HETEROGENEITY IN THE MOUSE EPIDERMAL-CELL CYCLE ANALYZED BY COMPUTER-SIMULATIONS

Different sets of cell kinetic data obtained over many years from hairless mouse epidermis have been simulated by a mathematical model including circadian variations. Simulating several independent sets of data with the same mathematical model strengthens the validity of the results obtained. The data simulated in this investigation were all obtained with the experimental system in a state of natural synchrony. The data include cell cycle phase distributions measured by DNA flow cytometry of isolated epidermal basal cells, fractions of tritiated thymidine ([H-3]TdR) labelled cells within the cell cycle phases measured by cell sorting at intervals after [H-3]TdR pulse labelling, bivariate bromodeoxyuridine (BrdUrd)/DNA data from epidermal basal cells isolated at intervals after pulse labelling with BrdUrd, mitotic rate and per cent labelled mitosis (PLM) data from histologic sections. The following main new findings were made from the simulations: the second PLM peak observed at about 35 h after pulse labelling is hardly influenced by circadian variations; the peak is mainly determined by persisting synchrony of a rapidly cycling population with a G1-duration (T(G1)) of 20 h to 30 h; and there is a highly significant population of slowly cycling G1-cells (G1sigma). However, no significant circadian variations were found in the number of these cells.