Source:http://linkedlifedata.com/resource/pubmed/id/21400499
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2011-3-28
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pubmed:abstractText |
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 ? chain-deficient mice; the CD4(-) subset coexpresses IL-22 and IL-17, and is common ? 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.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/CCR6 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Il2ra protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2 Receptor alpha Subunit,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-7 Receptor alpha Subunit,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukins,
http://linkedlifedata.com/resource/pubmed/chemical/Lipopolysaccharides,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, T-Cell...,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, CCR6,
http://linkedlifedata.com/resource/pubmed/chemical/interleukin-22
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1521-4141
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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pubmed:issnType |
Electronic
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pubmed:volume |
41
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1075-85
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pubmed:meshHeading |
pubmed-meshheading:21400499-Animals,
pubmed-meshheading:21400499-CD4-Positive T-Lymphocytes,
pubmed-meshheading:21400499-Immunity, Innate,
pubmed-meshheading:21400499-Inflammation,
pubmed-meshheading:21400499-Interleukin-2 Receptor alpha Subunit,
pubmed-meshheading:21400499-Interleukin-7 Receptor alpha Subunit,
pubmed-meshheading:21400499-Interleukins,
pubmed-meshheading:21400499-Lipopolysaccharides,
pubmed-meshheading:21400499-Mice,
pubmed-meshheading:21400499-Receptors, Antigen, T-Cell, gamma-delta,
pubmed-meshheading:21400499-Receptors, CCR6,
pubmed-meshheading:21400499-Spleen
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pubmed:year |
2011
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pubmed:articleTitle |
IL-22 is produced by ?C-independent CD25+ CCR6+ innate murine spleen cells upon inflammatory stimuli and contributes to LPS-induced lethality.
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pubmed:affiliation |
Ludwig Institute for Cancer Research, Brussels Branch, Belgium.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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