Subject(s)
Arteriosclerosis/physiopathology , Blood Vessels/physiopathology , Cyclic AMP Response Element-Binding Protein/metabolism , Muscle, Smooth, Vascular/physiopathology , Animals , Arteriosclerosis/prevention & control , Blood Vessels/metabolism , Cell Division , Cyclic AMP Response Element-Binding Protein/administration & dosage , Cyclic AMP Response Element-Binding Protein/genetics , Disease Models, Animal , Genes, Dominant , Genetic Therapy , Graft Occlusion, Vascular/prevention & control , Humans , Muscle, Smooth, Vascular/drug effects , Muscle, Smooth, Vascular/metabolismABSTRACT
Levels of Pur alpha, a protein implicated in control of both DNA replication and gene transcription, fluctuate during the cell cycle, being lowest in early S phase and highest just after mitosis. Here we have employed a new video time-lapse technique enabling us to determine the cell cycle position of each cell in an asynchronous culture at a given time and to ask whether introduction of Pur alpha protein at specific times can affect cell cycle progression. Approximately 80% of all NIH3T3 cells injected with Pur alpha were inhibited from passing through mitosis. Cells injected with Pur alpha during S or G2 phases were efficiently blocked with a 4N (G2 phase) DNA level, as determined by quantitative DNA photometry of individual cells. Of the cells injected with Pur alpha during G1 phase, 40% experienced a rapid cell death characterized by extreme cellular fragmentation. Of those G1 injected cells which remained viable, approximately equal numbers were arrested with either 2N or 4N DNA levels. Cells arrested by Pur alpha in G2 phase grew to cover a large surface area. These results link fluctuations in Pur alpha levels to aspects of cell cycle control.
