Visualizing lipid structure and raft domains in living cells with two-photon microscopy

被引:443
作者
Gaus, K [1 ]
Gratton, E
Kable, EPW
Jones, AS
Gelissen, I
Kritharides, L
Jessup, W
机构
[1] Univ New S Wales, Ctr Vasc Res, Sydney, NSW 2052, Australia
[2] Prince Wales Hosp, Dept Haematol, Sydney, NSW 2052, Australia
[3] Univ Illinois, Fluorescence Dynam Lab, Urbana, IL 61801 USA
[4] Univ Sydney, Australian Key Ctr Microscopy & Microanal, Sydney, NSW 2006, Australia
[5] Univ Sydney, Concord Hosp, Dept Cardiol, Sydney, NSW 2139, Australia
关键词
membrane domains; macrophages;
D O I
10.1073/pnas.2534386100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
The lateral organization of cellular membranes is formed by the clustering of specific lipids, such as cholesterol and sphingolipids, into highly condensed domains (termed lipid rafts). Hence such domains are distinct from the remaining membrane by their lipid structure (liquid-ordered vs. -disordered domains). Here, we directly visualize membrane lipid structure of living cells by using two-photon microscopy. In macrophages, liquid-ordered domains are particularly enriched on membrane protrusions (filopodia), adhesion points and cell-cell contacts and cover 10-15% of the cell surface at 37degreesC. By deconvoluting the images, we demonstrate the existence of phase separation in vivo. We compare the properties of microscopically visible domains (< 1 mum(2)), with those of isolated detergent-resistant membranes and provide evidence that membrane coverage by lipid rafts and their fluidity are principally governed by cholesterol content, thereby providing strong support for the lipid raft hypothesis.
引用
收藏
页码:15554 / 15559
页数:6
相关论文
共 38 条
[1]
Two-photon fluorescence microscopy studies of bipolar tetraether giant liposomes from thermoacidophilic archaebacteria Sulfolobus acidocaldarius [J].
Bagatolli, L ;
Gratton, E ;
Khan, TK ;
Chong, PLG .
BIOPHYSICAL JOURNAL, 2000, 79 (01) :416-425
[2]
Two photon fluorescence microscopy of coexisting lipid domains in giant unilamellar vesicles of binary phospholipid mixtures [J].
Bagatolli, LA ;
Gratton, E .
BIOPHYSICAL JOURNAL, 2000, 78 (01) :290-305
[3]
Bagatolli LA, 1999, PHOTOCHEM PHOTOBIOL, V70, P557, DOI 10.1562/0031-8655(1999)070<0557:AMFTIO>2.3.CO
[4]
2
[5]
Two-photon fluorescence microscopy observation of shape changes at the phase transition in phospholipid giant unilamellar vesicles [J].
Bagatolli, LA ;
Gratton, E .
BIOPHYSICAL JOURNAL, 1999, 77 (04) :2090-2101
[6]
Bagatolli LA, 2003, METHOD ENZYMOL, V360, P481
[7]
Giant phospholipid vesicles: comparison among the whole lipid sample characteristics using different preparation methods - A two photon fluorescence microscopy study [J].
Bagatolli, LA ;
Parasassi, T ;
Gratton, E .
CHEMISTRY AND PHYSICS OF LIPIDS, 2000, 105 (02) :135-147
[8]
A correlation between lipid domain shape and binary phospholipid mixture composition in free standing bilayers: A two-photon fluorescence microscopy study [J].
Bagatolli, LA ;
Gratton, E .
BIOPHYSICAL JOURNAL, 2000, 79 (01) :434-447
[9]
Structure and function of sphingolipid- and cholesterol-rich membrane rafts [J].
Brown, DA ;
London, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (23) :17221-17224
[10]
Functions of lipid rafts in biological membranes [J].
Brown, DA ;
London, E .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1998, 14 :111-136