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rdf:type | |
lifeskim:mentions |
umls-concept:C0021756,
umls-concept:C0021761,
umls-concept:C0024501,
umls-concept:C0033414,
umls-concept:C0034790,
umls-concept:C0330390,
umls-concept:C0439097,
umls-concept:C0599739,
umls-concept:C0721534,
umls-concept:C0814999,
umls-concept:C1512656,
umls-concept:C1533691,
umls-concept:C1547348,
umls-concept:C1552644,
umls-concept:C1704689,
umls-concept:C1705241,
umls-concept:C1823153,
umls-concept:C2003941,
umls-concept:C2246476,
umls-concept:C2349976
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pubmed:issue |
9
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pubmed:dateCreated |
1989-11-30
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pubmed:abstractText |
IL-7 induced the proliferation of normal thymocytes and the effect was synergistically potentiated by a small dose of IL-2, which by itself hardly affected thymocyte proliferation. No synergism was observed between IL-7 and any one of the other lymphokines including IL-1, IL-3, and IL-4. The thymocyte culture stimulated with IL-7 and IL-2 consisted of single positive (CD4+CD8- and CD4-CD8+) and double negative (CD4-CD8-) populations, and double positive (CD4+CD8+) cells were completely deleted. Both single positive and double negative thymocytes expressed CD3, but only the former exhibited V beta 8 and V beta 6 in an expected proportion (approximately 30% in BALB/c mice) and the latter none at all. Immunoprecipitation of the cultured thymocytes by anti-TCR gamma antibody, on the other hand, revealed the presence of a TCR gamma chain. Taken together, these results indicated that the thymocyte cultured with IL-7 and IL-2 consisted of mature T cells bearing alpha beta or gamma delta TCR. Experiments using preselected thymocyte subpopulations indicated that double negative cells responded to both IL-7 and IL-2 with positive synergism when combined, while thymocytes enriched for single positive cells preferentially responded to IL-7 with little response to IL-2 and no detectable synergism. Double positive thymocytes showed no proliferation in response to IL-7 and IL-2. In contrast to single positive thymocytes, splenic T cells hardly responded to IL-7, although significant proliferation was induced in the presence of a low dose of IL-2. Thymocytes cultured with IL-7 and IL-2 showed little nonspecific cytotoxic activity, but responded to Con A or alloantigen, whereas those stimulated with a high dose of IL-2 alone exhibited potent cytotoxic activity. These results indicated that IL-7 was involved in the generation of immunocompetent T cells in the thymus in concert with IL-2.
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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, CD8,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Differentiation...,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-7,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, T-Cell
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
143
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2917-22
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:2572646-Animals,
pubmed-meshheading:2572646-Antigens, CD8,
pubmed-meshheading:2572646-Antigens, Differentiation, T-Lymphocyte,
pubmed-meshheading:2572646-CD4-Positive T-Lymphocytes,
pubmed-meshheading:2572646-Cells, Cultured,
pubmed-meshheading:2572646-Cytotoxicity, Immunologic,
pubmed-meshheading:2572646-Drug Synergism,
pubmed-meshheading:2572646-Flow Cytometry,
pubmed-meshheading:2572646-Interleukin-2,
pubmed-meshheading:2572646-Interleukin-7,
pubmed-meshheading:2572646-Lymphocyte Activation,
pubmed-meshheading:2572646-Mice,
pubmed-meshheading:2572646-Mice, Inbred Strains,
pubmed-meshheading:2572646-Receptors, Antigen, T-Cell,
pubmed-meshheading:2572646-Thymus Gland
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pubmed:year |
1989
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pubmed:articleTitle |
IL-7 promotes thymocyte proliferation and maintains immunocompetent thymocytes bearing alpha beta or gamma delta T-cell receptors in vitro: synergism with IL-2.
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pubmed:affiliation |
Department of Medicine, Jichi Medical School, Tochigi, Japan.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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