Literature DB >> 28673821

The effects of chemical fixation on the cellular nanostructure.

Yue Li1, Luay M Almassalha2, John E Chandler2, Xiang Zhou2, Yolanda E Stypula-Cyrus2, Karl A Hujsak3, Eric W Roth3, Reiner Bleher3, Hariharan Subramanian2, Igal Szleifer4, Vinayak P Dravid5, Vadim Backman4.   

Abstract

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.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Chromatin nanostructure; Fixation; Partial wave spectroscopy

Mesh:

Substances:

Year:  2017        PMID: 28673821      PMCID: PMC5726765          DOI: 10.1016/j.yexcr.2017.06.022

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


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