Lipoteichoic acid from Staphylococcus aureus induces lung endothelial cell barrier dysfunction: role of reactive oxygen and nitrogen species.

Tunneled central venous catheters (TCVCs) are used for dialysis access in 82% of new hemodialysis patients and are rapidly colonized with Gram-positive organism (e.g. Staphylococcus aureus) biofilm, a source of recurrent infections and chronic inflammation. Lipoteichoic acid (LTA), a cell wall ribit...

Full description

Bibliographic Details
Main Authors: Amy Barton Pai, Heena Patel, Alexander J Prokopienko, Hiba Alsaffar, Nancy Gertzberg, Paul Neumann, Anjoli Punjabi, Arnold Johnson
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3499573?pdf=render
_version_ 1818538622035427328
author Amy Barton Pai
Heena Patel
Alexander J Prokopienko
Hiba Alsaffar
Nancy Gertzberg
Paul Neumann
Anjoli Punjabi
Arnold Johnson
author_facet Amy Barton Pai
Heena Patel
Alexander J Prokopienko
Hiba Alsaffar
Nancy Gertzberg
Paul Neumann
Anjoli Punjabi
Arnold Johnson
author_sort Amy Barton Pai
collection DOAJ
description Tunneled central venous catheters (TCVCs) are used for dialysis access in 82% of new hemodialysis patients and are rapidly colonized with Gram-positive organism (e.g. Staphylococcus aureus) biofilm, a source of recurrent infections and chronic inflammation. Lipoteichoic acid (LTA), a cell wall ribitol polymer from Gram-positive organisms, mediates inflammation through the Toll-like receptor 2 (TLR2). The effect of LTA on lung endothelial permeability is not known. We tested the hypothesis that LTA from Staphylococcus aureus induces alterations in the permeability of pulmonary microvessel endothelial monolayers (PMEM) that result from activation of TLR2 and are mediated by reactive oxygen/nitrogen species (RONS). The permeability of PMEM was assessed by the clearance rate of Evans blue-labeled albumin, the activation of the TLR2 pathway was assessed by Western blot, and the generation of RONS was measured by the fluorescence of oxidized dihydroethidium and a dichlorofluorescein derivative. Treatment with LTA or the TLR2 agonist Pam((3))CSK((4)) induced significant increases in albumin permeability, IκBα phosphorylation, IRAK1 degradation, RONS generation, and endothelial nitric oxide synthase (eNOS) activation (as measured by the p-eNOS(ser1177):p-eNOS(thr495) ratio). The effects on permeability and RONS were effectively prevented by co-administration of the superoxide scavenger Tiron, the peroxynitrite scavenger Urate, or the eNOS inhibitor L-NAME and these effects as well as eNOS activation were reduced or prevented by pretreatment with an IRAK1/4 inhibitor. The results indicate that the activation of TLR2 and the generation of ROS/RNS mediates LTA-induced barrier dysfunction in PMEM.
first_indexed 2024-12-11T21:31:20Z
format Article
id doaj.art-57ecddb1666f48febce17b481dc8e31e
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-12-11T21:31:20Z
publishDate 2012-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-57ecddb1666f48febce17b481dc8e31e2022-12-22T00:50:10ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01711e4920910.1371/journal.pone.0049209Lipoteichoic acid from Staphylococcus aureus induces lung endothelial cell barrier dysfunction: role of reactive oxygen and nitrogen species.Amy Barton PaiHeena PatelAlexander J ProkopienkoHiba AlsaffarNancy GertzbergPaul NeumannAnjoli PunjabiArnold JohnsonTunneled central venous catheters (TCVCs) are used for dialysis access in 82% of new hemodialysis patients and are rapidly colonized with Gram-positive organism (e.g. Staphylococcus aureus) biofilm, a source of recurrent infections and chronic inflammation. Lipoteichoic acid (LTA), a cell wall ribitol polymer from Gram-positive organisms, mediates inflammation through the Toll-like