Distinct Developmental Roles of Cell Cycle Inhibitors p57 Kip2 and p27 Kip1 Distinguish Pituitary Progenitor Cell Cycle Exit from Cell Cycle Reentry of Differentiated Cells

Abstract

ABSTRACT Patterning and differentiation signals are often believed to drive the developmental program, including cell cycle exit of proliferating progenitors. Taking advantage of the spatial and temporal separation of proliferating and differentiated cells within the developing anterior pituitary gland, we investigated the control of cell proliferation during organogenesis. Thus, we identified a population of noncycling precursors that are uniquely marked by expression of the cell cycle inhibitor p57 Kip2 and by cyclin E. In p57 Kip2−/− mice, the developing pituitary is hyperplastic due to accumulation of proliferating progenitors, whereas overexpression of p57 Kip2 leads to hypoplasia. p57 Kip2 -dependent cell cycle exit is not required for differentiation, and conversely, blockade of cell differentiation, as achieved in Tpit −/− pituitaries, does not prevent cell cycle exit but rather leads to accumulation of p57 Kip2 -positive precursors. Upon differentiation, p57 Kip2 is replaced by p27 Kip1 . Accordingly, proliferating differentiated cells are readily detected in p27 Kip1−/− pituitaries but not in wild-type or p57 Kip2−/− pituitaries. Strikingly, all cells of p57 Kip2−/− ;p27 Kip1−/− pituitaries are proliferative. Thus, during normal development, progenitor cell cycle exit is controlled by p57 Kip2 followed by p27 Kip1 in differentiated cells; these sequential actions, taken together with different pituitary outcomes of their loss of function, suggest hierarchical controls of the cell cycle that are independent of differentiation.