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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1997-7-22
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pubmed:abstractText |
The C-C chemokine RANTES, a T lymphocyte chemoattractant, is considered an important mediator of inflammation, allergy, and host defense against HIV-1 infection. In this study, we investigated the modulation of binding of RANTES to T lymphocytes. Human peripheral blood CD3+ T cells, when freshly isolated from buffy-coat blood, expressed a considerable number of high-affinity binding sites for RANTES. These cells also showed significant chemotactic migration in response to RANTES in vitro. After 6-15 h incubation at 37 degrees C, the binding of RANTES, but not of macrophage inflammatory protein-1 alpha (MIP-1 alpha) or of monocyte chemotactic protein-3 (MCP-3), consistently increased. Scatchard analyses indicated that the number of binding sites for RANTES increased about threefold by 15 h without any change in the affinity. The increase in RANTES binding was no longer detected by 24 h. This increase in the specific binding was mainly attributable to CD4+ T cells and was not associated with increased chemotactic activity of these cells in response to RANTES. Incubation with anti-CD3 antibody for 15 h markedly reduced the binding capability of T cells for RANTES and was associated with decreased chemotactic activity. On the other hand, when T cells were incubated with interleukin-2 (IL-2) for 1 week, the specific binding for all three C-C chemokines, RANTES, MIP-1 alpha, and MCP-3 was markedly increased in comparison to cells cultured in the absence of IL-2. These results suggest that the expression of binding sites on T cells for RANTES is differentially modulated, indicating the existence of novel receptors for RANTES that do not bind MIP-1 alpha.
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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/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD3,
http://linkedlifedata.com/resource/pubmed/chemical/CCL7 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CCL4,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CCL5,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CCL7,
http://linkedlifedata.com/resource/pubmed/chemical/Cytokines,
http://linkedlifedata.com/resource/pubmed/chemical/Iodine Radioisotopes,
http://linkedlifedata.com/resource/pubmed/chemical/Macrophage Inflammatory Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Monocyte Chemoattractant Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0014-2980
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
27
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1406-12
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:9209492-Antibodies, Monoclonal,
pubmed-meshheading:9209492-Antigens, CD3,
pubmed-meshheading:9209492-Binding Sites,
pubmed-meshheading:9209492-CD4-Positive T-Lymphocytes,
pubmed-meshheading:9209492-CD8-Positive T-Lymphocytes,
pubmed-meshheading:9209492-Chemokine CCL4,
pubmed-meshheading:9209492-Chemokine CCL5,
pubmed-meshheading:9209492-Chemokine CCL7,
pubmed-meshheading:9209492-Cytokines,
pubmed-meshheading:9209492-Down-Regulation,
pubmed-meshheading:9209492-Humans,
pubmed-meshheading:9209492-Iodine Radioisotopes,
pubmed-meshheading:9209492-Kinetics,
pubmed-meshheading:9209492-Macrophage Inflammatory Proteins,
pubmed-meshheading:9209492-Monocyte Chemoattractant Proteins,
pubmed-meshheading:9209492-Protein Binding,
pubmed-meshheading:9209492-T-Lymphocyte Subsets
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pubmed:year |
1997
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pubmed:articleTitle |
Differential expression of binding sites for chemokine RANTES on human T lymphocytes.
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pubmed:affiliation |
Laboratory of Molecular Immunoregulation, National Cancer Institute-Frederick Cancer Research and Development Center, MD 21702, USA.
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pubmed:publicationType |
Journal Article,
Comparative Study
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