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Cellular shear adhesion force measurement and simultaneous imaging by atomic force microscope

机译:细胞剪切粘附力的测量和原子力显微镜的同时成像

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摘要

This paper presents a sensitive and fast cellular shear adhesion force measurement method using an atomic force microscope (AFM). In the work, the AFM was used both as a tool for the imaging of cells on the nano-scale and as a force sensor for the measurement of the shear adhesion force between the cell and the substrate. After the cell imaging, the measurement of cellular shear adhesion forces was made based on the different positions of the cell on the nano-scale. Moreover, different pushing speeds of probe and various locations of cells were used in experiments to study their influences. In this study, the measurement of the cell adhesion in the upper portion of the cell is different from that in the lower portion. It may reveal that the cancer cells have the metastasis tendency after cultured for 16 to 20 hours, which is significant for preventing metastasis in the patients diagnosed with early cancer lesions. Furthermore, the cellular shear adhesion forces of two types of living cancer cells were obtained based on the measurements of AFM cantilever deflections in the torsional and vertical directions. The results demonstrate that the shear adhesion force of cancer cells is twice as much as the same type of cancer cells with TRAIL. The method can also provide a way for the measurement of the cellular shear adhesion force between the cell and the substrate, and for the simultaneous exploration of cells using the AFM imaging and manipulation
机译:本文提出了一种使用原子力显微镜(AFM)的灵敏,快速的细胞剪切粘附力测量方法。在这项工作中,AFM既用作纳米级细胞成像的工具,又用作用于测量细胞与基材之间的剪切粘附力的力传感器。细胞成像后,基于细胞在纳米尺度上的不同位置进行细胞剪切粘附力的测量。此外,在实验中使用不同的探针推动速度和细胞的不同位置来研究其影响。在这项研究中,细胞上部的细胞粘附性测量与下部的细胞粘附性测量不同。这可能表明癌细胞在培养16至20小时后具有转移趋势,这对于预防诊断为早期癌症病变的患者的转移具有重要意义。此外,基于在扭转和垂直方向上的AFM悬臂挠度的测量,获得了两种类型的活癌细胞的细胞剪切粘附力。结果表明,癌细胞的剪切粘附力是使用TRAIL的相同类型癌细胞的两倍。该方法还可以提供一种测量细胞与底物之间的细胞剪切粘附力的方法,以及使用AFM成像和操作方法同时探索细胞的方法。

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