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      TIMP-1 stimulates proliferation of human aortic smooth muscle cells and Ras effector pathways.

      Biochemical and Biophysical Research Communications
      Animals, Aorta, anatomy & histology, Cell Line, Cell Proliferation, drug effects, Chromones, pharmacology, Cyclin D1, metabolism, Dipeptides, Enzyme Activation, Extracellular Signal-Regulated MAP Kinases, Humans, Morpholines, Myocytes, Smooth Muscle, cytology, physiology, Phosphatidylinositol 3-Kinases, antagonists & inhibitors, Protease Inhibitors, Recombinant Proteins, Signal Transduction, Tissue Inhibitor of Metalloproteinase-1, ras Proteins

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          Abstract

          Tissue inhibitor of metalloproteinases-1 (TIMP-1) is a multifunctional protein, which is found in most tissues and body fluids. Here, we demonstrated that recombinant TIMP-1 but not the synthetic matrix metalloproteinase inhibitor, GM6001, stimulated proliferation of human aortic smooth muscle cells (AoSMC) in a dose-dependent manner. The mitogenic effect was associated with activation of Ras, increased phosphorylation of ERK, and stimulation of cyclin D1 expression. The phosphatidylinositol 3-kinase (PI3K) signaling pathway was also involved since the PI3K inhibitor, LY294002, abolished the TIMP-1-mediated growth stimulation. These data suggest that TIMP-1 activates Ras, which then turns on the ERK and PI3K signaling pathways to promote cell cycle progression of the AoSMC.

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