Interferon-γ impairs physiologic downregulation of cyclin-dependent kinase inhibitor, p27 Kip1, during G1 phase progression in macrophages

Abstract

Cell cycle progression of mouse macrophage cells was impaired by interferon-gamma (IFN-γ). The blockage of G1/S transition was associated with diminution of cyclin-dependent kinase-2 (CDK2)-associated kinase activities. The expression of p21 Cip1 was not upregulated by IFN-γ. Instead, the physiologic downregulation of p27 Kip1 necessary for normal cell cycle progression did not take place sufficiently in the presence of IFN-γ. During normal cell cycle progression, the levels of p27 Kip1 were maximal at early G1 and then decreased gradually. In the presence of IFN-γ, however, the levels of p27 Kip1 discontinued to decrease at a late mid G1 point and were consistently as high as, or higher than, levels observed there. The steady, relatively high-level attachment of p27 Kip1 to CDK2 contributed to the insufficient formation of active cyclin/CDK2, possibly deferring cells from entering S phase.