rdf:type |
|
lifeskim:mentions |
umls-concept:C0025914,
umls-concept:C0026809,
umls-concept:C0035820,
umls-concept:C0039194,
umls-concept:C0085358,
umls-concept:C0123759,
umls-concept:C0205263,
umls-concept:C1332700,
umls-concept:C1332714,
umls-concept:C1332717,
umls-concept:C1413244,
umls-concept:C1511545,
umls-concept:C1706438,
umls-concept:C2698600
|
pubmed:issue |
8
|
pubmed:dateCreated |
2001-8-13
|
pubmed:abstractText |
Despite increasing evidence for the role of the chemokine system in leukocyte trafficking, the mechanism underlying the induction of chemokine receptors is poorly understood. Here, we investigated how CCR5, a chemokine receptor implicated in T cell migration to inflammatory sites, is induced in the T cell. CCR5 mRNA was hardly detected in resting T cells and marginally induced following T cell receptor (TCR) stimulation. However, TCR-triggered T cells expressed IL-12 receptor, and stimulation with recombinant IL-12 resulted in high levels of CCR5 expression on both CD4(+) and CD8(+) T cells. In contrast, IL-2 failed to up-regulate CCR5 expression. The effect of IL-12 was selective to CCR5 because IL-12 did not up-regulate CXCR3 expression. Surface expression of CCR5 was shown by staining with anti-CCR5 monoclonal antibody. Stimulation of these CCR5-positive T cells with the relevant chemokine MIP-1 alpha elicited Ca(2+) influx, showing that IL-12-induced CCR5 is functional. These results indicate a critical role for IL-12 in the induction of CCR5 on TCR-triggered T cells.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CCL4,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-12,
http://linkedlifedata.com/resource/pubmed/chemical/Macrophage Inflammatory Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, T-Cell,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, CCR5
|
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0014-2980
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
31
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
2411-20
|
pubmed:dateRevised |
2008-11-21
|
pubmed:meshHeading |
pubmed-meshheading:11500825-Animals,
pubmed-meshheading:11500825-CD4-Positive T-Lymphocytes,
pubmed-meshheading:11500825-CD8-Positive T-Lymphocytes,
pubmed-meshheading:11500825-Calcium,
pubmed-meshheading:11500825-Calcium Signaling,
pubmed-meshheading:11500825-Cells, Cultured,
pubmed-meshheading:11500825-Chemokine CCL4,
pubmed-meshheading:11500825-Fluorescent Antibody Technique,
pubmed-meshheading:11500825-Interferon-gamma,
pubmed-meshheading:11500825-Interleukin-12,
pubmed-meshheading:11500825-Macrophage Inflammatory Proteins,
pubmed-meshheading:11500825-Mice,
pubmed-meshheading:11500825-Mice, Inbred BALB C,
pubmed-meshheading:11500825-RNA, Messenger,
pubmed-meshheading:11500825-Receptors, Antigen, T-Cell,
pubmed-meshheading:11500825-Receptors, CCR5,
pubmed-meshheading:11500825-Up-Regulation
|
pubmed:year |
2001
|
pubmed:articleTitle |
A critical role for IL-12 in CCR5 induction on T cell receptor-triggered mouse CD4(+) and CD8(+) T cells.
|
pubmed:affiliation |
Department of Oncology, Biomedical Research Center, Osaka University Graduate School of Medicine, Osaka, Japan.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|