Emmanuel Contreras Guzman,1 Rupsa Dattahttps://orcid.org/0000-0002-6432-2389,1 Jeremiah Riendeau,1 Kiera M. Sapp,2 Matthew G. Vander Heiden,2 Melissa C. Skala3,1
1Morgridge Institute for Research (United States) 2Massachusetts Institute of Technology (United States) 3Univ. of Wisconsin-Madison (United States)
PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.
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.
PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.
The alert did not successfully save. Please try again later.
Emmanuel Contreras Guzman, Rupsa Datta, Jeremiah Riendeau, Kiera M. Sapp, Matthew G. Vander Heiden, 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