Knickelbein Jared E, de Souza Anjali J, Tosti Richard, Narayan Preeti, Kane Lawrence P
Department of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.
J Immunol. 2006 Oct 15;177(8):4966-70. doi: 10.4049/jimmunol.177.8.4966.
T cell Ig and mucin domain protein 2 (TIM-2) has been shown to regulate T cell activation in vitro and T cell-mediated disease in vivo. However, it is still not clear whether TIM-2 acts mainly to augment T cell function or to inhibit it. We have directly examined the function of TIM-2 in murine and human T cell lines. Our results indicate that expression of TIM-2 significantly impairs the induction of NFAT and AP-1 transcriptional reporters by not only TCR ligation but also by the pharmacological stimuli PMA and ionomycin. This does not appear to be due to a general effect on cell viability, and the block in NFAT activation can be bypassed by expression of activated alleles of Ras or calcineurin, or MEK kinase, in the case of AP-1. Thus, our data are consistent with a model whereby TIM-2 inhibits T cell activation.
T细胞免疫球蛋白和粘蛋白结构域蛋白2(TIM-2)已被证明在体外可调节T细胞活化,在体内可调节T细胞介导的疾病。然而,TIM-2主要是增强还是抑制T细胞功能仍不清楚。我们直接检测了TIM-2在小鼠和人类T细胞系中的功能。我们的结果表明,TIM-2的表达不仅通过TCR连接,而且通过药理刺激佛波酯(PMA)和离子霉素,显著损害NFAT和AP-1转录报告基因的诱导。这似乎不是对细胞活力的普遍影响,并且在AP-1的情况下,Ras、钙调神经磷酸酶或MEK激酶的活化等位基因的表达可以绕过NFAT激活的阻滞。因此,我们的数据与TIM-2抑制T细胞活化的模型一致。