Literature DB >> 21220345

Inositol polyphosphate multikinase is a physiologic PI3-kinase that activates Akt/PKB.

David Maag1, Micah J Maxwell, Douglas A Hardesty, Katie L Boucher, Namrata Choudhari, Adam G Hanno, Jenny F Ma, Adele S Snowman, Joseph W Pietropaoli, Risheng Xu, Phillip B Storm, Adolfo Saiardi, Solomon H Snyder, Adam C Resnick.   

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.

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Year:  2011        PMID: 21220345      PMCID: PMC3029688          DOI: 10.1073/pnas.1017831108

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  35 in total

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