Li Yue, Almassalha Luay M, Chandler John E, Zhou Xiang, Stypula-Cyrus Yolanda E, Hujsak Karl A, Roth Eric W, Bleher Reiner, Subramanian Hariharan, Szleifer Igal, Dravid Vinayak P, Backman Vadim
Applied Physics Program, Northwestern University, Evanston, IL, USA.
Department of Biomedical Engineering, Northwestern University, Evanston, IL, USA.
Exp Cell Res. 2017 Sep 15;358(2):253-259. doi: 10.1016/j.yexcr.2017.06.022. Epub 2017 Jun 30.
Chemical fixation is nearly indispensable in the biological sciences, especially in circumstances where cryo-fixation is not applicable. While universally employed for the preservation of cell organization, chemical fixatives often introduce artifacts that can confound identification of true structures. Since biological research is increasingly probing ever-finer details of the cellular architecture, it is critical to understand the nanoscale transformation of the cellular organization due to fixation both systematically and quantitatively. In this work, we employed Partial Wave Spectroscopic (PWS) Microscopy, a nanoscale sensitive and label-free live cell spectroscopic-imaging technique, to analyze the effects of the fixation process through three commonly used fixation protocols for cells in vitro. In each method investigated, we detected dramatic difference in both nuclear and cytoplasmic nanoarchitecture between live and fixed states. But significantly, despite the alterations in cellular nanoscale organizations after chemical fixation, the population differences in chromatin structure (e.g. induced by a specific chemotherapeutic agent) remains. In conclusion, we demonstrated that the nanoscale cellular arrangement observed in fixed cells was fundamentally divorced from that in live cells, thus the quantitative analysis is only meaningful on the population level. This finding highlights the importance of live cell imaging techniques with nanoscale sensitivity or cryo-fixation in the interrogation of cellular structure, to complement more traditional chemical fixation methods.
化学固定在生物科学领域几乎不可或缺,尤其是在无法进行冷冻固定的情况下。虽然化学固定剂普遍用于保存细胞结构,但它们常常会引入假象,可能混淆对真实结构的识别。由于生物学研究越来越深入地探究细胞结构的细微细节,系统且定量地了解由于固定导致的细胞结构在纳米尺度上的转变至关重要。在这项工作中,我们采用了部分波谱显微镜(PWS),这是一种对纳米尺度敏感且无需标记的活细胞光谱成像技术,通过三种常用的体外细胞固定方案来分析固定过程的影响。在研究的每种方法中,我们都检测到活细胞状态和固定细胞状态在细胞核和细胞质纳米结构上存在显著差异。但重要的是,尽管化学固定后细胞的纳米尺度组织发生了改变,但染色质结构的群体差异(例如由特定化疗药物诱导的差异)仍然存在。总之,我们证明了固定细胞中观察到的纳米尺度细胞排列与活细胞中的排列根本不同,因此定量分析仅在群体水平上有意义。这一发现凸显了具有纳米尺度敏感性的活细胞成像技术或冷冻固定在研究细胞结构方面的重要性,以补充更传统的化学固定方法。