Presentation
13 March 2024 Tracking autofluorescence and morphological features of cells undergoing mitosis using open-source software
Author Affiliations +
Abstract
Metabolic features of mitosis remain poorly understood because this phase of the cell cycle is rapid and heterogeneous between cells within a dish. Label-free optical metabolic imaging (OMI) can monitor rapid changes in cell metabolism with single cell resolution using two-photon microscopy of the optical redox ratio (NAD(P)H/FAD) and NAD(P)H fluorescence lifetimes. Here, we brought together image analysis tools to quantify OMI time-courses of single cells undergoing mitosis across multiple cell lines. Alignment of OMI and morphological features over time provided unique insight into metabolic changes during mitosis within unperturbed systems.
Conference Presentation
© (2024) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Emmanuel Contreras Guzman, Rupsa Datta, Jeremiah Riendeau, Kiera M. Sapp, Matthew G. Vander Heiden, and Melissa C. Skala "Tracking autofluorescence and morphological features of cells undergoing mitosis using open-source software", Proc. SPIE PC12846, Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues XXII, PC1284605 (13 March 2024); https://doi.org/10.1117/12.3001868
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KEYWORDS
Open source software

Autofluorescence

Fluorescence

Fluorescence lifetime imaging

Imaging systems

Image segmentation

Mode conditioning cables

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