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Biomechanics of single chondrocytes under direct shear

机译:直接剪切作用下单个软骨细胞的生物力学

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Articular chondrocytes experience a variety of mechanical stimuli during daily activity. One such stimulus, direct shear, is known to affect chondrocyte homeostasis and induce catabolic or anabolic pathways. Understanding how single chondrocytes respond biomechanically and morphologically to various levels of applied shear is an important first step toward elucidating tissue level responses and disease etiology. To this end, a novel videocapture method was developed in this study to examine the effect of direct shear on single chondrocytes, applied via the controlled lateral displacement of a shearing probe. Through this approach, precise force and deformation measurements could be obtained during the shear event, as well as clear pictures of the initial cell-to-probe contact configuration. To further study the non-uniform shear characteristics of single chondrocytes, the probe was positioned in three different placement ranges along the cell height. It was observed that the apparent shear modulus of single chondrocytes decreased as the probe transitioned from being close to the cell base (4.1 +/- 1.3 kPa), to the middle of the cell (2.6 +/- 1.1 kPa), and then near its top (1.7 +/- 0.8 kPa). In addition, cells experienced the greatest peak forward displacement (similar to 30% of their initial diameter) when the probe was placed low, near the base. Forward cell movement during shear, regardless of its magnitude, continued until it reached a plateau at similar to 35% shear strain for all probe positions, suggesting that focal adhesions become activated at this shear level to firmly adhere the cell to its substrate. Based on intracellular staining, the observed height-specific variation in cell shear stiffness and plateau in forward cell movement appeared to be due to a rearrangement of focal adhesions and actin at higher shear strains. Understanding the fundamental mechanisms at play during shear of single cells will help elucidate potential treatments for chondrocyte pathology and loading regimens related to cartilage health and disease.
机译:关节软骨细胞在日常活动中会经历各种机械刺激。已知一种这样的刺激,即直接剪切,可影响软骨细胞稳态并诱导分解代谢或合成代谢途径。了解单个软骨细胞如何对各种水平的剪切作用进行生物力学和形态学反应,是阐明组织水平反应和疾病病因的重要的第一步。为此,在这项研究中开发了一种新颖的视频捕获方法,以检查通过剪切探针的受控横向位移施加的直接剪切对单个软骨细胞的影响。通过这种方法,可以在剪切事件期间获得精确的力和变形测量值,以及初始的单元到探针接触配置的清晰图片。为了进一步研究单个软骨细胞的非均匀剪切特性,将探针沿细胞高度放置在三个不同的放置范围内。观察到,随着探针从接近细胞底部(4.1 +/- 1.3 kPa),过渡到细胞中间(2.6 +/- 1.1 kPa),然后接近,过渡时,单个软骨细胞的表观剪切模量降低。最高(1.7 +/- 0.8 kPa)。此外,当将探针放低并靠近碱基时,细胞会经历最大的峰值向前位移(近似于其初始直径的30%)。无论剪切强度如何,细胞在剪切过程中的向前运动一直持续到所有探针位置都达到类似于35%剪切应变的平稳状态,表明粘着斑在此剪切水平下被激活,从而将细胞牢固地粘附在其基底上。基于细胞内染色,观察到的细胞向前剪切运动中细胞剪切刚度和平台的高度特异性变化似乎是由于在较高剪切应变下粘着斑和肌动蛋白的重排所致。了解单细胞剪切过程中起作用的基本机制将有助于阐明软骨细胞病理学和与软骨健康和疾病相关的负荷方案的潜在治疗方法。

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