TLR activation of the transcription factor XBP1 regulates innate immune responses in macrophages.

Détails

ID Serval
serval:BIB_299B5C2A028A
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
TLR activation of the transcription factor XBP1 regulates innate immune responses in macrophages.
Périodique
Nature Immunology
Auteur(s)
Martinon F., Chen X., Lee A.H., Glimcher L.H.
ISSN
1529-2916 (Electronic)
ISSN-L
1529-2908
Statut éditorial
Publié
Date de publication
2010
Volume
11
Numéro
5
Pages
411-418
Langue
anglais
Résumé
Sensors of pathogens, such as Toll-like receptors (TLRs), detect microbes to activate transcriptional programs that orchestrate adaptive responses to specific insults. Here we report that TLR4 and TLR2 specifically activated the endoplasmic reticulum (ER) stress sensor kinase IRE1alpha and its downstream target, the transcription factor XBP1. Previously described ER-stress target genes of XBP1 were not induced by TLR signaling. Instead, TLR-activated XBP1 was required for optimal and sustained production of proinflammatory cytokines in macrophages. Consistent with that finding, activation of IRE1alpha by ER stress acted in synergy with TLR activation for cytokine production. Moreover, XBP1 deficiency resulted in a much greater bacterial burden in mice infected with the TLR2-activating human intracellular pathogen Francisella tularensis. Our findings identify an unsuspected critical function for XBP1 in mammalian host defenses.
Mots-clé
Animals, Cell Line, Cytokines/biosynthesis, Cytokines/genetics, DNA-Binding Proteins/genetics, DNA-Binding Proteins/immunology, Endoribonucleases/genetics, Endoribonucleases/immunology, Francisella tularensis/immunology, Francisella tularensis/pathogenicity, Immunity, Innate, Lipopeptides/pharmacology, Lipopolysaccharides/pharmacology, Macrophages/drug effects, Macrophages/immunology, Macrophages/</QualifierName> <QualifierName MajorTopicYN="N">, Membrane Glycoproteins/genetics, Membrane Glycoproteins/immunology, Mice, Mice, Inbred C3H, Mice, Knockout, Mice, Mutant Strains, Myeloid Differentiation Factor 88/genetics, Myeloid Differentiation Factor 88/metabolism, NADPH Oxidase/genetics, NADPH Oxidase/immunology, Protein Splicing/drug effects, Protein Splicing/genetics, Protein-Serine-Threonine Kinases/genetics, Protein-Serine-Threonine Kinases/immunology, RNA, Small Interfering/genetics, Signal Transduction/drug effects, Signal Transduction/genetics, Stress, Physiological/drug effects, Stress, Physiological/genetics, TNF Receptor-Associated Factor 6/genetics, TNF Receptor-Associated Factor 6/metabolism, Toll-Like Receptor 2/genetics, Toll-Like Receptor 2/immunology, Toll-Like Receptor 4/genetics, Toll-Like Receptor 4/immunology, Transcription Factor CHOP/biosynthesis, Transcription Factor CHOP/genetics, Transcription Factors/genetics, Transcription Factors/immunology, Transcriptional Activation/drug effects, Transcriptional Activation/immunology, Tularemia/genetics, Tularemia/immunology, Tunicamycin/pharmacology
Pubmed
Web of science
Création de la notice
21/02/2011 16:36
Dernière modification de la notice
20/08/2019 14:09
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