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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
1997-1-23
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pubmed:abstractText |
Mice genetically deficient in IL-7R(alpha) are highly lymphopenic in the peripheral lymphoid organs. The functional competence of T cells that have developed in the absence of an IL-7R signal was investigated. Three important observations were made using several in vitro activation regimens. First, stimulation of T cells from IL-7R -/- mice at limiting dilution with immobilized Abs to CD3, CD4 or CD8, and CD18 revealed a six- to sevenfold reduction in the frequency of clonogenic T cells compared with T cells from IL-7R +/+ mice. IL-7R -/- T cells were also significantly less responsive to alloantigen as well as to receptor-independent stimuli such as PMA and ionomycin. Furthermore, the average clone size of single IL-7R -/- T cells was 50% smaller than that of IL-7R +/+ T cells. These data suggest that the reduced clonogenicity was predominantly due to intrinsic deficiencies in the ability of IL-7R -/- T cells to proliferate upon stimulation. Second, analysis of the kinetics of cell growth of IL-7R -/- T cells revealed that a significant proportion of T cells failed to proliferate within the first 72 h of in vitro stimulation, with the majority undergoing programmed cell death. Third, both clonogenic IL-7 -/- T cells and IL-7R +/+ T cells showed a similar proliferative response in the presence of IL-2 and similar survival kinetics, indicating that a subpopulation of IL-7R -/- T cells is functionally mature. We propose that an absence of IL-7R signaling not only affects T cell development in the thymus, but also results in the accumulation of functionally inactive T cells in the periphery.
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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, CD,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD95,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, T-Cell,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin-7
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
157
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5315-23
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pubmed:dateRevised |
2003-11-14
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pubmed:meshHeading |
pubmed-meshheading:8955178-Animals,
pubmed-meshheading:8955178-Antigens, CD,
pubmed-meshheading:8955178-Antigens, CD95,
pubmed-meshheading:8955178-Apoptosis,
pubmed-meshheading:8955178-CD4-Positive T-Lymphocytes,
pubmed-meshheading:8955178-CD8-Positive T-Lymphocytes,
pubmed-meshheading:8955178-Cell Survival,
pubmed-meshheading:8955178-Cells, Cultured,
pubmed-meshheading:8955178-Interleukin-2,
pubmed-meshheading:8955178-Lymphocyte Activation,
pubmed-meshheading:8955178-Mice,
pubmed-meshheading:8955178-Mice, Knockout,
pubmed-meshheading:8955178-Receptors, Antigen, T-Cell,
pubmed-meshheading:8955178-Receptors, Interleukin,
pubmed-meshheading:8955178-Receptors, Interleukin-7,
pubmed-meshheading:8955178-Spleen,
pubmed-meshheading:8955178-Thymus Gland
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pubmed:year |
1996
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pubmed:articleTitle |
Impaired survival and proliferation in IL-7 receptor-deficient peripheral T cells.
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pubmed:affiliation |
Department of Cellular Immunology, Immunex Corporation, Seattle, WA 98101, USA.
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pubmed:publicationType |
Journal Article
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