Metabolism and biological functions of two phosphorylated sphingolipids, sphingosine 1-phosphate and ceramide 1-phosphate

被引:147
作者
Kihara, Akio
Mitsutake, Susumu
Mizutani, Yukiko
Igarashi, Yasuyuki
机构
[1] Hokkaido Univ, Fac Pharmaceut Sci, Lab Biomembrane & Biofunct Chem, Kita Ku, Sapporo, Hokkaido 0600812, Japan
[2] Hokkaido Univ, Fac Adv Life Sci, Lab Biomembrane & Biofunct Chem, Kita Ku, Sapporo, Hokkaido 0010021, Japan
关键词
ceramide; 1-phosphate; ceramide kinase; long-chain base 1-phosphate; sphingolipid; sphingosine kinase; sphingosine;
D O I
10.1016/j.plipres.2007.03.001
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
Sphingolipids are major lipid constituents of the eukaryotic plasma membrane. Without certain sphingolipids, cells and/ or embryos cannot survive, indicating that sphingolipids possess important physiological functions that are not substituted for by other lipids. One such role may be signaling. Recent studies have revealed that some sphingolipid metabolites, such as long-chain bases (LCBs; sphingosine (Sph) in mammals), long-chain base I-phosphates (LCBPs; sphingosine I-phosphate (S1P) in mammals), ceramide (Cer), and ceramide 1-phosphate (C1P), act as signaling molecules. The addition of phosphate groups to LCB/Sph and Cer generates LCBP/S1P and C1P, respectively. These phospholipids exhibit completely different functions than those of their precursors. In this review, we describe recent advances in understanding the functions of LCBP/S1P and C1P in mammals and in the yeast Saccharomyces cerevisiae. Since LCB/Sph, LCBP/S1P, Cer, and C1P are mutually convertible, regulation of not only the total amount of the each lipid but also of the overall balance in cellular levels is important. Therefore, we describe in detail their metabolic pathways, as well as the genes involved in each reaction. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:126 / 144
页数:19
相关论文
共 217 条
[11]   Calcium influx and signaling in yeast stimulated by intracellular sphingosine 1-phosphate accumulation [J].
Birchwood, CJ ;
Saba, JD ;
Dickson, RC ;
Cunningham, KW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (15) :11712-11718
[12]  
BOUDKER O, 1993, J BIOL CHEM, V268, P22150
[13]   Structure of the skin barrier and its modulation by vesicular formulations [J].
Bouwstra, JA ;
Honeywell-Nguyen, PL ;
Gooris, GS ;
Ponec, M .
PROGRESS IN LIPID RESEARCH, 2003, 42 (01) :1-36
[14]   Mammalian lipid phosphate phosphohydrolases [J].
Brindley, DN ;
Waggoner, DW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (38) :24281-24284
[15]  
Brindley DN, 2000, METHOD ENZYMOL, V311, P233
[16]   The immune modulator FTY720 targets sphingosine 1-phosphate receptors [J].
Brinkmann, V ;
Davis, MD ;
Heise, CE ;
Albert, R ;
Cottens, S ;
Hof, R ;
Bruns, C ;
Prieschl, E ;
Baumruker, T ;
Hiestand, P ;
Foster, CA ;
Zollinger, M ;
Lynch, KR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (24) :21453-21457
[17]   FTY720: Mechanism of action and potential benefit in organ transplantation [J].
Brinkmann, V .
YONSEI MEDICAL JOURNAL, 2004, 45 (06) :991-997
[18]   Ceramide kinase targeting and activity determined by its N-terminal pleckstrin homology domain [J].
Carré, A ;
Graf, C ;
Stora, S ;
Mechtcheriakova, D ;
Csonga, R ;
Urtz, N ;
Billich, A ;
Baumruker, T ;
Bornancin, F .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 324 (04) :1215-1219
[19]   Sphingosine 1-phosphate and ceramide 1-phosphate: Expanding roles in cell signaling [J].
Chalfant, CE ;
Spiegel, S .
JOURNAL OF CELL SCIENCE, 2005, 118 (20) :4605-4612
[20]  
Choi OH, 1996, NATURE, V380, P634