receptor 2 (TLR2). The effect of LTA on lung endothelial permeability is not known. We tested the hypothesis that LTA from Staphylococcus aureus induces alterations in the permeability of pulmonary microvessel endothelial monolayers (PMEM) that result from activation of TLR2 and are mediated by reactive oxygen/nitrogen species (RONS). The permeability of PMEM was assessed by the clearance rate of Evans blue-labeled albumin, the activation of the TLR2 pathway was assessed by Western blot, and the generation of RONS was measured by the fluorescence of oxidized dihydroethidium and a dichlorofluorescein derivative. Treatment with LTA or the TLR2 agonist Pam((3))CSK((4)) induced significant increases in albumin permeability, IκBα phosphorylation, IRAK1 degradation, RONS generation, and endothelial nitric oxide synthase (eNOS) activation (as measured by the p-eNOS(ser1177):p-eNOS(thr495) ratio). The effects on permeability and RONS were effectively prevented by co-administration of the superoxide scavenger Tiron, the peroxynitrite scavenger Urate, or the eNOS inhibitor L-NAME and these effects as well as eNOS activation were reduced or prevented by pretreatment with an IRAK1/4 inhibitor. The results indicate that the activation of TLR2 and the generation of ROS/RNS mediates LTA-induced barrier dysfunction in PMEM.http://europepmc.org/articles/PMC3499573?pdf=render
spellingShingle Amy Barton Pai
Heena Patel
Alexander J Prokopienko
Hiba Alsaffar
Nancy Gertzberg
Paul Neumann
Anjoli Punjabi
Arnold Johnson
Lipoteichoic acid from Staphylococcus aureus induces lung endothelial cell barrier dysfunction: role of reactive oxygen and nitrogen species.
PLoS ONE
title Lipoteichoic acid from Staphylococcus aureus induces lung endothelial cell barrier dysfunction: role of reactive oxygen and nitrogen species.
title_full Lipoteichoic acid from Staphylococcus aureus induces lung endothelial cell barrier dysfunction: role of reactive oxygen and nitrogen species.
title_fullStr Lipoteichoic acid from Staphylococcus aureus induces lung endothelial cell barrier dysfunction: role of reactive oxygen and nitrogen species.
title_full_unstemmed Lipoteichoic acid from Staphylococcus aureus induces lung endothelial cell barrier dysfunction: role of reactive oxygen and nitrogen species.
title_short Lipoteichoic acid from Staphylococcus aureus induces lung endothelial cell barrier dysfunction: role of reactive oxygen and nitrogen species.
title_sort lipoteichoic acid from staphylococcus aureus induces lung endothelial cell barrier dysfunction role of reactive oxygen and nitrogen species
url http://europepmc.org/articles/PMC3499573?pdf=render
work_keys_str_mv AT amybartonpai lipoteichoicacidfromstaphylococcusaureusinduceslungendothelialcellbarrierdysfunctionroleofreactiveoxygenandnitrogenspecies
AT heenapatel lipoteichoicacidfromstaphylococcusaureusinduceslungendothelialcellbarrierdysfunctionroleofreactiveoxygenandnitrogenspecies
AT alexanderjprokopienko lipoteichoicacidfromstaphylococcusaureusinduceslungendothelialcellbarrierdysfunctionroleofreactiveoxygenandnitrogenspecies
AT hibaalsaffar lipoteichoicacidfromstaphylococcusaureusinduceslungendothelialcellbarrierdysfunctionroleofreactiveoxygenandnitrogenspecies
AT nancygertzberg lipoteichoicacidfromstaphylococcusaureusinduceslungendothelialcellbarrierdysfunctionroleofreactiveoxygenandnitrogenspecies
AT paulneumann lipoteichoicacidfromstaphylococcusaureusinduceslungendothelialcellbarrierdysfunctionroleofreactiveoxygenandnitrogenspecies
AT anjolipunjabi lipoteichoicacidfromstaphylococcusaureusinduceslungendothelialcellbarrierdysfunctionroleofreactiveoxygenandnitrogenspecies
AT arnoldjohnson lipoteichoicacidfromstaphylococcusaureusinduceslungendothelialcellbarrierdysfunctionroleofreactiveoxygenandnitrogenspecies