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磷脂酰肌醇-3激酶γ(PI3Kγ)的脂质和蛋白激酶信号向蛋白激酶B(PKB)和丝裂原活化蛋白激酶(MAPK)的分支。

Bifurcation of lipid and protein kinase signals of PI3Kgamma to the protein kinases PKB and MAPK.

作者信息

Bondeva T, Pirola L, Bulgarelli-Leva G, Rubio I, Wetzker R, Wymann M P

机构信息

Research Unit "Molecular Cell Biology," University of Jena, D-07747 Jena, Germany.

出版信息

Science. 1998 Oct 9;282(5387):293-6. doi: 10.1126/science.282.5387.293.

Abstract

Phosphoinositide 3-kinases (PI3Ks) activate protein kinase PKB (also termed Akt), and PI3Kgamma activated by heterotrimeric guanosine triphosphate-binding protein can stimulate mitogen-activated protein kinase (MAPK). Exchange of a putative lipid substrate-binding site generated PI3Kgamma proteins with altered or aborted lipid but retained protein kinase activity. Transiently expressed, PI3Kgamma hybrids exhibited wortmannin-sensitive activation of MAPK, whereas a catalytically inactive PI3Kgamma did not. Membrane-targeted PI3Kgamma constitutively produced phosphatidylinositol 3,4, 3,4,5-trisphosphate and activated PKB but not MAPK. Moreover, stimulation of MAPK in response to lysophosphatidic acid was blocked by catalytically inactive PI3Kgamma but not by hybrid PI3Kgammas. Thus, two major signals emerge from PI3Kgamma: phosphoinositides that target PKB and protein phosphorylation that activates MAPK.

摘要

磷酸肌醇3激酶(PI3Ks)激活蛋白激酶PKB(也称为Akt),并且由异三聚体鸟苷三磷酸结合蛋白激活的PI3Kγ可以刺激丝裂原活化蛋白激酶(MAPK)。一个假定的脂质底物结合位点的交换产生了具有改变或缺失脂质但保留蛋白激酶活性的PI3Kγ蛋白。瞬时表达时,PI3Kγ杂种表现出对渥曼青霉素敏感的MAPK激活,而催化无活性的PI3Kγ则没有。膜靶向的PI3Kγ组成性地产生磷脂酰肌醇3,4,3,4,5-三磷酸并激活PKB,但不激活MAPK。此外,催化无活性的PI3Kγ可阻断溶血磷脂酸对MAPK的刺激,而杂种PI3Kγ则不能。因此,PI3Kγ产生了两个主要信号:靶向PKB的磷酸肌醇和激活MAPK的蛋白磷酸化。

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