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细胞外基质的完整性影响压缩状态下原位软骨细胞的力学行为。

Extracellular matrix integrity affects the mechanical behaviour of in-situ chondrocytes under compression.

机构信息

Department of Biomedical Engineering, Faculty of Engineering, University of Malaya, Kuala Lumpur, Malaysia; Human Performance Laboratory, Faculty of Kinesiology, University of Calgary, Calgary, Alberta, Canada.

Fischell Department of Bioengineering, University of Maryland, College Park, MD, United States.

出版信息

J Biomech. 2014 Mar 21;47(5):1004-13. doi: 10.1016/j.jbiomech.2014.01.003. Epub 2014 Jan 11.

Abstract

Cartilage lesions change the microenvironment of cells and may accelerate cartilage degradation through catabolic responses from chondrocytes. In this study, we investigated the effects of structural integrity of the extracellular matrix (ECM) on chondrocytes by comparing the mechanics of cells surrounded by an intact ECM with cells close to a cartilage lesion using experimental and numerical methods. Experimentally, 15% nominal compression was applied to bovine cartilage tissues using a light-transmissible compression system. Target cells in the intact ECM and near lesions were imaged by dual-photon microscopy. Changes in cell morphology (N(cell)=32 for both ECM conditions) were quantified. A two-scale (tissue level and cell level) Finite Element (FE) model was also developed. A 15% nominal compression was applied to a non-linear, biphasic tissue model with the corresponding cell level models studied at different radial locations from the centre of the sample in the transient phase and at steady state. We studied the Green-Lagrange strains in the tissue and cells. Experimental and theoretical results indicated that cells near lesions deform less axially than chondrocytes in the intact ECM at steady state. However, cells near lesions experienced large tensile strains in the principal height direction, which are likely associated with non-uniform tissue radial bulging. Previous experiments showed that tensile strains of high magnitude cause an up-regulation of digestive enzyme gene expressions. Therefore, we propose that cartilage degradation near tissue lesions may be due to the large tensile strains in the principal height direction applied to cells, thus leading to an up-regulation of catabolic factors.

摘要

软骨损伤改变了细胞的微环境,并可能通过软骨细胞的分解代谢反应加速软骨降解。在这项研究中,我们通过实验和数值方法比较了完整细胞外基质(ECM)周围的细胞和接近软骨损伤的细胞的力学性能,研究了 ECM 结构完整性对软骨细胞的影响。实验中,使用透光压缩系统对牛软骨组织施加 15%的名义压缩。通过双光子显微镜对完整 ECM 中和接近病变的靶细胞进行成像。定量研究了细胞形态的变化(两种 ECM 条件下的 N(cell)=32)。还开发了一个两尺度(组织水平和细胞水平)有限元(FE)模型。对非线性双相组织模型施加 15%的名义压缩,在瞬态和稳态下,在不同的径向位置研究相应的细胞水平模型。我们研究了组织和细胞中的格林-拉格朗日应变。实验和理论结果表明,在稳态时,接近病变的细胞的轴向变形小于完整 ECM 中的软骨细胞。然而,接近病变的细胞在主高度方向上经历了较大的拉伸应变,这可能与组织径向膨出不均匀有关。先前的实验表明,高幅度的拉伸应变会导致消化酶基因表达的上调。因此,我们提出,组织损伤附近的软骨降解可能是由于施加在细胞上的主高度方向上的大拉伸应变,从而导致分解代谢因子的上调。

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