Cholesterol is not crucial for the existence of microdomains in kidney brush-border membrane models

被引:67
作者
Milhiet, PE
Giocondi, MC
Le Grimellec, C
机构
[1] Univ Montpellier I, INSERM,CNRS UMR 5048, UMR554, CBS, F-34090 Montpellier, France
[2] Univ Paris 12, Lab CRRET, F-94000 Creteil, France
关键词
D O I
10.1074/jbc.C100654200
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
The external membrane leaflet plays a key role in the organization of the cell plasma membrane as a mosaic of ordered microdomains enriched in sphingolipids and cholesterol and of fluid domains. In this study, the thermotropic behavior and the topology of bilayers made of a phosphatidylcholine/sphingomyelin mixture, which mimicks the lipid composition of the external leaflet of renal brush-border membranes, were examined by differential scanning calorimetry and atomic force microscopy. In the absence of cholesterol, a broad phase separation process occurred where ordered gel phase domains of size varying from the mesoscopic to the microscopic scale, enriched in sphingomyelin, occupied half of the bilayer surface at room temperature. Increasing amounts of cholesterol progressively decreased the enthalpy of the transition and modified the topology of membranes domains up to a concentration of 33 mol % for which no membrane domains were detected. These results strongly suggest that, in membranes highly enriched in sphingolipids like renal and intestinal brush borders, there is a threshold close to the physiological concentration above which cholesterol acts as a suppressor rather than as a promoter of membrane domains. They also suggest that cholesterol depletion does not abolish the lateral heterogenity in brush-border membranes.
引用
收藏
页码:875 / 878
页数:4
相关论文
共 41 条
[1]   On the origin of sphingolipid/cholesterol-rich detergent-insoluble cell membranes: Physiological concentrations of cholesterol and sphingolipid induce formation of a detergent-insoluble, liquid-ordered lipid phase in model membranes [J].
Ahmed, SN ;
Brown, DA ;
London, E .
BIOCHEMISTRY, 1997, 36 (36) :10944-10953
[2]   Lipid monolayers: why use half a membrane to characterize protein-membrane interactions? [J].
Brockman, H .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 1999, 9 (04) :438-443
[3]   Structure and function of sphingolipid- and cholesterol-rich membrane rafts [J].
Brown, DA ;
London, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (23) :17221-17224
[4]   SORTING OF GPI-ANCHORED PROTEINS TO GLYCOLIPID-ENRICHED MEMBRANE SUBDOMAINS DURING TRANSPORT TO THE APICAL CELL-SURFACE [J].
BROWN, DA ;
ROSE, JK .
CELL, 1992, 68 (03) :533-544
[5]   COMPOSITION AND PHYSICAL-PROPERTIES OF LIPIDS FROM PLASMA-MEMBRANES OF DOG KIDNEY [J].
CARMEL, G ;
RODRIGUE, F ;
CARRIERE, S ;
LEGRIMELLEC, C .
BIOCHIMICA ET BIOPHYSICA ACTA, 1985, 818 (02) :149-157
[6]   PROTEIN-MEDIATED NET TRANSFER OF PHOSPHATIDYLINOSITOL IN MODEL SYSTEMS [J].
DEMEL, RA ;
KALSBEEK, R ;
WIRTZ, KWA ;
VANDEENEN, LLM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1977, 466 (01) :10-22
[7]  
DENKAMP JAF, 1981, NEW COMPREHENSIVE BI, V1, P83
[8]   Lipid rafts reconstituted in model membranes [J].
Dietrich, C ;
Bagatolli, LA ;
Volovyk, ZN ;
Thompson, NL ;
Levi, M ;
Jacobson, K ;
Gratton, E .
BIOPHYSICAL JOURNAL, 2001, 80 (03) :1417-1428
[9]   Nanometer-scale surface properties of mixed phospholipid monolayers and bilayers [J].
Dufrene, YF ;
Barger, WR ;
Green, JBD ;
Lee, GU .
LANGMUIR, 1997, 13 (18) :4779-4784
[10]   EFFECT OF CHOLESTEROL OXIDASE TREATMENT ON PHYSICAL STATE OF RENAL BRUSH-BORDER MEMBRANES - EVIDENCE FOR A CHOLESTEROL POOL INTERACTING WEAKLY WITH MEMBRANE-LIPIDS [J].
ELYANDOUZI, EH ;
LEGRIMELLEC, C .
BIOCHEMISTRY, 1993, 32 (08) :2047-2052