Enrichment of phosphatidylinositols with specific acyl chains

被引:74
作者
D'Souza, Kenneth [1 ]
Epand, Richard M. [1 ]
机构
[1] McMaster Univ, Dept Biochem & Biomed Sci, Hamilton, ON L8S 4K1, Canada
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2014年 / 1838卷 / 06期
基金
加拿大自然科学与工程研究理事会;
关键词
Phosphatidylinositol; Phosphatidylinositol cycle; Arachidonoyl; Lipid signal; Acyl chain; DIACYLGLYCEROL-KINASE-EPSILON; 4-PHOSPHATE 5-KINASE ALPHA; PHOSPHATIDIC-ACID; ARACHIDONIC-ACID; FATTY-ACIDS; RAT-LIVER; PHOSPHOLIPASE-A; METABOLISM; BRAIN; SUBSTRATE;
D O I
10.1016/j.bbamem.2013.10.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
There are six major species of phospholipids in eukaryotes, each of which plays unique structural and functional roles. One species, phosphatidylinositol (PI) only contributes about 2-10% of the total phospholipid pool. However, they are critical factors in the regulation of several fundamental processes such as in membrane dynamics and signal transduction pathways. Although numerous acyl species exist, PI species are enriched with one specific acyl chain composition at both sn -1 and sn -2 positions. Recent work has identified several enzymes that act on lipids to lead to the formation or interconversion of PI species that exhibit acyl chain specificity. These enzymes contribute to this lipid's enrichment with specific acyl chains. The nature of the acyl chains on signaling lipids has been shown to contribute to their specificity. Here we review some of the critical functions of PI and the multiple pathways in which PI can be produced and metabolized. We also discuss a common motif that may confer arachidonoyl specificity to several of the enzymes involved. This article is part of a Special Issue entitled: Membrane Structure and Function: Relevance in the Cell's Physiology, Pathology and Therapy. (C) 2013 Elsevier S.V. All rights reserved.
引用
收藏
页码:1501 / 1508
页数:8
相关论文
共 94 条
[1]
Antidepressant stimulation of CDP-diacylglycerol synthesis does not require monoamine reuptake inhibition [J].
Aboukhatwa, Marwa A. ;
Undieh, Ashiwel S. .
BMC NEUROSCIENCE, 2010, 11
[2]
Lysophosphatidylinositol-Acyltransferase-1 (LPIAT1) Is Required to Maintain Physiological Levels of PtdIns and PtdInsP2 in the Mouse [J].
Anderson, Karen E. ;
Kielkowska, Anna ;
Durrant, Tom N. ;
Juvin, Veronique ;
Clark, Jonathan ;
Stephens, Len R. ;
Hawkins, Phillip T. .
PLOS ONE, 2013, 8 (03)
[3]
Structure and function of phosphatidylserine-specific phospholipase A1 [J].
Aoki, J ;
Nagai, Y ;
Hosono, H ;
Inoue, K ;
Arai, H .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2002, 1582 (1-3) :26-32
[4]
Phosphatidic acid, a key intermediate in lipid metabolism [J].
Athenstaedt, K ;
Daum, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 266 (01) :1-16
[6]
Inositol-lipid binding motifs: signal integrators through protein-lipid and protein-protein interactions [J].
Balla, T .
JOURNAL OF CELL SCIENCE, 2005, 118 (10) :2093-2104
[7]
Lipid signaling in neural plasticity, brain repair, and neuroprotection [J].
Bazan, NG .
MOLECULAR NEUROBIOLOGY, 2005, 32 (01) :89-103
[8]
Neuroinflammation and Proteostasis are Modulated by Endogenously Biosynthesized Neuroprotectin D1 [J].
Bazan, Nicolas G. .
MOLECULAR NEUROBIOLOGY, 2012, 46 (01) :221-226
[9]
ROLE OF PHOSPHOLIPIDS IN ENDOCYTOSIS, PHAGOCYTOSIS, AND MACROPINOCYTOSIS [J].
Bohdanowicz, Michal ;
Grinstein, Sergio .
PHYSIOLOGICAL REVIEWS, 2013, 93 (01) :69-106
[10]
Diacylglycerol kinases as sources of phosphatidic acid [J].
Cai, Jinjin ;
Abramovici, Hanan ;
Gee, Stephen H. ;
Topham, Matthew K. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2009, 1791 (09) :942-948