Protein kinase B kinases that mediate phosphatidylinositol 3,4,5-Triphosphate-dependent activation of protein kinase B

• Published in: Science (American Association for the Advancement of Science) 1998-01, Vol.279 (5351), p.710
• Main Authors: Stephens, Len, Anderson, Karen, Stokoe, David, Erdjument-Bromage, Hediye, Painter, Gavin F, Holmes, Andrew B, Gaffney, Piers R, Reese, Colin B, McCormick, Frank, Tempst, Paul, Coadwell, J, Hawkins, Phillip T
• Format: Article
• Language: English
• Subjects: Cell receptors; Cellular signal transduction; Observations; Proteins; Receptors
• ISSN: 0036-8075; 1095-9203

Protein kinase B (PKB) is activated in response to phosphoinositide 3-kinases and their lipid products phosphatidylinositol 3,4,5-trisphosphate [PtdIns(3,4,5)[P.sub.3]] and PtdIns(3,4)[P.sub.2] in the signaling pathways used by a wide variety of growth factors, antigens, and inflammatory stimuli. PKB is a direct target of these lipids, but this regulation is complex. The lipids can bind to the pleckstrin homologous domain of PKB, causing its translocation to the membrane, and also enable upstream, [Thr.sup.308]-directed kinases to phosphorylate and activate PKB. Four isoforms of these PKB kinases were purified from sheep brain. They bound PtdIns(3,4,5)[P.sub.3] and associated with lipid vesicles containing it. These kinases contain an [NH.sub.2]-terminal catalytic domain and a COOH-terminal pleckstrin homologous domain, and their heterologous expression augments receptor activation of PKB, which suggests they are the primary signal transducers that enable PtdIns(3,4,5)[P.sub.3] or PtdIns(3,4)[P.sub.2] to activate PKB and hence to control signaling pathways regulating cell survival, glucose uptake, and glycogen metabolism.