Author:
Hejna Miroslav,Jorapur Aparna,Song Jun S.,Judson Robert L.
Abstract
AbstractDigital holographic microscopy permits live and label-free visualization of adherent cells. Here we report the application of this approach for high accuracy kinetic quantitative cytometry. We identify twenty-six label-free optical and morphological features that are biologically independent. When used as a basis for machine learning, these features allow blind single cell classification with up to 95% accuracy. We present methods to control for inherent holographic noise, thereby establishing a set of reliable quantitative features. Together, these contributions permit continuous digital holographic cytometry for three or more days. Applying our approach to human melanoma cells treated with a panel of cancer therapeutics, we can track the response of each cell, simultaneously classifying multiple behaviors such as cell cycle length, motility, apoptosis, senescence, and heterogeneity of response to each therapeutic. Importantly, we demonstrate relationships between these phenotypes over time. This work thus provides an experimental and computational roadmap for low cost live-cell imaging and kinetic classification of heterogeneous adherent cell populations.
Publisher
Cold Spring Harbor Laboratory
Reference45 articles.
1. Henriksen, M. , Miller, B. , Newmark, J. , Al-Kofahi, Y. & Holden, E. Recent Advances in Cytometry, Part A - Instrumentation, Methods. Methods in Cell Biology 102, (2011).
2. Taylor, D. , Haskins, J. & Giuliano, K. High content screening: A powerful approach to systems cell biology and drug discovery. Humana Press (2007).
3. A quantitative method for measuring phototoxicity of a live cell imaging microscope;Methods in enzymology,2012
4. Defining cell types and states with single-cell genomics
5. Phenotypic profiling of the human genome by time-lapse microscopy reveals cell division genes
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