Dynamic control of neuroexocytosis by phosphoinositides in health and disease

被引:15
作者
Wen, P. J.
Osborne, S. L.
Meunier, F. A. [1 ]
机构
[1] Univ Queensland, Queensland Brain Inst, Neuronal Trafficking Lab, Brisbane, Qld 4072, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
Phosphoinositides; Phosphoinositides signalling; Exocytosis; Actin; Neurodegenerative diseases; PHOSPHATIDYLINOSITOL; 3-PHOSPHATE; 5-KINASE; MYOTUBULARIN-RELATED PROTEIN-2; ADRENAL CHROMAFFIN CELLS; MARIE-TOOTH-DISEASE; INOSITOL POLYPHOSPHATE 4-PHOSPHATASE; PLECKSTRIN HOMOLOGY DOMAIN; PLASMA-MEMBRANE; SECRETORY GRANULES; CA2+-ACTIVATED SECRETION; SUBCELLULAR-LOCALIZATION;
D O I
10.1016/j.plipres.2010.08.001
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
Phosphoinositides are a group of phospholipids whose inositol headgroups can be phosphorylated at three distinct positions thereby generating seven different isotypes. The conversion between these lipid species depends on the activity of specific sets of phosphoinositide kinases and phosphatases whose targeting and activity is critical to establish the landscape of phosphoinositides on the cytosol-facing hemi-membrane of all organelles and plasmalemma. Phosphoinositides play pleiotropic roles ranging from signalling and membrane trafficking to modulation of ion channels and survival. In neurons and neurosecretory cells, whose main function is to communicate through the release of neurotransmitter. most of the work has focused on the role played by phosphatidylinositol (4,5) bisphosphate in controlling the mechanism underpinning neurotransmitter release through the fusion of secretory vesicles with the plasmalemma. Emerging evidence supports a multi-faceted regulation of neuroexocytosis by 3-phosphorylated phosphoinositides. In this review, we summarise the molecular mechanism by which these lipids control exocytosis and how minute changes in their metabolism can have devastating effects in the nervous system and lead to neurodegeneration. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:52 / 61
页数:10
相关论文
共 158 条
[61]   Synaptojanin-1 plays a key role in astrogliogenesis: possible relevance for Down's syndrome [J].
Herrera, F. ;
Chen, Q. ;
Fishcer, W. H. ;
Maher, P. ;
Schubert, D. R. .
CELL DEATH AND DIFFERENTIATION, 2009, 16 (06) :910-920
[62]   Activation by Cdc42 and PIP2 of Wiskott-Aldrich syndrome protein (WASp) stimulates actin nucleation by Arp2/3 complex [J].
Higgs, HN ;
Pollard, TD .
JOURNAL OF CELL BIOLOGY, 2000, 150 (06) :1311-1320
[63]   EFFECTS OF ACETYLCHOLINE ON PHOSPHATE TURNOVER IN PHOSPHOLIPIDES OF BRAIN CORTEX INVITRO [J].
HOKIN, LE ;
HOKIN, MR .
BIOCHIMICA ET BIOPHYSICA ACTA, 1955, 16 (02) :229-237
[64]   EFFECTS OF ACETYLCHOLINE ON THE TURNOVER OF PHOSPHORYL UNITS IN INDIVIDUAL PHOSPHOLIPIDS OF PANCREAS SLICES AND BRAIN CORTEX SLICES [J].
HOKIN, LE ;
HOKIN, MR .
BIOCHIMICA ET BIOPHYSICA ACTA, 1955, 18 (01) :102-110
[65]   THE EFFECTS OF ACETYLCHOLINE ON THE TURNOVER OF PHOSPHATIDIC ACID AND PHOSPHOINOSITIDE IN SYMPATHETIC GANGLIA, AND IN VARIOUS PARTS OF THE CENTRAL NERVOUS SYSTEM INVITRO [J].
HOKIN, MR ;
HOKIN, LE ;
SHELP, WD .
JOURNAL OF GENERAL PHYSIOLOGY, 1960, 44 (02) :217-226
[66]  
HOKIN MR, 1954, J BIOL CHEM, V209, P549
[67]   A pleckstrin homology domain specific for phosphatidylinositol 4,5-bisphosphate (PtdIns-4,5-P2) and fused to green fluorescent protein identifies plasma membrane PtdIns-4,5-P2 as being important in exocytosis [J].
Holz, RW ;
Hlubek, MD ;
Sorensen, SD ;
Fisher, SK ;
Balla, T ;
Ozaki, S ;
Prestwich, GD ;
Stuenkel, EL ;
Bittner, MA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (23) :17878-17885
[68]   Inhibition of quantal release from motor nerve by wortmannin [J].
Hong, SJ ;
Chang, CC .
BRITISH JOURNAL OF PHARMACOLOGY, 1999, 128 (01) :142-148
[69]   ArPIKfyve-PIKfyve interaction and role in insulin-regulated GLUT4 translocation and glucose transport in 3T3-L1 adipocytes [J].
Ikonomov, Nian C. ;
Sbrissa, Diego ;
Dondapati, Rajeswari ;
Shisheva, Assia .
EXPERIMENTAL CELL RESEARCH, 2007, 313 (11) :2404-2416
[70]   Requirement for PIKfyve enzymatic activity in acute and long-term insulin cellular effects [J].
Ikonomov, OC ;
Sbrissa, D ;
Mlak, K ;
Shisheva, A .
ENDOCRINOLOGY, 2002, 143 (12) :4742-4754