Loss of plasma membrane lipid asymmetry can induce ordered domain (raft) formation

被引:11
|
作者
Kakuda, Shinako [1 ]
Suresh, Pavana [1 ]
Li, Guangtao [1 ]
London, Erwin [1 ]
机构
[1] SUNY Stony Brook, Dept Biochem & Cell Biol, Stony Brook, NY 11794 USA
关键词
lipid rafts; membrane domains; liquid ordered; fluorescence anisotropy; fluorescence resonance energy transfer; plasma membrane vesicles; leaflet asymmetry; N-ethyl maleimide; dithiothreitol; annexin; GPI-ANCHORED PROTEINS; RED-CELL MEMBRANE; CHOLESTEROL; VESICLES; PHOSPHOLIPIDS; RECONSTITUTION; NANODOMAINS; STABILITY; PROMOTES;
D O I
10.1016/j.jlr.2021.100155
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
In some cases, lipids in one leaflet of an asymmetric artificial lipid vesicle suppress the formation of ordered lipid domains ( rafts) in the opposing leaflet. Whether this occurs in natural membranes is unknown. Here, we investigated this issue using plasma membrane vesicles (PMVs) from rat leukemia RBL-2H3 cells. Membrane domain formation and order was assessed by fluorescence resonance energy transfer and fluorescence anisotropy. We found that ordered domains in PMVs prepared from cells by N-ethyl maleimide (NEM) treatment formed up to similar to 37 degrees C, whereas ordered domains in symmetric vesicles formed from the extracted PMV lipids were stable up to 55 degrees C, indicating the stability of ordered domains was substantially decreased in intact PMVs. This behavior paralleled lesser ordered domain stability in artificial asymmetric lipid vesicles relative to the corresponding symmetric vesicles, suggesting intact PMVs exhibit some degree of lipid asymmetry. This was supported by phosphatidylserine mislocalization on PMV outer leaflets as judged by annexin binding, which indicated NEM-induced PMVs are much more asymmetric than PMVs formed by dithiothreitol/paraformaldehyde treatment. Destroying asymmetry by reconstitution of PMVs using detergent dilution also showed stabilization of domain formation, even though membrane proteins remained associated with reconstituted vesicles. Similar domain stabilization was observed in artificial asymmetric lipid vesicles after destroying asymmetry via detergent reconstitution. Proteinase K digestion of proteins had little effect on domain stability in NEM PMVs. We conclude that loss of PMV lipid asymmetry can induce ordered domain formation. The dynamic control of lipid asymmetry in cells may regulate domain formation in plasma membranes.
引用
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页数:13
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