IL-22 is produced by γC-independent CD25+ ...
Type de document :
Article dans une revue scientifique: Article original
DOI :
PMID :
Titre :
IL-22 is produced by γC-independent CD25+ CCR6+ innate murine spleen cells upon inflammatory stimuli and contributes to LPS-induced lethality.
Auteur(s) :
Dumoutier, Laure [Auteur]
de Heusch, Magali [Auteur]
Orabona, Ciriana [Auteur]
Satoh-Takayama, Naoko [Auteur]
Immunité Innée - Innate Immunity
Eberl, Gerard [Auteur]
Développement des Tissus Lymphoïdes
Sirard, Jean-Claude [Auteur]
Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Di Santo, James [Auteur]
Immunité Innée - Innate Immunity
Renauld, Jean-Christophe [Auteur]
de Heusch, Magali [Auteur]
Orabona, Ciriana [Auteur]
Satoh-Takayama, Naoko [Auteur]
Immunité Innée - Innate Immunity
Eberl, Gerard [Auteur]
Développement des Tissus Lymphoïdes
Sirard, Jean-Claude [Auteur]

Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Di Santo, James [Auteur]
Immunité Innée - Innate Immunity
Renauld, Jean-Christophe [Auteur]
Titre de la revue :
European Journal of Immunology
Pagination :
1075-85
Éditeur :
Wiley-VCH Verlag
Date de publication :
2011-04
ISSN :
0014-2980
Discipline(s) HAL :
Sciences du Vivant [q-bio]/Immunologie
Résumé en anglais : [en]
IL-22 is a Th17 cytokine that plays a key role in immune responses against extracellular bacteria. In mucosal lymphoid tissues, IL-22 production is mainly due to an IL-23-responsive NK-like cell subset that shares some ...
Lire la suite >IL-22 is a Th17 cytokine that plays a key role in immune responses against extracellular bacteria. In mucosal lymphoid tissues, IL-22 production is mainly due to an IL-23-responsive NK-like cell subset that shares some markers with lymphoid tissue inducer (LTi) cells. Here, we identified a new spleen cell population responsible for IL-22 production upon either in vitro stimulation by anti-CD3 antibodies or in vivo stimulation by lipopolysaccharide (LPS) via IL-2- and an IL-23-dependent mechanisms, respectively. These cells represent 1% of spleen cells from recombination activating gene (Rag2)-deficient mice, and correspond to a discrete innate lymphoid cell population expressing CD25, CCR6 and IL-7R. This population comprises 60-70% CD4(+) cells, which produce IL-22, and are still present in common γ chain-deficient mice; the CD4(-) subset coexpresses IL-22 and IL-17, and is common γ chain-dependent. The importance of IL-22 production for the LPS-triggered response is highlighted by the fact that IL-22-deficient mice are more resistant to LPS-induced mortality.Lire moins >
Lire la suite >IL-22 is a Th17 cytokine that plays a key role in immune responses against extracellular bacteria. In mucosal lymphoid tissues, IL-22 production is mainly due to an IL-23-responsive NK-like cell subset that shares some markers with lymphoid tissue inducer (LTi) cells. Here, we identified a new spleen cell population responsible for IL-22 production upon either in vitro stimulation by anti-CD3 antibodies or in vivo stimulation by lipopolysaccharide (LPS) via IL-2- and an IL-23-dependent mechanisms, respectively. These cells represent 1% of spleen cells from recombination activating gene (Rag2)-deficient mice, and correspond to a discrete innate lymphoid cell population expressing CD25, CCR6 and IL-7R. This population comprises 60-70% CD4(+) cells, which produce IL-22, and are still present in common γ chain-deficient mice; the CD4(-) subset coexpresses IL-22 and IL-17, and is common γ chain-dependent. The importance of IL-22 production for the LPS-triggered response is highlighted by the fact that IL-22-deficient mice are more resistant to LPS-induced mortality.Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Source :