Elsi Ferro, Antonio Laus, Rossano Atzeni, Maria Valentini, Enrico Pieroni, Massimo Pisu
Cell populations grow, shrink, and reshuffle their composition as individual cells divide, arrest, and die. Because cell division is paced by progression through the cell cycle, cell-cycle control is the fundamental axis linking intracellular regulation to population-level dynamics. Quantitatively capturing how cell-cycle regulation affects population dynamics is thus central to understanding tissue homeostasis, tumor expansion, immune responses, and the performance of cell-based bioprocesses-from tissue engineering and regenerative applications to the manufacturing of vaccines and recombinant therapeutics. In this view, a broad spectrum of mathematical models has been proposed to describe cell population dynamics, ranging from phenomenological growth laws that treat net proliferation as a black box to structured descriptions that resolve single-cell heterogeneity and link population change to cell-cycle progression. In this review, we survey deterministic frameworks for modeling cell-cycle-informed population dynamics, highlighting how modeling choices map onto accessible experimental readouts and biomedical and biotechnological questions. In doing so, we aim to provide a theoretical roadmap for readers new to the field who seek to translate intracellular cell-cycle regulation into empirically grounded population-level models. We organize models along 2 conceptual dimensions: the representation of cell-to-cell heterogeneity through increasing levels of population structure and the level of mechanistic specification of cell division through cell-cycle regulation. In particular, we discuss practical approaches to couple cell-cycle regulation to population-level dynamics-from coarse-grained to explicit multiscale couplings-and how external perturbations enter such couplings. We conclude by outlining open challenges toward cell-cycle-aware population models that match mechanistic resolution with experimental identifiability.