Identification of specific cell death is of a great value for many scientists. Predominant types of cell death can be detected by flow-cytometry (FCM). Nevertheless, the absence of cellular morphology analysis leads to the misclassification of cell death type due to underestimated oncosis. However, the definition of the oncosis is important because of its potential reversibility. Therefore, FCM analysis of cell death using annexin V/propidium iodide assay was compared with holographic microscopy coupled with fluorescence detection - “Multimodal holographic microscopy (MHM)”. The aim was to highlight FCM limitations and to point out MHM advantages. It was shown that the annexin V+/PI− phenotype is not specific of early apoptotic cells, as previously believed, and that morphological criteria have to be necessarily combined with annexin V/PI for the cell death type to be ascertained precisely. MHM makes it possible to distinguish oncosis clearly from apoptosis and to stratify the progression of oncosis.

Observation and analysis of cancer cell behaviour in 3D environment is essential for full understanding of the mechanisms of cancer cell invasion. However, label-free imaging of live cells in 3D conditions is optically more challenging than in 2D. Quantitative phase imaging provided by coherence controlled holographic microscopy produces images with enhanced information compared to ordinary light microscopy and, due to inherent coherence gate effect, enables observation of live cancer cells’ activity even in scattering milieu such as the 3D collagen matrix. Exploiting the dynamic phase differences method, we for the first time describe dynamics of differences in cell mass distribution in 3D migrating mesenchymal and amoeboid cancer cells, and also demonstrate that certain features are shared by both invasion modes. We found that amoeboid fibrosarcoma cells’ membrane blebbing is enhanced upon constriction and is also occasionally present in mesenchymally invading cells around constricted nuclei. Further, we demonstrate that both leading protrusions and leading pseudopods of invading fibrosarcoma cells are defined by higher cell mass density. In addition, we directly document bundling of collagen fibres by protrusions of mesenchymal fibrosarcoma cells. Thus, such a non-invasive microscopy offers a novel insight into cellular events during 3D invasion.

Coherence-controlled holographic microscopy (CCHM) is a realtime, wide-field, and quantitative light-microscopy technique enabling 3D imaging of electromagnetic fields, providing complete information about both their intensity and phase. These attributes make CCHM a promising candidate for performance assessment of phase-altering metasurfaces, a new class of artificial materials that allow to manipulate the wavefront of passing light and thus provide unprecedented functionalities in optics and nanophotonics. In this paper, we report on our investigation of phase imaging of plasmonic metasurfaces using holographic microscopy. We demonstrate its ability to obtain phase information from the whole field of view in a single measurement on a prototypical sample consisting of silver nanodisc arrays. The experimental data were validated using FDTD simulations and a theoretical model that relates the obtained phase image to the optical response of metasurface building blocks. Finally, in order to reveal the full potential of CCHM, we employed it in the analysis of a simple metasurface represented by a plasmonic zone plate. By scanning the sample along the optical axis we were able to create a quantitative 3D phase map of fields transmitted through the zone plate. The presented results prove that CCHM is inherently suited to the task of metasurface characterization. Moreover, as the temporal resolution is limited only by the camera framerate, it can be even applied in analysis of actively tunable metasurfaces.