Department of Micro-Nano Systems Engineering, Nagoya University, Nagoya, Japan.
IEEE Trans Nanobioscience. 2011 Dec;10(4):217-24. doi: 10.1109/TNB.2011.2177099. Epub 2012 Jan 9.
Cell-surface adhesion force is important for cell activities and the development of bio materials. In this paper, a method for in situ single cell (W303) adhesion force measurement was proposed based on nanorobotic manipulation system inside an environment scanning electron microscope (ESEM). An end effector was fabricated from a commercial atomic force microscope (AFM) cantilever by focused ion beam (FIB) etching. The spring constant of it was calibrated by nanomanipulation approach. Three kinds of hydrophilic and hydrophobic ITO plates were prepared by using VUV-irradiation and OTS coating techniques. The shear adhesion strength of the single yeast cell to each substrate was measured based on the deflection of the end effector. The results demonstrated that the cell adhesion force was larger under the wet condition in the ESEM environment than in the aqueous condition. It also showed that the cell adhesion force to hydrophilic surface was larger than that to the hydrophobic surface. Studies of single cell's adhesion on various plate surfaces and environments could give new insights into the tissue engineering and biological field.
细胞表面黏附力对于细胞活动和生物材料的发展非常重要。本文提出了一种基于环境扫描电子显微镜(ESEM)内纳米机器人操作系统的原位单细胞(W303)黏附力测量方法。通过聚焦离子束(FIB)刻蚀,从商用原子力显微镜(AFM)悬臂梁上制造出末端执行器。通过纳米操作方法对其进行了弹性常数校准。采用 VUV 照射和 OTS 涂覆技术制备了三种亲水和疏水 ITO 板。基于末端执行器的挠度,测量了单个酵母细胞对各基底的剪切黏附强度。结果表明,ESEM 环境下的湿条件比水相中的细胞黏附力更大。还表明,细胞对亲水表面的黏附力大于对疏水表面的黏附力。对各种基底表面和环境中单细胞黏附的研究可以为组织工程和生物学领域提供新的见解。