Targosz-Korecka Marta, Brzezinka Grzegorz Daniel, Danilkiewicz Joanna, Rajfur Zenon, Szymonski Marek
Research Centre for Nanometer-Scale Science and Advanced Materials, NANOSAM, Faculty of Physics, Astronomy, and Applied Computer Science, Jagiellonian University in Krakow, Krakow, Poland.
Cytoskeleton (Hoboken). 2015 Mar;72(3):124-30. doi: 10.1002/cm.21217. Epub 2015 Apr 21.
Among the users of atomic force microscopy based techniques, there is an ongoing discussion, whether cell elasticity measurements performed on fixed cells could be used for determination of the relative elasticity changes of the native (unfixed) cells subjected to physiologically active external agents. In this article, we present a case, for which the legitimacy of cell fixation for elasticity measurements is justified. We provide an evidence that the alterations of cell elasticity triggered by tumor necrosis factor alpha (TNF-α) in EA.hy926 endothelial cells are preserved after glutaraldehyde (GA) fixation. The value of post-fixation elasticity parameter is a product of the elasticity parameter obtained for living cells and a constant value, dependent on the GA concentration. The modification of the initial value of elasticity parameter caused by remodeling of the cortical actin cytoskeleton is reflected in the elasticity measurements performed on fixed cells. Thus, such fixation procedure may be particularly helpful for experiments, where the influence of an external agent on the cell cortex should be assessed and AFM measurements of living cells are problematic or better statistics is needed.
在基于原子力显微镜技术的用户中,对于在固定细胞上进行的细胞弹性测量是否可用于确定受生理活性外部因素作用的天然(未固定)细胞的相对弹性变化,一直存在讨论。在本文中,我们给出了一个案例,证明了用于弹性测量的细胞固定的合理性。我们提供了证据表明,戊二醛(GA)固定后,EA.hy926内皮细胞中由肿瘤坏死因子α(TNF-α)触发的细胞弹性变化得以保留。固定后弹性参数的值是活细胞获得的弹性参数与一个取决于GA浓度的恒定值的乘积。由皮质肌动蛋白细胞骨架重塑引起的弹性参数初始值的改变反映在对固定细胞进行的弹性测量中。因此,这种固定程序对于评估外部因素对细胞皮层的影响且活细胞的原子力显微镜测量存在问题或需要更好统计数据的实验可能特别有帮助。