A crucial function of SGT1 and HSP90 in inflammasome activity links mammalian and plant innate immune responses.

Détails

ID Serval
serval:BIB_F48656689CBF
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
A crucial function of SGT1 and HSP90 in inflammasome activity links mammalian and plant innate immune responses.
Périodique
Nature Immunology
Auteur⸱e⸱s
Mayor A., Martinon F., De Smedt T., Pétrilli V., Tschopp J.
ISSN
1529-2908 (Print)
ISSN-L
1529-2908
Statut éditorial
Publié
Date de publication
2007
Volume
8
Numéro
5
Pages
497-503
Langue
anglais
Résumé
The family of mammalian Nod-like receptors (NLRs) consists of critical intracellular immune proteins structurally related to plant resistance proteins. The NLRs NALP3 and IPAF, for example, can each form a multiprotein proinflammatory complex called the 'inflammasome', and mutations in the gene encoding Nod2, another NLR, are positively associated with Crohn disease. Here we show that many NLRs interacted with the ubiquitin ligase-associated protein SGT1 and heat-shock protein 90 (HSP90), both of which have plant orthologs essential for R-protein responses. 'Knockdown' of SGT1 by small interfering RNA or chemical inhibition of HSP90 abrogated inflammasome activity, and inhibition of HSP90 blocked Nod2-mediated activation of the transcription factor NF-kappaB and reduced NALP3-mediated gout-like inflammation in mice. Our data demonstrate a similarity in one type of innate immunity in plants and mammals that is consistent with convergent evolution of a shared mechanism.
Mots-clé
Animals, Cell Cycle Proteins/physiology, Cells, Cultured, HSP90 Heat-Shock Proteins/chemistry, HSP90 Heat-Shock Proteins/physiology, Humans, Immunity, Innate, Inflammation/immunology, Mice, Mice, Inbred C57BL, Nod1 Signaling Adaptor Protein/genetics, Nod1 Signaling Adaptor Protein/metabolism, Plant Proteins/chemistry, Plant Proteins/genetics, Plants
Pubmed
Web of science
Création de la notice
24/01/2008 16:18
Dernière modification de la notice
20/08/2019 17:21
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