Source:http://linkedlifedata.com/resource/pubmed/id/19234143
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
22
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pubmed:dateCreated |
2009-5-29
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pubmed:abstractText |
Surface density of CD27 and CD11b subdivides mouse natural killer (NK) cells into 4 subsets: CD11b(low)CD27(low), CD11b(low)CD27(high), CD11b(high)CD27(high), and CD11b(high)CD27(low). To determine the developmental relationship between these 4 subsets, we used several complementary approaches. First, we took advantage of NDE transgenic mice that express enhanced green fluorescent protein (EGFP) and diphtheria toxin receptor specifically in NK cells. Diphtheria toxin injection leads to a transient depletion of NK cells, allowing the monitoring of the phenotype of developing EGFP+ NK cells after diphtheria toxin injection. Second, we evaluated the overall proximity between NK-cell subsets based on their global gene profile. Third, we compared the proliferative capacity of NK-cell subsets at steady state or during replenishment of the NK-cell pool. Fourth, we performed adoptive transfers of EGFP+ NK cell subsets from NDE mice into unirradiated mice and followed the fate of transferred cells. The results of these various experiments collectively support a 4-stage model of NK-cell maturation CD11b(low)CD27(low) --> CD11b(low)CD27(high) --> CD11b(high)CD27(high) --> CD11b(high)CD27(low). This developmental program appears to be associated with a progressive acquisition of NK-cell effector functions.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD11b,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD27,
http://linkedlifedata.com/resource/pubmed/chemical/Diphtheria Toxin,
http://linkedlifedata.com/resource/pubmed/chemical/Green Fluorescent Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/enhanced green fluorescent protein
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
1528-0020
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
28
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pubmed:volume |
113
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5488-96
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pubmed:meshHeading |
pubmed-meshheading:19234143-Animals,
pubmed-meshheading:19234143-Antigens, CD11b,
pubmed-meshheading:19234143-Antigens, CD27,
pubmed-meshheading:19234143-Cell Differentiation,
pubmed-meshheading:19234143-Cells, Cultured,
pubmed-meshheading:19234143-Diphtheria Toxin,
pubmed-meshheading:19234143-Gene Expression Profiling,
pubmed-meshheading:19234143-Green Fluorescent Proteins,
pubmed-meshheading:19234143-Killer Cells, Natural,
pubmed-meshheading:19234143-Lymphocyte Activation,
pubmed-meshheading:19234143-Mice,
pubmed-meshheading:19234143-Mice, Inbred C57BL,
pubmed-meshheading:19234143-Mice, Transgenic,
pubmed-meshheading:19234143-Oligonucleotide Array Sequence Analysis,
pubmed-meshheading:19234143-Time Factors
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pubmed:year |
2009
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pubmed:articleTitle |
Maturation of mouse NK cells is a 4-stage developmental program.
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pubmed:affiliation |
Centre d'Immunologie de Marseille-Luminy, Université de la Méditerranée, Marseille, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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