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Cholesterol interactions with phospholipids in membranes
Abstract
Mammalian cell membranes are composed of a complex array of glycerophospholipids and sphingolipids that vary in head-group and acyl-chain composition. In a given cell type, membrane phospholipids may amount to more than a thousand molecular species. The complexity of phospholipid and sphingolipid structures is most likely a consequence of their diverse roles in membrane dynamics, protein regulation, signal transduction and secretion. This review is mainly focused on two of the major classes of membrane phospholipids in eukaryotic organisms, sphingomyelins and phosphatidylcholines. These phospholipid classes constitute more than 50% of membrane phospholipids. Cholesterol is most likely to associate with these lipids in the membranes of the cells. We discuss the synthesis and distribution in the cell of these lipids, how they are believed to interact with each other, and what cellular consequences such interactions may have. We also include a discussion about findings in the recent literature regarding cholesterol/phospholipid interactions in model membrane systems. Finally, we look at the recent trends in computer and molecular dynamics simulations regarding phospholipid and cholesterol/phospholipid behavior in bilayer membranes.
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The majority of plasma membrane cholesterol forms complexes with other membrane lipids, including sphingomyelin and phospholipids, and is sequestered and inaccessible for intracellular transport.
“Normally, the majority of PM cholesterol forms complexes with other membrane lipids, including sphingomyelin and phospholipids, and is therefore sequestered and inaccessible for intracellular transport (also known as “chemically inactive”)”
From Molecular basis of accessible plasma membrane cholesterol recognition by the GRAM domain of GRAMD1b (2021) · cites this paper as Ohvo‐Rekila et al, 2002
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Metadata
- Authors
- Ohvo-Rekilä, H.
- Venue
- Progress in Lipid Research
- Publisher
- Elsevier BV
- Published
- 2002-01
- Volume
- 41
- Issue
- 1
- Pages
- 66-97
- ISSN
- 0163-7827
- Cited by
- 1,003
- References
- 0
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