2000
DOI: 10.1074/jbc.r000005200
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Structure and Function of Sphingolipid- and Cholesterol-rich Membrane Rafts

Abstract: It is well known that separate domains with different lipid compositions can exist in liposomes containing mixtures of different phospholipids. The question of whether cellular membranes contain similar lipid domains has intrigued workers for many years. One type of domain, sphingolipid and cholesterol-based structures called membrane rafts, has received much attention in the last few years. We will review the evidence that rafts exist in cells and focus on their structure, or the organization of raft lipids a… Show more

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Cited by 2,201 publications
(1,822 citation statements)
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References 67 publications
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“…Successful application of the fluorescent DHE to investigation of the function and organization of sterols in membranes, especially lipid raft/ caveolae microdomains of living cells, requires the use of highly purified DHE. This is due to the fact that lipid rafts/caveolae are highly sensitive not only to cholesterol content (58,60,82,84,85,87,88), but also to sterol structure (89), and sterol oxidation. The present review yielded new insights into this problem and potential applications of DHE imaging in living cells.…”
Section: Summary and Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Successful application of the fluorescent DHE to investigation of the function and organization of sterols in membranes, especially lipid raft/ caveolae microdomains of living cells, requires the use of highly purified DHE. This is due to the fact that lipid rafts/caveolae are highly sensitive not only to cholesterol content (58,60,82,84,85,87,88), but also to sterol structure (89), and sterol oxidation. The present review yielded new insights into this problem and potential applications of DHE imaging in living cells.…”
Section: Summary and Discussionmentioning
confidence: 99%
“…Because of the tremendous interest of biologists and membraneologists in cholesterol-rich microdomains (also called lipid rafts or caveolae) over the past 15 years (rev. in (54)(55)(56)(57)(58)(59)(60)(61)(62)(63), DHE has emerged as a popular, potentially less perturbing fluorescent sterol probe since it does not contain additional bulky fluorescent groups added to the sterol structure. Although this ultraviolet (UV) light absorbing and fluorescent sterol (i.e.…”
Section: Advent Of Fluorescent Sterolsmentioning
confidence: 99%
“…Nevertheless, evidence for lipid domain formation has also been obtained in cells by monitoring the lateral movement of transmembrane proteins or the partition of fluorescent membrane probes [18][19][20] . The entities visualized by these techniques, which are generally thought to correspond to the detergent-resistant 'lipid rafts' that are isolated from tissue extracts [21][22][23] , may regulate cell function by facilitating selective protein-protein interactions within the plasma membrane 21 . In neurons and glia, it has been proposed that they may be implicated in stabilizing clusters of neurotransmitter receptors with proteins involved in intracellular signalling and the promotion of clathrinindependent endocytosis, and influence the activity and localization of neurotransmitter transporters 4,22 .…”
Section: Liposomementioning
confidence: 99%
“…The fluidic nature of rafts and raft-associated proteins are depicted in Figure 3B. The figure shows how clustering of proteins which have a high affinity for lipid rafts could cause either small rafts containing the protein to coalesce into larger rafts (I) or increase the overall affinity of the protein cluster enough to recruit it to rafts (II) (Brown and London, 2000). Once understood as playing a part in cellular mechanisms such as inter-cellular trafficking of lipids and lipid-anchored proteins, rafts are now considered essential components of physiological functions such as cell adhesion, cell sorting, membrane traffic and as docking sites for cellular signaling (Chauhan, 2003;Hanzal-Bayer and Hancock, 2007).…”
Section: Lipid Raftmentioning
confidence: 99%
“…Amyloid precursor protein (APP) is a transmembrane glycoprotein ( 100-130 kDa) expressed in many tissues and Clustering of proteins which have a high affinity for lipid rafts could cause either small rafts containing the protein to coalesce into larger rafts (I) or increase the overall affinity of the protein cluster enough to recruit it to rafts (II) (B) (Adapted from Brown and London, 2000).…”
Section: Alzheimer's Amyloidogenic Membrane-associated Proteinsmentioning
confidence: 99%