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.
Original language | English (US) |
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Pages (from-to) | 253-259 |
Number of pages | 7 |
Journal | Experimental Cell Research |
Volume | 358 |
Issue number | 2 |
DOIs | |
State | Published - Sep 15 2017 |
Funding
This work was funded by NIH Grants nos. R01CA200064, R01CA165309, and R013B016983 , NSF Grant no. CBET-1240416 , and LUNgevity Foundation (2015-2016 Early Detection Award, no. 2015-04 ). The TEM word made use of the EPIC facility of Northwestern University’s NUANCE Center, which has received support from the Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF ECCS-1542205 ); the MRSEC program (NSF DMR-1121262 ) at the Materials Research Center; the International Institute for Nanotechnology (IIN) ; the Keck Foundation ; and the State of Illinois, through the IIN . Appendix A This work was funded by NIH Grants nos. R01CA200064, R01CA165309, and R013B016983, NSF Grant no. CBET-1240416, and LUNgevity Foundation (2015-2016 Early Detection Award, no. 2015-04). The TEM word made use of the EPIC facility of Northwestern University's NUANCE Center, which has received support from the Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF ECCS-1542205); the MRSEC program (NSF DMR-1121262) at the Materials Research Center; the International Institute for Nanotechnology (IIN); the Keck Foundation; and the State of Illinois, through the IIN.
Keywords
- Chromatin nanostructure
- Fixation
- Partial wave spectroscopy
ASJC Scopus subject areas
- Cell Biology