模型结合了解剖学上真实的软骨细胞分布,深度依赖的胶原II原纤维结构,以及胶原VI原纤维和非纤维PCM基质的独特表征。在参考条件下进行无侧限压缩模拟,并对胶原VI刚度、PCM基质刚度或两者进行针对性改变(±20%)。结果表明,组织水平的反作用力对胶原VI刚度最为敏感。在细胞尺度上,胶原VI和PCM基质性质的变化显著调节了软骨细胞的周向力和体积变形,特别是在浅表区。应力重分布分析揭示了纤维和非纤维PCM组件之间的载荷分担机制。这些发现阐明了PCM成分的独特机械作用,并提供了它们的降解如何破坏软骨细胞机械转导并导致软骨退变的机制见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Orthopaedic Research®
Journal of Orthopaedic Research® 医学-整形外科
CiteScore
6.10
自引率
3.60%
发文量
261
审稿时长
3-6 weeks
期刊介绍: The Journal of Orthopaedic Research is the forum for the rapid publication of high quality reports of new information on the full spectrum of orthopaedic research, including life sciences, engineering, translational, and clinical studies.
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