Hutter J L, Chen J, Wan W K, Uniyal S, Leabu M, Chan B M C
Department of Physics & Astronomy, The University of Western Ontario, London, Canada.
J Microsc. 2005 Aug;219(Pt 2):61-8. doi: 10.1111/j.1365-2818.2005.01497.x.
Summary The atomic force microscope (AFM) has provided nanoscale analyses of surfaces of cells that exhibit strong adhesive and cell spreading properties. However, it is frequently reported that prior fixation is required for reliable imaging of cells with lower adhesive properties. In the present study, the AFM is used to assess the effects of fixation by glutaraldehyde on the elastic modulus of a human rhabdomyosarcoma transfectant cell line RDX2C2. Our results show a sharp increase in the elastic modulus for even mild fixation (0.5% glutaraldehyde for 60 s), accompanied by a dramatic improvement in imaging reproducibility. An even larger increase is seen in NIH-3T3 mouse fibroblasts, although in that case fixation is not typically necessary for successful imaging. In addition, our results suggest that treatment with glutaraldehyde restricts the content of the resulting images to features nearer to the cell surface.
摘要 原子力显微镜(AFM)已对具有强粘附和细胞铺展特性的细胞表面进行了纳米级分析。然而,经常有报道称,对于粘附性较低的细胞,需要进行预先固定才能获得可靠的成像。在本研究中,使用AFM评估戊二醛固定对人横纹肌肉瘤转染细胞系RDX2C2弹性模量的影响。我们的结果表明,即使是轻度固定(0.5%戊二醛处理60秒),弹性模量也会急剧增加,同时成像再现性也有显著改善。在NIH-3T3小鼠成纤维细胞中观察到更大的增加,尽管在这种情况下,成功成像通常不需要固定。此外,我们的结果表明,戊二醛处理会将所得图像的内容限制在更靠近细胞表面的特征上。