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      Sequential activation of phosphatidylinositol 3-kinase, beta Pix, Rac1, and Nox1 in growth factor-induced production of H2O2.

      Molecular and Cellular Biology
      Animals, Base Sequence, COS Cells, Caco-2 Cells, Cell Cycle Proteins, genetics, metabolism, Cell Line, Epidermal Growth Factor, pharmacology, Guanine Nucleotide Exchange Factors, Humans, Hydrogen Peroxide, Mutation, NADPH Oxidase, Phosphatidylinositol 3-Kinases, RNA, Small Interfering, Reactive Oxygen Species, Recombinant Fusion Proteins, Rho Guanine Nucleotide Exchange Factors, Transfection, rac1 GTP-Binding Protein

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          Abstract

          The generation of reactive oxygen species (ROS) in cells stimulated with growth factors requires the activation of phosphatidylinositol 3-kinase (PI3K) and the Rac protein. We report here that the COOH-terminal region of Nox1, a protein related to gp91(phox) (Nox2) of phagocytic cells, is constitutively associated with beta Pix, a guanine nucleotide exchange factor for Rac. Both growth factor-induced ROS production and Rac1 activation were completely blocked in cells depleted of beta Pix by RNA interference. Rac1 was also shown to bind to the COOH-terminal region of Nox1 in a growth factor-dependent manner. Moreover, the depletion of Nox1 by RNA interference inhibited growth factor-induced ROS generation. These results suggest that ROS production in growth factor-stimulated cells is mediated by the sequential activation of PI3K, beta Pix, and Rac1, which then binds to Nox1 to stimulate its NADPH oxidase activity.

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