| Literature DB >> 24029595 |
Won-Sik Lee1, Soung-Min Lee, Mi-Kyoung Kim, Sae-Gwang Park, Ii-Whan Choi, Inhak Choi, Young-Don Joo, Sung-Jae Park, Sun-Woo Kang, Su-Kil Seo.
Abstract
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.Entities:
Keywords: 3-Hydroxyanthranilic acid; Dendritic cells; Indoleamine 2,3-dioxygenase
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Year: 2013 PMID: 24029595 DOI: 10.1016/j.intimp.2013.08.018
Source DB: PubMed Journal: Int Immunopharmacol ISSN: 1567-5769 Impact factor: 4.932