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

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 leukemi...

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Autores principales: Kakuda, Shinako, Suresh, Pavana, Li, Guangtao, London, Erwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8953672/
https://www.ncbi.nlm.nih.gov/pubmed/34843684
http://dx.doi.org/10.1016/j.jlr.2021.100155
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author Kakuda, Shinako
Suresh, Pavana
Li, Guangtao
London, Erwin
author_facet Kakuda, Shinako
Suresh, Pavana
Li, Guangtao
London, Erwin
author_sort Kakuda, Shinako
collection PubMed
description 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 ∼37°C, whereas ordered domains in symmetric vesicles formed from the extracted PMV lipids were stable up to 55°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.
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spelling pubmed-89536722022-03-31 Loss of plasma membrane lipid asymmetry can induce ordered domain (raft) formation Kakuda, Shinako Suresh, Pavana Li, Guangtao London, Erwin J Lipid Res Research Article 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 ∼37°C, whereas ordered domains in symmetric vesicles formed from the extracted PMV lipids were stable up to 55°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. American Society for Biochemistry and Molecular Biology 2021-11-26 /pmc/articles/PMC8953672/ /pubmed/34843684 http://dx.doi.org/10.1016/j.jlr.2021.100155 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Kakuda, Shinako
Suresh, Pavana
Li, Guangtao
London, Erwin
Loss of plasma membrane lipid asymmetry can induce ordered domain (raft) formation
title Loss of plasma membrane lipid asymmetry can induce ordered domain (raft) formation
title_full Loss of plasma membrane lipid asymmetry can induce ordered domain (raft) formation
title_fullStr Loss of plasma membrane lipid asymmetry can induce ordered domain (raft) formation
title_full_unstemmed Loss of plasma membrane lipid asymmetry can induce ordered domain (raft) formation
title_short Loss of plasma membrane lipid asymmetry can induce ordered domain (raft) formation
title_sort loss of plasma membrane lipid asymmetry can induce ordered domain (raft) formation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8953672/
https://www.ncbi.nlm.nih.gov/pubmed/34843684
http://dx.doi.org/10.1016/j.jlr.2021.100155
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