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Oxysterols Protect Epithelial Cells Against Pore-Forming Toxins

Many species of bacteria produce toxins such as cholesterol-dependent cytolysins that form pores in cell membranes. Membrane pores facilitate infection by releasing nutrients, delivering virulence factors, and causing lytic cell damage - cytolysis. Oxysterols are oxidized forms of cholesterol that r...

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Autores principales: Ormsby, Thomas J. R., Owens, Sian E., Clement, Liam, Mills, Tom J., Cronin, James G., Bromfield, John J., Sheldon, Iain Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825411/
https://www.ncbi.nlm.nih.gov/pubmed/35154132
http://dx.doi.org/10.3389/fimmu.2022.815775
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author Ormsby, Thomas J. R.
Owens, Sian E.
Clement, Liam
Mills, Tom J.
Cronin, James G.
Bromfield, John J.
Sheldon, Iain Martin
author_facet Ormsby, Thomas J. R.
Owens, Sian E.
Clement, Liam
Mills, Tom J.
Cronin, James G.
Bromfield, John J.
Sheldon, Iain Martin
author_sort Ormsby, Thomas J. R.
collection PubMed
description Many species of bacteria produce toxins such as cholesterol-dependent cytolysins that form pores in cell membranes. Membrane pores facilitate infection by releasing nutrients, delivering virulence factors, and causing lytic cell damage - cytolysis. Oxysterols are oxidized forms of cholesterol that regulate cellular cholesterol and alter immune responses to bacteria. Whether oxysterols also influence the protection of cells against pore-forming toxins is unresolved. Here we tested the hypothesis that oxysterols stimulate the intrinsic protection of epithelial cells against damage caused by cholesterol-dependent cytolysins. We treated epithelial cells with oxysterols and then challenged them with the cholesterol-dependent cytolysin, pyolysin. Treating HeLa cells with 27-hydroxycholesterol, 25-hydroxycholesterol, 7α-hydroxycholesterol, or 7β-hydroxycholesterol reduced pyolysin-induced leakage of lactate dehydrogenase and reduced pyolysin-induced cytolysis. Specifically, treatment with 10 ng/ml 27-hydroxycholesterol for 24 h reduced pyolysin-induced lactate dehydrogenase leakage by 88%, and reduced cytolysis from 74% to 1%. Treating HeLa cells with 27-hydroxycholesterol also reduced pyolysin-induced leakage of potassium ions, prevented mitogen-activated protein kinase cell stress responses, and limited alterations in the cytoskeleton. Furthermore, 27-hydroxycholesterol reduced pyolysin-induced damage in lung and liver epithelial cells, and protected against the cytolysins streptolysin O and Staphylococcus aureus α-hemolysin. Although oxysterols regulate cellular cholesterol by activating liver X receptors, cytoprotection did not depend on liver X receptors or changes in total cellular cholesterol. However, oxysterol cytoprotection was partially dependent on acyl-CoA:cholesterol acyltransferase (ACAT) reducing accessible cholesterol in cell membranes. Collectively, these findings imply that oxysterols stimulate the intrinsic protection of epithelial cells against pore-forming toxins and may help protect tissues against pathogenic bacteria.
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spelling pubmed-88254112022-02-10 Oxysterols Protect Epithelial Cells Against Pore-Forming Toxins Ormsby, Thomas J. R. Owens, Sian E. Clement, Liam Mills, Tom J. Cronin, James G. Bromfield, John J. Sheldon, Iain Martin Front Immunol Immunology Many species of bacteria produce toxins such as cholesterol-dependent cytolysins that form pores in cell membranes. Membrane pores facilitate infection by releasing nutrients, delivering virulence factors, and causing lytic cell damage - cytolysis. Oxysterols are oxidized forms of cholesterol that regulate cellular cholesterol and alter immune responses to bacteria. Whether oxysterols also influence the protection of cells against pore-forming toxins is unresolved. Here we tested the hypothesis that oxysterols stimulate the intrinsic protection of epithelial cells against damage caused by cholesterol-dependent cytolysins. We treated epithelial cells with oxysterols and then challenged them with the cholesterol-dependent cytolysin, pyolysin. Treating HeLa cells with 27-hydroxycholesterol, 25-hydroxycholesterol, 7α-hydroxycholesterol, or 7β-hydroxycholesterol reduced pyolysin-induced leakage of lactate dehydrogenase and reduced pyolysin-induced cytolysis. Specifically, treatment with 10 ng/ml 27-hydroxycholesterol for 24 h reduced pyolysin-induced lactate dehydrogenase leakage by 88%, and reduced cytolysis from 74% to 1%. Treating HeLa cells with 27-hydroxycholesterol also reduced pyolysin-induced leakage of potassium ions, prevented mitogen-activated protein kinase cell stress responses, and limited alterations in the cytoskeleton. Furthermore, 27-hydroxycholesterol reduced pyolysin-induced damage in lung and liver epithelial cells, and protected against the cytolysins streptolysin O and Staphylococcus aureus α-hemolysin. Although oxysterols regulate cellular cholesterol by activating liver X receptors, cytoprotection did not depend on liver X receptors or changes in total cellular cholesterol. However, oxysterol cytoprotection was partially dependent on acyl-CoA:cholesterol acyltransferase (ACAT) reducing accessible cholesterol in cell membranes. Collectively, these findings imply that oxysterols stimulate the intrinsic protection of epithelial cells against pore-forming toxins and may help protect tissues against pathogenic bacteria. Frontiers Media S.A. 2022-01-26 /pmc/articles/PMC8825411/ /pubmed/35154132 http://dx.doi.org/10.3389/fimmu.2022.815775 Text en Copyright © 2022 Ormsby, Owens, Clement, Mills, Cronin, Bromfield and Sheldon https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Ormsby, Thomas J. R.
Owens, Sian E.
Clement, Liam
Mills, Tom J.
Cronin, James G.
Bromfield, John J.
Sheldon, Iain Martin
Oxysterols Protect Epithelial Cells Against Pore-Forming Toxins
title Oxysterols Protect Epithelial Cells Against Pore-Forming Toxins
title_full Oxysterols Protect Epithelial Cells Against Pore-Forming Toxins
title_fullStr Oxysterols Protect Epithelial Cells Against Pore-Forming Toxins
title_full_unstemmed Oxysterols Protect Epithelial Cells Against Pore-Forming Toxins
title_short Oxysterols Protect Epithelial Cells Against Pore-Forming Toxins
title_sort oxysterols protect epithelial cells against pore-forming toxins
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825411/
https://www.ncbi.nlm.nih.gov/pubmed/35154132
http://dx.doi.org/10.3389/fimmu.2022.815775
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