Effects of Differences in Lipid A Structure on TLR4 Pro-inflammatory Signaling and Inflammasome Activation

The vertebrate immune system exists in equilibrium with the microbial world. The innate immune system recognizes pathogen-associated molecular patterns via a family of Toll-like receptors that activate cells upon detection of potential pathogens. Because some microbes benefit their hosts, mobilizi...

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Main Authors: Paula M Chilton, Chelsea A Embry, Thomas C Mitchell
Format: Article
Language:English
Published: Frontiers Media S.A. 2012-06-01
Series:Frontiers in Immunology
Subjects:
LPS
Online Access:http://journal.frontiersin.org/Journal/10.3389/fimmu.2012.00154/full
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spelling doaj-a6720bd92499469f9c7af73f52e6b0102020-11-24T22:43:26ZengFrontiers Media S.A.Frontiers in Immunology1664-32242012-06-01310.3389/fimmu.2012.0015425810Effects of Differences in Lipid A Structure on TLR4 Pro-inflammatory Signaling and Inflammasome ActivationPaula M Chilton0Chelsea A Embry1Thomas C Mitchell2University of LouisvilleStetson UniversityUniversity of LouisvilleThe vertebrate immune system exists in equilibrium with the microbial world. The innate immune system recognizes pathogen-associated molecular patterns via a family of Toll-like receptors that activate cells upon detection of potential pathogens. Because some microbes benefit their hosts, mobilizing the appropriate response and then controlling that response is critical in the maintenance of health. TLR4 recognizes the various forms of lipid A produced by gram-negative bacteria. Depending on the structural forms of the eliciting lipid A molecule, TLR4 responses range from a highly inflammatory endotoxic response involving inflammasome and other pro-inflammatory mediators, to an inhibitory, protective response. Mounting the correct response against an offending microbe is key to maintaining health when exposed to various bacterial species. Further study of lipid A variants may pave the way to understanding how TLR4 responses are generally able to avoid chronic inflammatory damage.http://journal.frontiersin.org/Journal/10.3389/fimmu.2012.00154/fullNLRP3InflammasomeMonophosphoryl Lipid ALPSTLR4
collection DOAJ
language English
format Article
sources DOAJ
author Paula M Chilton
Chelsea A Embry
Thomas C Mitchell
spellingShingle Paula M Chilton
Chelsea A Embry
Thomas C Mitchell
Effects of Differences in Lipid A Structure on TLR4 Pro-inflammatory Signaling and Inflammasome Activation
Frontiers in Immunology
NLRP3
Inflammasome
Monophosphoryl Lipid A
LPS
TLR4
author_facet Paula M Chilton
Chelsea A Embry
Thomas C Mitchell
author_sort Paula M Chilton
title Effects of Differences in Lipid A Structure on TLR4 Pro-inflammatory Signaling and Inflammasome Activation
title_short Effects of Differences in Lipid A Structure on TLR4 Pro-inflammatory Signaling and Inflammasome Activation
title_full Effects of Differences in Lipid A Structure on TLR4 Pro-inflammatory Signaling and Inflammasome Activation
title_fullStr Effects of Differences in Lipid A Structure on TLR4 Pro-inflammatory Signaling and Inflammasome Activation
title_full_unstemmed Effects of Differences in Lipid A Structure on TLR4 Pro-inflammatory Signaling and Inflammasome Activation
title_sort effects of differences in lipid a structure on tlr4 pro-inflammatory signaling and inflammasome activation
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2012-06-01
description The vertebrate immune system exists in equilibrium with the microbial world. The innate immune system recognizes pathogen-associated molecular patterns via a family of Toll-like receptors that activate cells upon detection of potential pathogens. Because some microbes benefit their hosts, mobilizing the appropriate response and then controlling that response is critical in the maintenance of health. TLR4 recognizes the various forms of lipid A produced by gram-negative bacteria. Depending on the structural forms of the eliciting lipid A molecule, TLR4 responses range from a highly inflammatory endotoxic response involving inflammasome and other pro-inflammatory mediators, to an inhibitory, protective response. Mounting the correct response against an offending microbe is key to maintaining health when exposed to various bacterial species. Further study of lipid A variants may pave the way to understanding how TLR4 responses are generally able to avoid chronic inflammatory damage.
topic NLRP3
Inflammasome
Monophosphoryl Lipid A
LPS
TLR4
url http://journal.frontiersin.org/Journal/10.3389/fimmu.2012.00154/full
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