Abstract
Class IA phosphoinositide 3-kinases (PI3Ks) are a family of p85/p110 heterodimeric lipid kinases that generate second messenger signals downstream of tyrosine kinases, thereby controlling cell metabolism, growth, proliferation, differentiation, motility, and survival. Mammals express three class IA catalytic subunits: p110alpha, p110beta, and p110delta. It is unclear to what extent these p110 isoforms have overlapping or distinct biological roles. Mice expressing a catalytically inactive form of p110delta (p110delta(D910A)) were generated by gene targeting. Antigen receptor signaling in B and T cells was impaired and immune responses in vivo were attenuated in p110delta mutant mice. They also developed inflammatory bowel disease. These results reveal a selective role for p110delta in immunity.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Antigens / immunology
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B-Lymphocytes / enzymology
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B-Lymphocytes / immunology*
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Bone Marrow Cells / cytology
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Catalytic Domain
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Cell Differentiation
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Cell Division
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Class I Phosphatidylinositol 3-Kinases
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Female
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Gene Targeting
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Hematopoietic Stem Cells / cytology
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Immunoglobulins / blood
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Inflammatory Bowel Diseases / immunology
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Inflammatory Bowel Diseases / pathology
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Interleukin-2 / biosynthesis
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Intestinal Mucosa / pathology
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Lymph Nodes / cytology
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Lymph Nodes / pathology
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Lymphocyte Activation
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Male
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Mice
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Mice, Inbred C57BL
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Phosphatidylinositol 3-Kinases / genetics
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Phosphatidylinositol 3-Kinases / metabolism*
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Point Mutation
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Protein Serine-Threonine Kinases*
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Proto-Oncogene Proteins / metabolism
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Proto-Oncogene Proteins c-akt
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Receptors, Antigen, B-Cell / metabolism*
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Receptors, Antigen, T-Cell / metabolism*
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Signal Transduction
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Spleen / cytology
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Spleen / pathology
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T-Lymphocytes / enzymology
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T-Lymphocytes / immunology*
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Thymus Gland / cytology
Substances
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Antigens
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Immunoglobulins
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Interleukin-2
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Proto-Oncogene Proteins
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Receptors, Antigen, B-Cell
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Receptors, Antigen, T-Cell
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Class I Phosphatidylinositol 3-Kinases
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Pik3cd protein, mouse
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Protein Serine-Threonine Kinases
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Proto-Oncogene Proteins c-akt