SRC-dependent signalling regulates actin ruffle formation induced by glycerophosphoinositol 4-phosphate

被引:16
作者
Filippi, Beatrice Maria [1 ]
Mariggio, Stefania [1 ]
Pulvirenti, Teodoro [1 ]
Corda, Daniela [1 ]
机构
[1] Consorzio Mario Negri Sud, Dept Cell Biol & Oncol, I-66030 Chieti, Italy
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2008年 / 1783卷 / 12期
关键词
Glycerophosphoinositol; Phosphoinositide; Actin cytoskeleton; Signalling; Tyrosine kinase;
D O I
10.1016/j.bbamcr.2008.07.021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The glycerophosphoinositols are diffusible phosphoinositide metabolites reported to modulate actin dynamics and tumour cell spreading. In particular, the membrane permeant glycerophosphoinositol 4-phosphate (GroPIns4P) has been shown to act at the level of the small GTPase Rac1, to induce the rapid formation of membrane ruffles. Here, we have investigated the signalling cascade involved in this process, and show that it is initiated by the activation of Src kinase. In NIH3T3 cells, exogenous addition of GroPIns4P induces activation and translocation of Rac1 and its exchange factor TIAM1 to the plasma membrane: in addition, in in-vitro assays, GroPIns4P favours the formation of a protein complex that includes Rac1 and TIAM1. Neither of these processes involves direct actions of GroPIns4P on these proteins. Thus, through the use of specific inhibitors of tyrosine kinases and phospholipase C (and by direct evaluation of kinase activities and inositol 1,4,5-trisphosphate production), we show that GroPIns4P activates Src, and as a consequence, phospholipase C gamma and Ca2+/calmodulin kinase II, the last of which directly phosphorylates TIAM1 and leads to TIAM1/Rac1-dependent ruffle formation. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:2311 / 2322
页数:12
相关论文
共 72 条
[1]  
AKIYAMA T, 1987, J BIOL CHEM, V262, P5592
[2]   Rap1 promotes cell spreading by localizing Rac guanine nucleoticle exchange factors [J].
Arthur, WT ;
Quilliam, LA ;
Cooper, JA .
JOURNAL OF CELL BIOLOGY, 2004, 167 (01) :111-122
[3]   Activation of phospholipase C-γ by phosphatidylinositol 3,4,5-trisphosphate [J].
Bae, YS ;
Cantley, LG ;
Chen, CS ;
Kim, SR ;
Kwon, KS ;
Rhee, SG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (08) :4465-4469
[4]   The specificities of protein kinase inhibitors: an update [J].
Bain, J ;
McLauchlan, H ;
Elliott, M ;
Cohen, P .
BIOCHEMICAL JOURNAL, 2003, 371 :199-204
[5]   Src regulates distinct pathways for cell volume control through Vav and phospholipase Cγ [J].
Barfod, ET ;
Moore, AL ;
Melnick, RF ;
Lidofsky, SD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (27) :25548-25557
[6]   Coordinated regulation of platelet actin filament barbed ends by gelsolin and capping protein [J].
Barkalow, K ;
Witke, W ;
Kwiatkowski, DJ ;
Hartwig, JH .
JOURNAL OF CELL BIOLOGY, 1996, 134 (02) :389-399
[7]   Maintenance of PtdIns45P2 pools under limiting inositol conditions, as assessed by liquid chromatography-tandem mass spectrometry and PtdIns45P2 mass evaluation in Ras-transformed cells [J].
Berrie, CP ;
Dragani, LK ;
van der Kaay, J ;
Iurisci, C ;
Brancaccio, A ;
Rotilio, D ;
Corda, D .
EUROPEAN JOURNAL OF CANCER, 2002, 38 (18) :2463-2475
[8]   Membrane transport and in vitro metabolism of the Ras cascade messenger, glycerophosphoinositol 4-phosphate [J].
Berrie, CP ;
Iurisci, C ;
Corda, D .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 266 (02) :413-419
[9]  
BLEASDALE JE, 1990, J PHARMACOL EXP THER, V255, P756
[10]   Protein kinase C induces actin reorganization via a Src- and Rho-dependent pathway [J].
Brandt, D ;
Gimona, M ;
Hillmann, M ;
Haller, H ;
Mischak, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (23) :20903-20910