IWASAKI Masayuki
Department Research Institutes and Facilities, Research Institutes and Facilities Position Assistant Professor |
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Article types | Original article |
Language | English |
Peer review | Peer reviewed |
Title | A critical role for IL-12 in CCR5 induction on T cell receptor-triggered mouse CD4(+) and CD8(+) T cells. |
Journal | Formal name:European journal of immunology Abbreviation:Eur J Immunol ISSN code:00142980/00142980 |
Domestic / Foregin | Foregin |
Volume, Issue, Page | 31(8),pp.2411-20 |
Author and coauthor | Iwasaki M, Mukai T, Gao P, Park W R, Nakajima C, Tomura M, Fujiwara H, Hamaoka T |
Authorship | Lead author |
Publication date | 2001/08 |
Summary | 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. |
DOI | 10.1002/1521-4141(200108)31:8<2411::aid-immu2411>3.0.co;2-y |
PMID | 11500825 |