The multiple roles of PtdIns(4)P -: not just the precursor of PtdIns(4,5)P2

被引:176
作者
D'Angelo, Giovanni [1 ]
Vicinanza, Mariella [1 ]
Di Campli, Antonella [1 ]
De Matteis, Maria Antonietta [1 ]
机构
[1] Consorzio Mario Negri Sud, Dept Cell Biol & Oncol, Lab Secret Physiopathol, I-66030 Santa Maria Imbaro, CH, Italy
关键词
phosphoinositides; PtdIns(4)P; PtdIns(4)P-binding proteins; PI; 4-kinase; Golgi complex; lipid-transfer protein;
D O I
10.1242/jcs.023630
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The phosphoinositides (PIs) are membrane phospholipids that actively operate at membrane-cytosol interfaces through the recruitment of a number of effector proteins. In this context, each of the seven different PI species represents a topological determinant that can establish the nature and the function of the membrane where it is located. Phosphatidylinositol 4-phosphate (PtdIns(4)P) is the most abundant of the monophosphorylated inositol phospholipids in mammalian cells, and it is produced by D-4 phosphorylation of the inositol ring of PtdIns. PtdIns(4)P can be further phosphorylated to PtdIns(4,5)P-2 by PtdIns(4)P 5-kinases and, indeed, PtdIns(4)P has for many years been considered to be just the precursor of PtdIns(4,5) P-2. Over the last decade, however, a large body of evidence has accumulated that shows that PtdIns(4)P is, in its own right, a direct regulator of important cell functions. The subcellular localisation of the PtdIns(4)P effectors initially led to the assumption that the bulk of this lipid is present in the membranes of the Golgi complex. However, the existence and physiological relevance of 'non-Golgi pools' of PtdIns(4)P have now begun to be addressed. The aim of this Commentary is to describe our present knowledge of PtdIns(4)P metabolism and the molecular machineries that are directly regulated by PtdIns(4)P within and outside of the Golgi complex.
引用
收藏
页码:1955 / 1963
页数:9
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[1]   Distinct roles for the yeast phosphatidylinositol 4-kinases, Stt4p and Pik1p, in secretion, cell growth, and organelle membrane dynamics [J].
Audhya, A ;
Foti, M ;
Emr, SD .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (08) :2673-2689
[2]   Stt4 PI 4-kinase localizes to the plasma membrane and functions in the Pkc1-mediated MAP kinase cascade [J].
Audhya, A ;
Emr, SD .
DEVELOPMENTAL CELL, 2002, 2 (05) :593-605
[3]   A plasma membrane pool of phosphatidylinositol 4-phosphate is generated by phosphatidylinositol 4-kinase type-III alpha:: Studies with the PH domains of the oxysterol binding protein and FAPP1 [J].
Balla, A ;
Tuymetova, G ;
Tsiomenko, A ;
Várnai, P ;
Balla, T .
MOLECULAR BIOLOGY OF THE CELL, 2005, 16 (03) :1282-1295
[4]   Characterization of type II phosphatidylinositol 4-kinase isoforms reveals association of the enzymes with endosomal vesicular compartments [J].
Balla, A ;
Tuymetova, G ;
Barshishat, M ;
Geiszt, M ;
Balla, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (22) :20041-20050
[5]   Phosphatidylinositol 4-kinases: old enzymes with emerging functions [J].
Balla, Andras ;
Balla, Tamas .
TRENDS IN CELL BIOLOGY, 2006, 16 (07) :351-361
[6]   Maintenance of hormone-sensitive phosphoinositide pools in the plasma membrane requires phosphatidylinositol 4-kinase IIIα [J].
Balla, Andras ;
Kim, Yeun Ju ;
Varnai, Peter ;
Szentpetery, Zsofia ;
Knight, Zachary ;
Shokat, Kevan M. ;
Balla, Tamas .
MOLECULAR BIOLOGY OF THE CELL, 2008, 19 (02) :711-721
[7]   Role of diacylglycerol in PKD recruitment to the TGN and protein transport to the plasma membrane [J].
Baron, CL ;
Malhotra, V .
SCIENCE, 2002, 295 (5553) :325-328
[8]   Phosphatidylinositol 4-phosphate formation at ER exit sites regulates ER export [J].
Blumental-Perry, Anna ;
Haney, Charles J. ;
Weixel, Kelly M. ;
Watkins, Simon C. ;
Weisz, Ora A. ;
Aridor, Meir .
DEVELOPMENTAL CELL, 2006, 11 (05) :671-682
[9]   A WASp-binding type II phosphatidylinositol 4-kinase required for actin polymerization-driven endosome motility [J].
Chang, FS ;
Han, GS ;
Carman, GM ;
Blumer, KJ .
JOURNAL OF CELL BIOLOGY, 2005, 171 (01) :133-142
[10]   Epsin is an EH-domain-binding protein implicated in clathrin-mediated endocytosis [J].
Chen, H ;
Fre, S ;
Slepnev, VI ;
Capua, MR ;
Takei, K ;
Butler, MH ;
Di Fiore, PP ;
De Camilli, P .
NATURE, 1998, 394 (6695) :793-797