Meningococcal outer membrane protein NhhA triggers apoptosis in macrophages.

Phagocytotic cells play a fundamental role in the defense against bacterial pathogens. One mechanism whereby bacteria evade phagocytosis is to produce factors that trigger apoptosis. Here we identify for the first time a meningococcal protein capable of inducing macrophage apoptosis. The conserved m...

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Main Authors: Mikael Sjölinder, Georg Altenbacher, Matthias Hagner, Wei Sun, Sophia Schedin-Weiss, Hong Sjölinder
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3251587?pdf=render
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spelling doaj-5b6916ce164342428c4af224d3927fc82020-11-25T02:50:06ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0171e2958610.1371/journal.pone.0029586Meningococcal outer membrane protein NhhA triggers apoptosis in macrophages.Mikael SjölinderGeorg AltenbacherMatthias HagnerWei SunSophia Schedin-WeissHong SjölinderPhagocytotic cells play a fundamental role in the defense against bacterial pathogens. One mechanism whereby bacteria evade phagocytosis is to produce factors that trigger apoptosis. Here we identify for the first time a meningococcal protein capable of inducing macrophage apoptosis. The conserved meningococcal outer membrane protein NhhA (Neisseria hia/hsf homologue A, also known as Hsf) mediates bacterial adhesion and interacts with extracellular matrix components heparan sulphate and laminin. Meningococci lacking NhhA fail to colonise nasal mucosa in a mouse model of meningococcal disease. We found that exposure of macrophages to NhhA resulted in a highly increased rate of apoptosis that proceeded through caspase activation. Exposure of macrophages to NhhA also led to iNOS induction and nitric oxide production. However, neither nitric oxide production nor TNF-α signaling was found to be a prerequisite for NhhA-induced apoptosis. Macrophages exposed to wildtype NhhA-expressing meningococci were also found to undergo apoptosis whereas NhhA-deficient meningococci had a markedly decreased capacity to induce macrophage apoptosis. These data provide new insights on the role of NhhA in meningococcal disease. NhhA-induced macrophage apoptosis could be a mechanism whereby meningococci evade immunoregulatory and phagocytotic actions of macrophages.http://europepmc.org/articles/PMC3251587?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Mikael Sjölinder
Georg Altenbacher
Matthias Hagner
Wei Sun
Sophia Schedin-Weiss
Hong Sjölinder
spellingShingle Mikael Sjölinder
Georg Altenbacher
Matthias Hagner
Wei Sun
Sophia Schedin-Weiss
Hong Sjölinder
Meningococcal outer membrane protein NhhA triggers apoptosis in macrophages.
PLoS ONE
author_facet Mikael Sjölinder
Georg Altenbacher
Matthias Hagner
Wei Sun
Sophia Schedin-Weiss
Hong Sjölinder
author_sort Mikael Sjölinder
title Meningococcal outer membrane protein NhhA triggers apoptosis in macrophages.
title_short Meningococcal outer membrane protein NhhA triggers apoptosis in macrophages.
title_full Meningococcal outer membrane protein NhhA triggers apoptosis in macrophages.
title_fullStr Meningococcal outer membrane protein NhhA triggers apoptosis in macrophages.
title_full_unstemmed Meningococcal outer membrane protein NhhA triggers apoptosis in macrophages.
title_sort meningococcal outer membrane protein nhha triggers apoptosis in macrophages.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Phagocytotic cells play a fundamental role in the defense against bacterial pathogens. One mechanism whereby bacteria evade phagocytosis is to produce factors that trigger apoptosis. Here we identify for the first time a meningococcal protein capable of inducing macrophage apoptosis. The conserved meningococcal outer membrane protein NhhA (Neisseria hia/hsf homologue A, also known as Hsf) mediates bacterial adhesion and interacts with extracellular matrix components heparan sulphate and laminin. Meningococci lacking NhhA fail to colonise nasal mucosa in a mouse model of meningococcal disease. We found that exposure of macrophages to NhhA resulted in a highly increased rate of apoptosis that proceeded through caspase activation. Exposure of macrophages to NhhA also led to iNOS induction and nitric oxide production. However, neither nitric oxide production nor TNF-α signaling was found to be a prerequisite for NhhA-induced apoptosis. Macrophages exposed to wildtype NhhA-expressing meningococci were also found to undergo apoptosis whereas NhhA-deficient meningococci had a markedly decreased capacity to induce macrophage apoptosis. These data provide new insights on the role of NhhA in meningococcal disease. NhhA-induced macrophage apoptosis could be a mechanism whereby meningococci evade immunoregulatory and phagocytotic actions of macrophages.
url http://europepmc.org/articles/PMC3251587?pdf=render
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AT weisun meningococcaloutermembraneproteinnhhatriggersapoptosisinmacrophages
AT sophiaschedinweiss meningococcaloutermembraneproteinnhhatriggersapoptosisinmacrophages
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