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Big softer hole on living cells: elasticity imaging with AFM

机译:活细胞上较大的较软的孔:AFM的弹性成像

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Abstract: We have focused on effects of local mechanical properties of the cell on cell motion. By using atomic force microscopy, we measured spatial distribution of local elastic modulus on mouse fibroblasts, which is living in a physiological condition. In order to examine validity of AFM elastic measurements, we measured local elastic modulus of gels as elastic reference materials. The results obtained with AFM were compared with values obtained by tensile creep method. It is verified that these values are proportional each other. The AFM experiments on living cells revealed that center area of cell surface is about 10 times softer than the surroundings and looks like a big softer hole in the elasticity image. We fixed the cell just after the AFM measurements and carried out immunofluorescence observation for cytoskeletal filaments of actin filaments, microtubules and intermediate filaments. A comparison between distribution of local elasticity and cytoskeletones indicates that harder area on the cell results mainly from concentration of actin filaments. However, we found that some areas like the big softer hole do not correspond to distribution of actin filaments. !19
机译:摘要:我们集中研究了细胞局部机械性质对细胞运动的影响。通过使用原子力显微镜,我们测量了生活在生理条件下的小鼠成纤维细胞上局部弹性模量的空间分布。为了检验AFM弹性测量的有效性,我们测量了作为弹性参考材料的凝胶的局部弹性模量。将通过AFM获得的结果与通过拉伸蠕变法获得的值进行比较。确认这些值彼此成比例。原子力显微镜对活细胞的实验表明,细胞表面的中心区域比周围环境软了约10倍,并且在弹性图像中看起来像一个更大的软孔。我们在AFM测量后就固定了细胞,并对肌动蛋白丝,微管和中间丝的细胞骨架丝进行了免疫荧光观察。局部弹性分布和细胞骨架分布之间的比较表明,细胞上较硬的区域主要是肌动蛋白丝的集中所致。但是,我们发现某些区域(例如较大的较软的孔)并不对应于肌动蛋白丝的分布。 !19

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