Differential expression of NLRP3 among hematopoietic cells.

Détails

ID Serval
serval:BIB_C1B989E17195
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Differential expression of NLRP3 among hematopoietic cells.
Périodique
Journal of Immunology
Auteur(s)
Guarda G., Zenger M., Yazdi A.S., Schroder K., Ferrero I., Menu P., Tardivel A., Mattmann C., Tschopp J.
ISSN
1550-6606 (Electronic)
ISSN-L
0022-1767
Statut éditorial
Publié
Date de publication
2011
Volume
186
Numéro
4
Pages
2529-2534
Langue
anglais
Résumé
Although the importance of the NOD-like receptor family, pyrin domain containing 3 (NLRP3) inflammasome in health and disease is well appreciated, a precise characterization of NLRP3 expression is yet undetermined. To this purpose, we generated a knock-in mouse in which the Nlrp3 coding sequence was substituted for the GFP (enhanced GFP [egfp]) gene. In this way, the expression of eGFP is driven by the endogenous regulatory elements of the Nlrp3 gene. In this study, we show that eGFP expression indeed mirrors that of NLRP3. Interestingly, splenic neutrophils, macrophages, and, in particular, monocytes and conventional dendritic cells showed robust eGFP fluorescence, whereas lymphoid subsets, eosinophils, and plasmacytoid dendritic cells showed negligible eGFP levels. NLRP3 expression was highly inducible in macrophages, both by MyD88- and Trif-dependent pathways. In vivo, when mice were challenged with diverse inflammatory stimuli, differences in both the number of eGFP-expressing cells and fluorescence intensity were observed in the draining lymph node. Thus, NLRP3 levels at the site of adaptive response initiation are controlled by recruitment of NLRP3-expressing cells and by NLRP3 induction.
Mots-clé
Animals, Bone Marrow Cells/immunology, Bone Marrow Cells/metabolism, Carrier Proteins/biosynthesis, Carrier Proteins/genetics, Cell Movement/genetics, Cell Movement/immunology, Cells, Cultured, Dendritic Cells/immunology, Dendritic Cells/metabolism, Fluorescent Dyes/metabolism, Gene Expression Regulation/immunology, Gene Knock-In Techniques, Genes, Reporter/immunology, Green Fluorescent Proteins/biosynthesis, Green Fluorescent Proteins/deficiency, Hematopoietic Stem Cells/immunology, Hematopoietic Stem Cells/metabolism, Inflammation Mediators/metabolism, Mice, Mice, Inbred C57BL, Mice, Knockout, Monocytes/immunology, Monocytes/metabolism, Myeloid Cells/immunology, Myeloid Cells/metabolism, Spleen/immunology, Spleen/metabolism
Pubmed
Web of science
Création de la notice
02/09/2011 9:00
Dernière modification de la notice
20/08/2019 15:36
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