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An Alternative Method to Characterize the Quasi-Static Nonlinear Material Properties of Murine Articular Cartilage

机译:表征鼠关节软骨准静态非线性物质特性的另一种方法

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摘要

With the onset and progression of osteoarthritis (OA), articular cartilage (AC) mechanical properties are altered. These alterations can serve as an objective measure of tissue degradation. Although the mouse is a common and useful animal model for studying OA, it is extremely challenging to measure the mechanical properties of murine AC due to its small size (thickness < 50 μm). In this study, we developed novel and direct approach to independently quantify two quasi-static mechanical properties of mouse AC: the load-dependent (nonlinear) solid matrix Young's modulus (E) and drained Poisson's ratio (ν). The technique involves confocal microscope-based multiaxial strain mapping of compressed, intact murine AC followed by inverse finite element analysis (iFEA) to determine E and ν. Importantly, this approach yields estimates of E and ν that are independent of the initial guesses used for iterative optimization. As a proof of concept, mechanical properties of AC on the medial femoral condyles of wild-type mice were obtained for both trypsin-treated and control specimens. After proteolytic tissue degradation induced through trypsin treatment, a dramatic decrease in E was observed (compared to controls) at each of the three tested loading conditions. A significant decrease in ν due to trypsin digestion was also detected. These data indicate that the method developed in this study may serve as a valuable tool for comparative studies evaluating factors involved in OA pathogenesis using experimentally induced mouse OA models.
机译:随着骨关节炎(OA)的发作和发展,关节软骨(AC)的机械性能发生改变。这些改变可以作为组织退化的客观指标。尽管小鼠是研究OA的常用动物模型,但由于其体积小(厚度<50μm),因此测量鼠类AC的机械性能极具挑战性。在这项研究中,我们开发了新颖且直接的方法来独立地量化鼠标AC的两个准静态机械性能:负载相关(非线性)固体基质的杨氏模量(E)和排水泊松比(ν)。该技术涉及基于共聚焦显微镜的压缩完整鼠类AC的多轴应变映射,然后进行逆有限元分析(iFEA)确定E和ν。重要的是,这种方法产生的E和ν的估计与用于迭代优化的初始猜测无关。作为概念的证明,对于胰蛋白酶处理的样品和对照样品,都获得了AC对野生型小鼠内侧股骨AC的机械性能。在通过胰蛋白酶处理诱导蛋白水解组织降解后,在三种测试的负载条件下,均观察到E的急剧下降(与对照相比)。还检测到由于胰蛋白酶消化而导致的ν显着下降。这些数据表明,本研究中开发的方法可作为比较研究中有价值的工具,使用实验诱导的小鼠OA模型评估涉及OA发病机理的因素。

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