Phosphoinositides - Key players in cell signalling, in time and space

被引:182
作者
Payrastre, B [1 ]
Missy, K [1 ]
Giuriato, S [1 ]
Bodin, S [1 ]
Plantavid, M [1 ]
Gratacap, MP [1 ]
机构
[1] Hop Purpan, INSERM, U326, IFR 30, F-31059 Toulouse, France
关键词
phosphoinositide; cell signalling; Pi-kinases; subcellular organization;
D O I
10.1016/S0898-6568(01)00158-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Over the last few years, many reports have extended our knowledge of the inositol lipid metabolism and brought out some exciting information about the location, the variety and the role of phosphoinositides (PIs). Besides the so-called "canonical PI pathway" leading to the production of phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P-2), the precursor of the intracellular second messengers inositol 1,4,5- trisphosphate and diacylglycerol (DAG), many other metabolic pathways have been identified to produce seven different polyphosphoinositides. Several of these quantitatively minor lipid molecules appear to be specifically involved in the control of cellular events, such as the spatial and temporal organisation of key signalling pathways, the rearrangement of the actin cytoskeleton or the intracellular vesicle trafficking. This is consistent with the fact that many of the enzymes, such as kinases and phosphatases, involved in the tight control of the intracellular level of polyphosphoinositides, are regulated and/or relocated through cell surface receptors for extracellular ligands. The remarkable feature of PIs, which can be rapidly synthesised and degraded in discrete membrane domains or even subnuclear structures, places them as ideal regulators and integrators of very dynamic mechanisms of cell regulation. In this review we will summarise recent studies on the potential location, the metabolic pathways and the role of the different PIs. Some aspects of the temporal synthesis of D3 PIs will also be discussed. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:377 / 387
页数:11
相关论文
共 109 条
[1]   Constitutive macropinocytosis in oncogene-transformed fibroblasts depends on sequential permanent activation of phosphoinositide 3-kinase and phospholipase C [J].
Amyere, M ;
Payrastre, B ;
Krause, U ;
Van Der Smissen, P ;
Veithen, A ;
Courtoy, PJ .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (10) :3453-3467
[2]   Phosphatidylinositol phosphate kinases, a multifaceted family of signaling enzymes [J].
Anderson, RA ;
Boronenkov, IV ;
Doughman, SD ;
Kunz, J ;
Loijens, JC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (15) :9907-9910
[3]   PDGF-DEPENDENT TYROSINE PHOSPHORYLATION STIMULATES PRODUCTION OF NOVEL POLYPHOSPHOINOSITIDES IN INTACT-CELLS [J].
AUGER, KR ;
SERUNIAN, LA ;
SOLTOFF, SP ;
LIBBY, P ;
CANTLEY, LC .
CELL, 1989, 57 (01) :167-175
[4]  
BACQUEVILLE D, 1999, FEBS 99, P172
[5]   How accurately can we image inositol lipids in living cells? [J].
Balla, T ;
Bondeva, T ;
Várnai, P .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2000, 21 (07) :238-241
[6]   Isolation and molecular cloning of wortmannin-sensitive bovine type III phosphatidylinositol 4-kinases [J].
Balla, T ;
Downing, GJ ;
Jaffe, H ;
Kim, S ;
Zolyomi, A ;
Catt, KJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (29) :18358-18366
[7]   Mutagenesis of the phosphatidylinositol 4,5-bisphosphate (PIP2) binding site in the NH2-terminal domain of ezrin correlates with its altered cellular distribution [J].
Barret, C ;
Roy, C ;
Montcourrier, P ;
Mangeat, P ;
Niggli, V .
JOURNAL OF CELL BIOLOGY, 2000, 151 (05) :1067-1079
[8]   A novel link between integrins, transmembrane-4 superfamily proteins (CD63 and CD81), and phosphatidylinositol 4-kinase [J].
Berditchevski, F ;
Tolias, KF ;
Wong, K ;
Carpenter, CL ;
Hemler, ME .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (05) :2595-2598
[9]   INOSITOL TRISPHOSPHATE AND DIACYLGLYCEROL AS 2ND MESSENGERS [J].
BERRIDGE, MJ .
BIOCHEMICAL JOURNAL, 1984, 220 (02) :345-360
[10]  
BERRIDGE MJ, 1987, ANNU REV BIOCHEM, V56, P159, DOI 10.1146/annurev.bi.56.070187.001111