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Interaction Between VLDL and Phosphatidylcholine Liposomes Generates New γ-LpE-like Particles

One of the subfractions of HDL involved in reverse cholesterol transport is γ-LpE. It has been assumed that, like preβ-LpAI, it can be generated during the interaction between phosphatidylcholine liposomes and lipoproteins and can contribute to more efficient cholesterol efflux after the introductio...

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Autores principales: Ćwiklińska, Agnieszka, Kortas-Stempak, Barbara, Gliwińska, Anna, Pacanis, Anastasis, Kuchta, Agnieszka, Wróblewska, Małgorzata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902082/
https://www.ncbi.nlm.nih.gov/pubmed/24234844
http://dx.doi.org/10.1007/s11745-013-3861-8
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author Ćwiklińska, Agnieszka
Kortas-Stempak, Barbara
Gliwińska, Anna
Pacanis, Anastasis
Kuchta, Agnieszka
Wróblewska, Małgorzata
author_facet Ćwiklińska, Agnieszka
Kortas-Stempak, Barbara
Gliwińska, Anna
Pacanis, Anastasis
Kuchta, Agnieszka
Wróblewska, Małgorzata
author_sort Ćwiklińska, Agnieszka
collection PubMed
description One of the subfractions of HDL involved in reverse cholesterol transport is γ-LpE. It has been assumed that, like preβ-LpAI, it can be generated during the interaction between phosphatidylcholine liposomes and lipoproteins and can contribute to more efficient cholesterol efflux after the introduction of liposomes to plasma. However, there has been no evidence concerning what the sources of these particles in plasma might be. Here, we determined whether the interaction of phosphatidylcholine liposomes with VLDL and the subsequent conversions of particles could be a source of new γ-LpE particles. We found that the interaction between liposomes and VLDL affected its lipid and protein composition. The content of phospholipids increased (~96 %) while the content of free cholesterol and apolipoprotein E decreased in VLDL during the reaction with liposomes (~100 and ~24 %, respectively). New particles which did not contain apolipoprotein B were generated. Heterogeneous HDL-sized populations of particles were generated, containing phospholipids and apolipoprotein E as the sole apolipoprotein, with densities from 1.063 to 1.21 g/ml, either with γ-mobility on agarose gel and Stokes diameters from 8.58 to 22.07 nm or with preβ-mobility and Stokes diameters from 9.9 to 21.08 nm. The obtained results contribute to the understanding of changes in lipoproteins under the influence of phosphatidylcholine liposomes, showing the formation of new (γ-LpE)-like and (preβ-LpE)-like particles, similar in mobility and size to plasma HDL-LpE. These newly generated particles can claim a share of the antiatherogenic effects of liposomes, observed in studies both in vitro and in vivo.
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spelling pubmed-39020822014-01-30 Interaction Between VLDL and Phosphatidylcholine Liposomes Generates New γ-LpE-like Particles Ćwiklińska, Agnieszka Kortas-Stempak, Barbara Gliwińska, Anna Pacanis, Anastasis Kuchta, Agnieszka Wróblewska, Małgorzata Lipids Original Article One of the subfractions of HDL involved in reverse cholesterol transport is γ-LpE. It has been assumed that, like preβ-LpAI, it can be generated during the interaction between phosphatidylcholine liposomes and lipoproteins and can contribute to more efficient cholesterol efflux after the introduction of liposomes to plasma. However, there has been no evidence concerning what the sources of these particles in plasma might be. Here, we determined whether the interaction of phosphatidylcholine liposomes with VLDL and the subsequent conversions of particles could be a source of new γ-LpE particles. We found that the interaction between liposomes and VLDL affected its lipid and protein composition. The content of phospholipids increased (~96 %) while the content of free cholesterol and apolipoprotein E decreased in VLDL during the reaction with liposomes (~100 and ~24 %, respectively). New particles which did not contain apolipoprotein B were generated. Heterogeneous HDL-sized populations of particles were generated, containing phospholipids and apolipoprotein E as the sole apolipoprotein, with densities from 1.063 to 1.21 g/ml, either with γ-mobility on agarose gel and Stokes diameters from 8.58 to 22.07 nm or with preβ-mobility and Stokes diameters from 9.9 to 21.08 nm. The obtained results contribute to the understanding of changes in lipoproteins under the influence of phosphatidylcholine liposomes, showing the formation of new (γ-LpE)-like and (preβ-LpE)-like particles, similar in mobility and size to plasma HDL-LpE. These newly generated particles can claim a share of the antiatherogenic effects of liposomes, observed in studies both in vitro and in vivo. Springer Berlin Heidelberg 2013-11-15 2014 /pmc/articles/PMC3902082/ /pubmed/24234844 http://dx.doi.org/10.1007/s11745-013-3861-8 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Ćwiklińska, Agnieszka
Kortas-Stempak, Barbara
Gliwińska, Anna
Pacanis, Anastasis
Kuchta, Agnieszka
Wróblewska, Małgorzata
Interaction Between VLDL and Phosphatidylcholine Liposomes Generates New γ-LpE-like Particles
title Interaction Between VLDL and Phosphatidylcholine Liposomes Generates New γ-LpE-like Particles
title_full Interaction Between VLDL and Phosphatidylcholine Liposomes Generates New γ-LpE-like Particles
title_fullStr Interaction Between VLDL and Phosphatidylcholine Liposomes Generates New γ-LpE-like Particles
title_full_unstemmed Interaction Between VLDL and Phosphatidylcholine Liposomes Generates New γ-LpE-like Particles
title_short Interaction Between VLDL and Phosphatidylcholine Liposomes Generates New γ-LpE-like Particles
title_sort interaction between vldl and phosphatidylcholine liposomes generates new γ-lpe-like particles
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902082/
https://www.ncbi.nlm.nih.gov/pubmed/24234844
http://dx.doi.org/10.1007/s11745-013-3861-8
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