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      Signalling, cell cycle and pluripotency in embryonic stem cells.

      Trends in Cell Biology
      Animals, Antigens, CD, physiology, Cell Cycle, Cell Differentiation, Cell Division, Cyclins, metabolism, Cytokine Receptor gp130, DNA-Binding Proteins, Embryo, Mammalian, cytology, Growth Inhibitors, Humans, Interleukin-6, Leukemia Inhibitory Factor, Lymphokines, Membrane Glycoproteins, Mice, Mitogen-Activated Protein Kinases, Models, Biological, Phosphatidylinositol 3-Kinases, Pluripotent Stem Cells, STAT3 Transcription Factor, Signal Transduction, Trans-Activators

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          Abstract

          Pluripotent mouse embryonic stem (ES) cells can be expanded in large numbers in vitro owing to a process of symmetrical self-renewal. Self-renewal entails proliferation with a concomitant suppression of differentiation. Here we describe how the cytokine leukaemia inhibitory factor (LIF) sustains self-renewal through activation of the transcription factor STAT3, and how two other signals - extracellular-signal-related kinase (ERK) and phosphatidylinositol-3-OH kinase (PI3K) - can influence differentiation and propagation, respectively. We relate these observations to the unusual cell-cycle properties of ES cells and speculate on the role of the cell cycle in maintaining pluripotency.

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