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DETERMINATION OF IN SITU ARTICULAR CARTILAGE PERICELLULAR MATRIX PROPERTIES VIA INVERSE BEM ANALYSIS OF CHONDRON DEFORMATION

机译:通过逆BEAM分析化合物变形的原位关节软骨围细胞基质特性的测定

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The pericellular matrix (PCM) of articular cartilage is the narrow tissue region surrounding all chondrocytes. Together, the chondrocyte and its surrounding PCM have been termed the chondron. In normal cartilage, the presence of type VI collagen is exclusive to the PCM, and the PCM is believed to play a critical role in regulating biomechanical cell-matrix interactions. Since the PCM is stiffer than the chondrocyte, it has been hypothesized to play a critical role in protecting the cell while, simultaneously, facilitating the transmission of mechanical signals to the cell. Previous studies that represent the cell, PCM and extracellular matrix (ECM) as linear biphasic materials have supported this hypothesized role for the PCM [1-4]. Previous in vitro micropipette studies of isolated chondrons [5-7] have shown that the PCM Young's modulus ranges between 25-70kPa in middle and deep zone cartilage, separating it by an order of magnitude from both the chondrocyte stiffness (~1kPa) and ECM stiffness (~1MPa). In recent years, Choi et al. [8] measured changes in the three-dimensional morphology of the chondron, in situ within the ECM, under equilibrium unconfined compression of porcine cartilage explants subjected to 10-50% compressive strain (Fig. 1). Their study employed a novel 3D confocal microscopy technique, based on immunolabeling of type VI collagen, that yielded ellipsoidal approximations of undeformed and deformed chondron shapes in the superficial, middle and deep zones of the explant. In this study, an efficient computational model, based on the boundary element method (BEM), was developed and used to estimate cartilage PCM linear elastic properties based on the data reported in Choi et al. [8] for the case of middle zone cartilage under 10% compressive strain.
机译:关节软骨的围粒体基质(PCM)是围绕所有软骨细胞的狭窄组织区域。在一起,软骨细胞及其周围的PCM已被称为软骨。在正常软骨中,VI型胶原蛋白的存在是专用于PCM的,并且PCM被认为在调节生物力学细胞 - 基质相互作用方面发挥关键作用。由于PCM比软骨细胞更硬,因此已经假设在保护电池的同时,以促进机械信号传递到电池的同时发挥关键作用。以前的研究表明作为线性双相材料的细胞,PCM和细胞外基质(ECM)支持PCM [1-4]的假设作用。之前的体外微量液体研究分离的软骨[5-7]表明,PCM杨氏模量在25-70kPa之间,在中间区域和深处的水软骨中,从软骨细胞刚度(〜1kPa)和ECM两种数量级分开刚度(〜1MPa)。近年来,Choi等人。 [8]在ECM内原位测量的硬片的三维形态的变化,在猪软骨外部植物的平衡下,受到10-50%压缩菌株的(图1)。他们的研究采用了一种基于VI型胶原蛋白的免疫标记的新型3D共聚焦显微镜技术,其在浅晶,中部区域和深层区域中产生了未变形和变形的软骨形状的椭圆近似。在本研究中,基于边界元方法(BEM)的基于边界元方法(BEM)的有效计算模型基于Choi等人的数据来估算软骨PCM线性弹性特性。 [8]对于10%压缩菌株下的中间区软骨的情况。

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