EpiFlow: multidimensional single-cell epigenetic profiling by spectral flow cytometry
Jose Ruiz-IglesiasiD, Elena R. BovolentaiD, Lucía Cañizares-MoscatoiD, Javier Isoler‐AlcaráziD, Lucia Martin-RodrigueziD, Joana SeguraiD, Violeta Enriquez-ZarralangaiD, Adrian de Rus-MorenoiD, Aida Contreras-PéreziD, Alicia Gómez-MoyaiD, Dafne García-MateosiD, José Antonio TerceroiD, Bénédicte DesvoyesiD, Ana Martínez‐ValiD, Emilio CamafeitaiD, Jesús VázqueziD, Daniel Jiménez‐CarreteroiD, Berta Raposo-PonceiD, María Dolores LedesmaiD, Natalia Reglero-RealiD, Carlos PereaiD, Emilio LeconaiD, Marı́a GómeziD, Núria MartíneziD, Ernest PalomeriD
Abstract
The epigenetic landscape of individual cells determines their identity and function, yet current methods for profiling chromatin modifications at single-cell resolution remain low-throughput, costly, or limited in parametric depth. Here we present EpiFlow, a spectral flow cytometry-based platform that enables the simultaneous quantification of 16 epigenetic markers, including histone post-translational modifications, DNA methylation, and hydroxymethylation, at the single-cell level. We demonstrate that EpiFlow is robust across species from yeast to mammals and resolves biologically meaningful epigenetic transitions during the cell cycle, stem cell differentiation, germinal centre B cell maturation, diabetic liver remodelling, and seizure-induced chromatin reprogramming. High-dimensional integration of EpiFlow data enables cell-type classification based solely on epigenetic profiles in liver, brain, blood, and cancer. Furthermore, EpiFlow detects on-target and off-target/indirect effects of epigenetic drugs in a high-throughput-compatible format. Collectively, these results establish EpiFlow as a broadly applicable platform for single-cell epigenetic analysis in basic, pharmaceutical, and translational research.
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