Thermotropic behavior and lateral distribution of very long chain sphingolipids

被引:31
作者
Bjorkqvist, Y. Jenny E. [1 ]
Brewer, Jonathan [2 ]
Bagatolli, Luis A. [2 ]
Slotte, J. Peter [1 ]
Westerlund, Bodil [1 ]
机构
[1] Abo Akad Univ, Dept Biochem & Pharm, SF-20500 Turku, Finland
[2] Univ So Denmark, Dept Biochem & Mol Biol, Membrane Biophys & Biophoton Grp, MEMPHYS Ctr Biomembrane Phys, Odense, Denmark
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2009年 / 1788卷 / 06期
基金
新加坡国家研究基金会; 芬兰科学院;
关键词
Cholesterol; Galactosylceramide; Glucosylceramide; Sphingomyelin; Differential scanning calorimetry; Fluorescence spectroscopy; N-ACYL SPHINGOMYELINS; DIFFERENTIAL SCANNING CALORIMETRY; X-RAY-DIFFRACTION; FATTY-ACIDS; PHASE-BEHAVIOR; MEMBRANE DOMAINS; LIPID-BILAYERS; GLYCOLIPID MEMBRANES; CELL-ADHESION; HEAD GROUPS;
D O I
10.1016/j.bbamem.2009.02.019
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 containing very long acyl chains are abundant in certain specialized tissues and minor components of plasma membranes in most mammalian cells. There are cellular processes in which these sphingolipids are required, and the function seems to be mediated through sphingolipid-rich membrane domains. This study was conducted to explore how very long acyl chains of sphingolipids influence their lateral distribution in membranes. Differential scanning calorimetry showed that 24:0- and 24:1-sphingomyelins, galactosylceramides and glucosylceramides exhibited complex thermotropic behavior and partial miscibility with palmitoyl sphingomyelin. The T-m was decreased by about 20 degrees C for all 24:1-sphingolipids compared to the corresponding 24:0-sphingolipids. The ability to pack tightly with ordered and extended acyl chains is a necessity for membrane lipids to partition into ordered domains in membranes and thus the 24:1-sphingolipids appeared less likely to do so. Fluorescence quenching measurements showed that the 24:0-sphingolipids formed ordered domains in multicomponent membranes, both as the only sphingolipid and mixed with palmitoyl sphingomyelin. These domains had a high packing density which appeared to hinder the partitioning of sterols into them, as reported by the fluorescent cholesterol analog cholestatrienol. 24:0-SM was, however, better able to accommodate sterol than the glycosphingolipids. The 24:1-sphingolipids could, depending on head group structure, either stabilize or disrupt ordered sphingolipid/cholesterol domains. We conclude that very long chain sphingolipids, when present in biological membranes, may affect the physical properties of or the distribution of sterols between lateral domains. It was also evident that not only the very long acyl chain but also the specific molecular structure of the sphingolipids was of importance for their membrane properties. (c) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1310 / 1320
页数:11
相关论文
共 64 条
[1]   Displacement of sterols from sterol/sphingomyelin domains in fluid bilayer membranes by competing molecules [J].
Alanko, SMK ;
Halling, KK ;
Maunula, S ;
Slotte, JP ;
Ramstedt, B .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2005, 1715 (02) :111-121
[2]  
ANGELOVA MI, 1992, PROG COLL POL SCI S, V89, P127
[3]   Two types of detergent-insoluble, glycosphingolipid/cholesterol-rich membrane domains from isolated myelin [J].
Arvanitis, DN ;
Min, WX ;
Gong, YP ;
Heng, YM ;
Boggs, JM .
JOURNAL OF NEUROCHEMISTRY, 2005, 94 (06) :1696-1710
[4]   THERMOTROPIC BEHAVIOR OF AQUEOUS DISPERSIONS OF GLUCOSYLCERAMIDE DIPALMITOYLPHOSPHATIDYLCHOLINE MIXTURES [J].
BARENHOLZ, Y ;
FREIRE, E ;
THOMPSON, TE ;
CORREAFREIRE, MC ;
BACH, D ;
MILLER, IR .
BIOCHEMISTRY, 1983, 22 (14) :3497-3501
[5]   N-palmitoyl-sulfatide participates in lateral domain formation in complex lipid bilayers [J].
Bjoerkqvist, Y. J. E. ;
Nybond, S. ;
Nyholm, T. K. M. ;
Slotte, J. P. ;
Ramstedt, B. .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2008, 1778 (04) :954-962
[6]   Domain formation and stability in complex lipid bilayers as reported by cholestatrienol [J].
Björkqvist, YJE ;
Nyholm, TKM ;
Slotte, JP ;
Ramstedt, B .
BIOPHYSICAL JOURNAL, 2005, 88 (06) :4054-4063
[7]   Distribution of cholesterol and galactosylceramide in rat cerebellar white matter [J].
Boerner, Katrin ;
Nygren, Hakan ;
Hagenhoff, Birgit ;
Malmberg, Per ;
Tallarek, Elke ;
Mansson, Jan-Eric .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2006, 1761 (03) :335-344
[8]   DO THE LONG FATTY-ACID CHAINS OF SPHINGOLIPIDS INTERDIGITATE ACROSS THE CENTER OF A BILAYER OF SHORTER CHAIN SYMMETRICAL PHOSPHOLIPIDS [J].
BOGGS, JM ;
KOSHY, KM .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1994, 1189 (02) :233-241
[9]   The membrane domains occupied by glycosylphosphatidylinositol-anchored prion protein and Thy-1 differ in lipid composition [J].
Brügger, B ;
Graham, C ;
Leibrecht, I ;
Mombelli, E ;
Jen, A ;
Wieland, F ;
Morris, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (09) :7530-7536
[10]   PREPARATION AND CHARACTERIZATION OF WELL DEFINED D-ERYTHRO SPHINGOMYELINS [J].
COHEN, R ;
BARENHOLZ, Y ;
GATT, S ;
DAGAN, A .
CHEMISTRY AND PHYSICS OF LIPIDS, 1984, 35 (04) :371-384