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Effect of lipid peroxidation on membrane permeability of cancer and normal cells subjected to oxidative stress
We performed molecular dynamics simulations to investigate the effect of lipid peroxidation products on the structural and dynamic properties of the cell membrane. Our simulations predict that the lipid order in a phospholipid bilayer, as a model system for the cell membrane, decreases upon addition...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5518669/ https://www.ncbi.nlm.nih.gov/pubmed/28791102 http://dx.doi.org/10.1039/c5sc02311d |
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author | Van der Paal, Jonas Neyts, Erik C. Verlackt, Christof C. W. Bogaerts, Annemie |
author_facet | Van der Paal, Jonas Neyts, Erik C. Verlackt, Christof C. W. Bogaerts, Annemie |
author_sort | Van der Paal, Jonas |
collection | PubMed |
description | We performed molecular dynamics simulations to investigate the effect of lipid peroxidation products on the structural and dynamic properties of the cell membrane. Our simulations predict that the lipid order in a phospholipid bilayer, as a model system for the cell membrane, decreases upon addition of lipid peroxidation products. Eventually, when all phospholipids are oxidized, pore formation can occur. This will allow reactive species, such as reactive oxygen and nitrogen species (RONS), to enter the cell and cause oxidative damage to intracellular macromolecules, such as DNA or proteins. On the other hand, upon increasing the cholesterol fraction of lipid bilayers, the cell membrane order increases, eventually reaching a certain threshold, from which cholesterol is able to protect the membrane against pore formation. This finding is crucial for cancer treatment by plasma technology, producing a large number of RONS, as well as for other cancer treatment methods that cause an increase in the concentration of extracellular RONS. Indeed, cancer cells contain less cholesterol than their healthy counterparts. Thus, they will be more vulnerable to the consequences of lipid peroxidation, eventually enabling the penetration of RONS into the interior of the cell, giving rise to oxidative stress, inducing pro-apoptotic factors. This provides, for the first time, molecular level insight why plasma can selectively treat cancer cells, while leaving their healthy counterparts undamaged, as is indeed experimentally demonstrated. |
format | Online Article Text |
id | pubmed-5518669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-55186692017-08-08 Effect of lipid peroxidation on membrane permeability of cancer and normal cells subjected to oxidative stress Van der Paal, Jonas Neyts, Erik C. Verlackt, Christof C. W. Bogaerts, Annemie Chem Sci Chemistry We performed molecular dynamics simulations to investigate the effect of lipid peroxidation products on the structural and dynamic properties of the cell membrane. Our simulations predict that the lipid order in a phospholipid bilayer, as a model system for the cell membrane, decreases upon addition of lipid peroxidation products. Eventually, when all phospholipids are oxidized, pore formation can occur. This will allow reactive species, such as reactive oxygen and nitrogen species (RONS), to enter the cell and cause oxidative damage to intracellular macromolecules, such as DNA or proteins. On the other hand, upon increasing the cholesterol fraction of lipid bilayers, the cell membrane order increases, eventually reaching a certain threshold, from which cholesterol is able to protect the membrane against pore formation. This finding is crucial for cancer treatment by plasma technology, producing a large number of RONS, as well as for other cancer treatment methods that cause an increase in the concentration of extracellular RONS. Indeed, cancer cells contain less cholesterol than their healthy counterparts. Thus, they will be more vulnerable to the consequences of lipid peroxidation, eventually enabling the penetration of RONS into the interior of the cell, giving rise to oxidative stress, inducing pro-apoptotic factors. This provides, for the first time, molecular level insight why plasma can selectively treat cancer cells, while leaving their healthy counterparts undamaged, as is indeed experimentally demonstrated. Royal Society of Chemistry 2016-01-01 2015-10-16 /pmc/articles/PMC5518669/ /pubmed/28791102 http://dx.doi.org/10.1039/c5sc02311d Text en This journal is © The Royal Society of Chemistry 2015 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Van der Paal, Jonas Neyts, Erik C. Verlackt, Christof C. W. Bogaerts, Annemie Effect of lipid peroxidation on membrane permeability of cancer and normal cells subjected to oxidative stress |
title | Effect of lipid peroxidation on membrane permeability of cancer and normal cells subjected to oxidative stress
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title_full | Effect of lipid peroxidation on membrane permeability of cancer and normal cells subjected to oxidative stress
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title_fullStr | Effect of lipid peroxidation on membrane permeability of cancer and normal cells subjected to oxidative stress
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title_full_unstemmed | Effect of lipid peroxidation on membrane permeability of cancer and normal cells subjected to oxidative stress
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title_short | Effect of lipid peroxidation on membrane permeability of cancer and normal cells subjected to oxidative stress
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title_sort | effect of lipid peroxidation on membrane permeability of cancer and normal cells subjected to oxidative stress |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5518669/ https://www.ncbi.nlm.nih.gov/pubmed/28791102 http://dx.doi.org/10.1039/c5sc02311d |
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