Lipid peroxidation induces cholesterol domain formation in model membranes

被引:127
作者
Jacob, RF
Mason, RP
机构
[1] Elucida Res, Beverly, MA 01915 USA
[2] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Med,Cardiovasc Div, Boston, MA 02115 USA
关键词
D O I
10.1074/jbc.M507587200
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
Numerous reports have established that lipid peroxidation contributes to cell injury by altering the basic physical properties and structural organization of membrane components. Oxidative modification of polyunsaturated phospholipids has been shown, in particular, to alter the intermolecular packing, thermodynamic, and phase parameters of the membrane bilayer. In this study, the effects of oxidative stress on membrane phospholipid and sterol organization were measured using small angle x-ray diffraction approaches. Model membranes enriched in dilinoleoylphosphatidylcholine were prepared at various concentrations of cholesterol and subjected to lipid peroxidation at physiologic conditions. At cholesterol-to-phospholipid mole ratios ( C/P) as low as 0.4, lipid peroxidation induced the formation of discrete, membrane-restricted cholesterol domains having a unit cell periodicity or d-space value of 34 angstrom. The formation of cholesterol domains correlated directly with lipid hydroperoxide levels and was inhibited by treatment with vitamin E. In the absence of oxidative stress, similar cholesterol domains were observed only at C/P ratios of 1.0 or higher. In addition to changes in sterol organization, lipid peroxidation also caused reproducible changes in overall membrane structure, including a 10 angstrom reduction in the width of the surrounding, sterol-poor membrane bilayer. These data provided direct evidence that lipid peroxidation alters the essential organization and structure of membrane lipids in a manner that may contribute to changes in membrane function during aging and oxidative stress-related disorders.
引用
收藏
页码:39380 / 39387
页数:8
相关论文
共 81 条
[1]   Effect of oxidation on Ca2+-ATPase activity and membrane lipids in lens epithelial microsomes [J].
Ahuja, RP ;
Borchman, D ;
Dean, WL ;
Paterson, CA ;
Zeng, J ;
Zhang, Z ;
Ferguson-Yankey, S ;
Yappert, MC .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 27 (1-2) :177-185
[2]   DIFFUSION OF UNIVALENT IONS ACROSS LAMELLAE OF SWOLLEN PHOSPHOLIPIDS [J].
BANGHAM, AD ;
STANDISH, MM ;
WATKINS, JC .
JOURNAL OF MOLECULAR BIOLOGY, 1965, 13 (01) :238-+
[3]   The role of oxidized lipoproteins in atherogenesis [J].
Berliner, JA ;
Heinecke, JW .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 20 (05) :707-727
[4]   LIPID-PEROXIDATION IN CATARACT OF THE HUMAN [J].
BHUYAN, KC ;
BHUYAN, DK ;
PODOS, SM .
LIFE SCIENCES, 1986, 38 (16) :1463-1471
[5]  
BIALECKI RA, 1989, AM J PHYSIOL, V257, P306
[6]   KINETIC DIFFERENCES BETWEEN CA2+-DEPENDENT K+ CHANNELS IN SMOOTH-MUSCLE CELLS ISOLATED FROM NORMAL AND ATHEROSCLEROTIC HUMAN AORTA [J].
BOLOTINA, V ;
GERICKE, M ;
BREGESTOVSKI, P .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1991, 244 (1309) :51-55
[7]   THE DUAL EFFECT OF OXIDATION ON LIPID BILAYER STRUCTURE [J].
BORCHMAN, D ;
LAMBA, OP ;
SALMASSI, S ;
LOU, M ;
YAPPERT, MC .
LIPIDS, 1992, 27 (04) :261-265
[8]  
Borchman D, 1998, INVEST OPHTH VIS SCI, V39, P1053
[9]  
Buege J A, 1978, Methods Enzymol, V52, P302
[10]   STUDIES ON PEROXIDATION OF ARACHIDONIC-ACID IN DIFFERENT LIPOSOMES BELOW AND ABOVE PHASE-TRANSITION TEMPERATURE [J].
CERVATO, G ;
VIANI, P ;
MASSERINI, M ;
DIIORIO, C ;
CESTARO, B .
CHEMISTRY AND PHYSICS OF LIPIDS, 1988, 49 (1-2) :135-139