NFAT1 and NFAT2 Differentially Regulate IL-17A Expression in Human T Cells

被引:5
作者
Kaminuma, Osamu [1 ]
Kitamura, Noriko [2 ]
Mori, Akio [2 ]
Tatsumi, Hideki [3 ]
Nemoto, Soichi [3 ]
Hiroi, Takachika
机构
[1] Tokyo Metropolitan Inst Med Sci, Dept Allergy & Immunol, Setagaya Ku, Tokyo 1568506, Japan
[2] Sagamihara Natl Hosp, Clin Res Ctr Allergy & Rheumatol, Sagamihara, Kanagawa, Japan
[3] Sagamihara Natl Hosp, Dept Obstet & Gynecol, Natl Hosp Org, Sagamihara, Kanagawa, Japan
基金
日本学术振兴会;
关键词
Human T cell; Immunosuppressant; NFAT; Th17; NUCLEAR FACTOR; TRANSCRIPTIONAL REGULATION; CALCINEURIN; ACTIVATION; INTERLEUKIN-17; TARGET; GENES;
D O I
10.1159/000337757
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: The NFAT family transcription factors play crucial roles in T cell functions. Recently, NFAT has been implicated in the production of an inflammatory cytokine, IL-17A; however, functional differences among NFAT members in IL-17A synthesis have not been elucidated. In this study, the relative contribution of NFAT1 and NFAT2 to IL-17A expression in human T cells was investigated. Methods: NFAT1 and NFAT2 were introduced in human cord blood CD4+ T cells by a lentiviral transduction system. Then, the expression of IL-17A mRNA was determined by quantitative real-time RT-PCR. The transient effects of NFAT1 and NFAT2 on IL-17A expression in Jurkat-Tag cells were also investigated. Results: Stimulation-induced expression of IL-17A in human CD4+ T cells was augmented by the introduction of NFAT1 and more vigorously, NFAT2. IL-17A expression in Jurkat-Tag cells was also enhanced by NFAT1, whereas it was not affected by NFAT2. Conclusion: NFAT1 and NFAT2 facilitated IL-17A expression in human T cells, though distinct mechanisms might be involved in these effects. Copyright (C) 2012 S. Karger AG, Basel
引用
收藏
页码:30 / 34
页数:5
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