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Inositol polyphosphate multikinase is a physiologic PI3-kinase that activates Akt/PKB.
- Source :
-
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2011 Jan 25; Vol. 108 (4), pp. 1391-6. Date of Electronic Publication: 2011 Jan 10. - Publication Year :
- 2011
-
Abstract
- The second messenger phosphatidylinositol (3,4,5)-trisphosphate (PIP(3)), formed by the p110 family of PI3-kinases, promotes cellular growth, proliferation, and survival, in large part by activating the protein kinase Akt/PKB. We show that inositol polyphosphate multikinase (IPMK) physiologically generates PIP(3) as well as water soluble inositol phosphates. IPMK deletion reduces growth factor-elicited Akt signaling and cell proliferation caused uniquely by loss of its PI3-kinase activity. Inhibition of p110 PI3-kinases by wortmannin prevents IPMK phosphorylation and activation. Thus, growth factor stimulation of Akt signaling involves PIP(3) generation through the sequential activations of the p110 PI3-kinases and IPMK. As inositol phosphates inhibit Akt signaling, IPMK appears to act as a molecular switch, inhibiting or stimulating Akt via its inositol phosphate kinase or PI3-kinase activities, respectively. Drugs regulating IPMK may have therapeutic relevance in influencing cell proliferation.
- Subjects :
- Androstadienes pharmacology
Animals
Cell Line, Tumor
Cell Proliferation drug effects
Cells, Cultured
Embryo, Mammalian cytology
Enzyme Activation drug effects
Female
Fibroblasts cytology
Fibroblasts drug effects
HEK293 Cells
Humans
Immunoblotting
Inositol Phosphates metabolism
Intercellular Signaling Peptides and Proteins pharmacology
Male
Mice
Mice, 129 Strain
Mice, Inbred C57BL
Mice, Knockout
Models, Biological
Phosphatidylinositol 3-Kinases genetics
Phosphatidylinositol Phosphates metabolism
Phosphoinositide-3 Kinase Inhibitors
Phosphorylation drug effects
Phosphotransferases (Alcohol Group Acceptor) genetics
Wortmannin
Fibroblasts metabolism
Phosphatidylinositol 3-Kinases metabolism
Phosphotransferases (Alcohol Group Acceptor) metabolism
Proto-Oncogene Proteins c-akt metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1091-6490
- Volume :
- 108
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Publication Type :
- Academic Journal
- Accession number :
- 21220345
- Full Text :
- https://doi.org/10.1073/pnas.1017831108