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Quantification of Polymer Depletion Induced Red Blood Cell Adhesion to Artificial Surfaces

机译:聚合物耗尽的定量诱导人工表面的红细胞粘附

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Cell-cell interactions are governed by interplay of various cell-receptor-mediated interactions and non-specific forces, with non-specific forces such as electrostatic repulsion often allowing or preventing cells approaching close enough to establish adhesion via lock and key forces. One non-specific force that has only recently been suggested as being important for cell-cell interaction is macromolecular depletion interaction. Polymer depletion occurs at cell surfaces if adsorption energy is low, and if depletion zones of adjacent surfaces overlap; osmotic forces move fluid away from the intercellular gap and cell-cell attractive forces develop. In this study interference reflection microscopy (IRM) was employed to study red blood cell (RBC) adhesion to glass surfaces in the presence of dextran in order to elucidate and quantify the underlying mechanism. Our results indicate that adhesion is markedly increased in the presence of dextrans with a molecular weight above 70 kDa. The calculated adhesion energies varied between 0.1 and 1 μJ/m2 and the bell-shaped relation between adhesion energy and both polymer molecular mass and concentration was in qualitative and quantitative agreement with a theoretical depletion model. A strong suppression of membrane undulations was also observed. In overview, our results indicate that depletion interaction plays a significant role in RBC adhesion via initiating close contacts. The results suggest the importance of depletion forces for RBC interactions and its relevance to a wide variety of cell-cell and cell-surface interactions.
机译:细胞 - 细胞相互作用通过各种细胞受体介导的相互作用和非特征的相互作用来控制,具有非特异性的力,例如静电排斥力通常允许或防止接近足够接近的细胞以通过锁和关键力建立粘附。唯一唯一建议对细胞 - 细胞相互作用重要的一种非特异性力是大分子耗尽相互作用。如果吸附能量低,则在细胞表面发生聚合物耗尽,如果相邻表面的耗尽区重叠;渗透力使流体远离细胞间隙和细胞 - 细胞吸引力的力。在该研究中,使用干扰反射显微镜(IRM)在葡聚糖存在下研究红细胞(RBC)对玻璃表面的粘附性,以阐明和量化下面的机制。我们的结果表明,在70kDa以上的分子量的葡聚糖存在下,粘附性显着增加。计算出的粘合能量在0.1至1μJ/ m 2之间变化,粘合能量与聚合物分子量和浓度之间的钟形关系与理论耗尽模型进行定性和定量协议。还观察到强烈抑制膜起伏。在概述中,我们的结果表明耗尽相互作用通过启动密切触点在RBC粘附中起着重要作用。结果表明RBC相互作用的耗尽力及其与各种细胞细胞和细胞表面相互作用的相关性的重要性。

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