Critical role for lipid raft-associated Src kinases in activation of PI3K-Akt signalling

被引:115
作者
Arcaro, Alexandre
Aubert, Muriel
del Hierro, Maria E. Espinosa
Khanzada, Umme K.
Angelidou, Smaragda
Tetley, Teresa D.
Bittermann, Anne G.
Frame, Margaret C.
Seckl, Michael J.
机构
[1] Univ Zurich, Dept Pediat, Div Clin Chem & Biochem, CH-8032 Zurich, Switzerland
[2] Univ London Imperial Coll Sci Technol & Med, Div Med, Lung Canc Biol Grp, London W12 0NN, England
[3] Univ London Imperial Coll Sci Technol & Med, Fac Med, Natl Heart & Lung Inst, London SW3 6LY, England
[4] Univ Zurich, Elektronenmikroskop Zentrallabor, CH-8006 Zurich, Switzerland
[5] Canc Res UK Beatson Labs, Beatson Inst Canc Res, Glasgow G61 1BD, Lanark, Scotland
关键词
lung cancer; c-kit; lipid rafts; phosphoinositide; 3-kinase; protein kinase B/Akt; Src;
D O I
10.1016/j.cellsig.2006.12.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Lipid rafts are membrane microdomains distinct from caveolae, whose functions in polypeptide growth factor signalling remain unclear. Here we show that in small cell lung cancer (SCLC) cells, specific growth factor receptors such as c-Kit associate with lipid rafts and that these domains play a critical role in the activation of phosphoinositide 3-kinase (PI3K) signalling. The class I(A) p85/p110 alpha associated with Src in lipid rafts and was activated by Src in vitro. Lipid raft integrity was essential for Src activation in response to stein cell factor (SCF) and raft disruption selectively inhibited activation of protein kinase B (PKB)/Akt in response to SCF stimulation. Moreover, inhibition of Src kinases blocked PKB/ Akt activation and SCLC cell growth. The use of fibroblasts with targeted deletion of the Src family kinase genes confirmed the role of Src kinases in PKB/Akt activation by growth factor receptors. Moreover a constitutively activated mutant of Src also stimulated PI3K/Akt in lipid rafts, indicating that these microdomains play a role in oncogenic signalling. Together our data demonstrate that lipid rafts play a key role in the activation of PI3K signalling by facilitating the interaction of Src with specific PI3K isoforms. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1081 / 1092
页数:12
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