Department of Hemato/Oncology, Busan Paik Hospital, College of Medicine, Inje University, Busan 614-735, South Korea.
Int Immunopharmacol. 2013 Nov;17(3):721-6. doi: 10.1016/j.intimp.2013.08.018. Epub 2013 Sep 9.
The generation of tryptophan (Trp) metabolites by indoleamine 2,3-dioxygenase (IDO) is an effective mechanism for T cell suppression. However, the effect of Trp metabolites on dendritic cells (DCs) remains unclear. Here, we investigated whether the tryptophan metabolite 3-hydroxyanthranilic acid (3-HAA) directly inhibits DC activation and is responsible for T cell suppression. We found that 3-HAA treatment significantly reduced IL-12, IL-6, and TNF-α production in bone marrow-derived DCs (BMDCs) stimulated with LPS. Maturation markers CD40, CD80, CD86, and I-A were also significantly reduced. Moreover, treatment with 3-HAA decreased the ability of DCs to stimulate T cell activation and differentiation in vitro and in vivo. Finally, we observed that phospho-JNK and phospho-38 levels were reduced in 3-HAA-treated DC2.4 cells and BMDCs. These results suggest that the tryptophan metabolite 3-HAA suppresses T cell responses by inhibiting DC activation.
色氨酸(Trp)代谢物的生成吲哚胺 2,3-双加氧酶(IDO)是 T 细胞抑制的有效机制。然而,色氨酸代谢物对树突状细胞(DC)的影响尚不清楚。在这里,我们研究了色氨酸代谢物 3-羟基邻氨基苯甲酸(3-HAA)是否直接抑制 DC 的激活并导致 T 细胞抑制。我们发现,3-HAA 处理可显著降低 LPS 刺激的骨髓来源的树突状细胞(BMDC)中 IL-12、IL-6 和 TNF-α的产生。成熟标志物 CD40、CD80、CD86 和 I-A 也显著降低。此外,3-HAA 处理降低了 DC 在体外和体内刺激 T 细胞活化和分化的能力。最后,我们观察到 3-HAA 处理的 DC2.4 细胞和 BMDC 中的磷酸化-JNK 和磷酸化-38 水平降低。这些结果表明,色氨酸代谢物 3-HAA 通过抑制 DC 的激活来抑制 T 细胞反应。