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      Essential role for the p110delta phosphoinositide 3-kinase in the allergic response.

      Nature
      Anaphylaxis, enzymology, immunology, Animals, Cell Adhesion, drug effects, Cell Count, Cell Degranulation, Cell Movement, Cytokines, metabolism, Dermis, cytology, Genes, Essential, genetics, Humans, Hypersensitivity, Interleukin-3, pharmacology, Isoenzymes, antagonists & inhibitors, Mast Cells, Mice, Mice, Inbred BALB C, Mice, Inbred C57BL, Phosphatidylinositol 3-Kinases, Receptors, IgE, Second Messenger Systems, physiology, Stem Cell Factor

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          Abstract

          Inflammatory substances released by mast cells induce and maintain the allergic response. Mast cell differentiation and activation are regulated, respectively, by stem cell factor (SCF; also known as Kit ligand) and by allergen in complex with allergen-specific immunoglobulin E (IgE). Activated SCF receptors and high-affinity receptors for IgE (FcvarepsilonRI) engage phosphoinositide 3-kinases (PI(3)Ks) to generate intracellular lipid second messenger signals. Here, we report that genetic or pharmacological inactivation of the p110delta isoform of PI(3)K in mast cells leads to defective SCF-mediated in vitro proliferation, adhesion and migration, and to impaired allergen-IgE-induced degranulation and cytokine release. Inactivation of p110delta protects mice against anaphylactic allergic responses. These results identify p110delta as a new target for therapeutic intervention in allergy and mast-cell-related pathologies.

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