Source:http://linkedlifedata.com/resource/pubmed/id/19846871
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
|
pubmed:dateCreated |
2009-11-5
|
pubmed:abstractText |
Natural cytotoxicity receptors (including NKp30, NKp44, and NKp46 in humans and NKp46 in mice) are type I transmembrane proteins that signal NK cell activation via ITAM-containing adapter proteins in response to stress- and pathogen-induced ligands. Although murine NKp46 expression (encoded by Ncr1) was thought to be predominantly restricted to NK cells, the identification of distinct intestinal NKp46(+) cell subsets that express the transcription factor Rorc and produce IL-22 suggests a broader function for NKp46 that could involve intestinal homeostasis and immune defense. Using mice carrying a GFP-modified Ncr1 allele, we found normal numbers of gut CD3(-)GFP(+) cells with a similar cell surface phenotype and subset distribution in the absence of Ncr1. Splenic and intestinal CD3(-)NKp46(+) cell subsets showed distinct patterns of cytokine secretion (IFN-gamma, IL-22) following activation via NK1.1, NKp46, IL-12 plus IL-18, or IL-23. However, IL-22 production was sharply restricted to intestinal CD3(-)GFP(+) cells with the CD127(+)NK1.1(-) phenotype and could be induced in an Ncr1-independent fashion. Because NKp46 ligands can trigger immune activation in the context of infectious pathogens, we assessed the response of wild-type and Ncr-1-deficient Rag2(-/-) mice to the enteric pathogen Citrobacter rodentium. No differences in the survival or clinical score were observed in C. rodentium-infected Rag2(-/-) mice lacking Ncr1, indicating that NKp46 plays a redundant role in the differentiation of intestinal IL-22(+) cells that mediate innate defense against this pathogen. Our results provide further evidence for functional heterogeneity in intestinal NKp46(+) cells that contrast with splenic NK cells.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Ly,
http://linkedlifedata.com/resource/pubmed/chemical/Cytokines,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukins,
http://linkedlifedata.com/resource/pubmed/chemical/Natural Cytotoxicity Triggering...,
http://linkedlifedata.com/resource/pubmed/chemical/Ncr1 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Receptor Subfamily 1...,
http://linkedlifedata.com/resource/pubmed/chemical/Rag2 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Rorc protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/interleukin-22
|
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
1550-6606
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:day |
15
|
pubmed:volume |
183
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
6579-87
|
pubmed:meshHeading |
pubmed-meshheading:19846871-Animals,
pubmed-meshheading:19846871-Antigens, Ly,
pubmed-meshheading:19846871-Citrobacter rodentium,
pubmed-meshheading:19846871-Cytokines,
pubmed-meshheading:19846871-DNA-Binding Proteins,
pubmed-meshheading:19846871-Enterobacteriaceae Infections,
pubmed-meshheading:19846871-Immunity, Innate,
pubmed-meshheading:19846871-Interleukins,
pubmed-meshheading:19846871-Intestine, Small,
pubmed-meshheading:19846871-Killer Cells, Natural,
pubmed-meshheading:19846871-Lymphocyte Activation,
pubmed-meshheading:19846871-Mice,
pubmed-meshheading:19846871-Mice, Inbred C57BL,
pubmed-meshheading:19846871-Natural Cytotoxicity Triggering Receptor 1,
pubmed-meshheading:19846871-Nuclear Receptor Subfamily 1, Group F, Member 3,
pubmed-meshheading:19846871-Spleen
|
pubmed:year |
2009
|
pubmed:articleTitle |
The natural cytotoxicity receptor NKp46 is dispensable for IL-22-mediated innate intestinal immune defense against Citrobacter rodentium.
|
pubmed:affiliation |
Cytokines and Lymphoid Development Unit, Institut Pasteur, Paris, France.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|