Moises Di Sante, Melissa Pezzotti, Julius Zimmermann, Alessandro Enrico, Joran Deschamps, Elisa Balmas, Silvia Becca, Eloisa Torchia, Giulia Ballio, Samantha Solito, Martina Sarchi, Alessandro Reali, Alessandro Bertero, Florian Jug, Francesco S Pasqualini
Cell-cycle progression is a major source of variability in live-cell phenotyping, yet imaging workflows still lack a general way to account for it alongside structural and functional readouts. Here we show CALIPERS (Cell-cycle-Aware Live-cell Imaging for Phenotyping Experiments and Regeneration Studies), an integrated framework that pairs a spectrally redesigned FUCCI reporter with continuous cell-cycle inference and flexible delivery strategies in human cells and stem-cell models. In epithelial cells, CALIPERS simultaneously images actin, tubulin, or calcium dynamics, phase-locks migration and proliferation, triggers mitosis-aware smart microscopy, and recovers fast calcium signals. In induced pluripotent stem-cell workflows, lentiviral and safe-harbor versions span pluripotent, lineage-restricted, and cardiac models. In cardiac organoids, CALIPERS tracks cell-cycle exit, tissue compaction, and calcium onset, and distinguishes productive proliferation from multinucleation and endoreplication. By making cell-cycle state an explicit, measurable variable, CALIPERS helps triage candidate regenerative interventions across diverse live-imaging assays.