Modulatory Roles of Interferon-γ through Indoleamine 2, 3-dioxygenase Induction in Innate Immune Response of Dental Pulp Cells

被引:15
|
作者
Takegawa, Daisuke [1 ]
Nakanishi, Tadashi [1 ]
Hirao, Kouji [1 ]
Yumoto, Hiromichi [1 ]
Takahashi, Kanako [1 ]
Matsuo, Takashi [1 ]
机构
[1] Univ Tokushima, Grad Sch, Dept Conservat Dent, Inst Hlth Biosci, Tokushima 7708504, Japan
关键词
CXCL10; indoleamine; 2; 3-dioxygenase; interleukin6; nucleotide-binding oligomerization domain; pattern recognition receptors; pulpitis; Toll-like receptors; 2,3-DIOXYGENASE EXPRESSION; TRYPTOPHAN DEGRADATION; FIBROBLASTS; TOLERANCE; MICE; PEPTIDOGLYCAN; CATABOLISM; CHEMOKINES; BACTERIA; ALPHA;
D O I
10.1016/j.joen.2014.03.018
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Introduction: Marked infiltration of inflammatory cells such as activated T cells producing interferon-gamma (IFN-gamma) is observed in severe pulpitis. However, the roles of IFN-gamma, in the innate immune response of dental pulp have not been reported. Indoleamine 2, 3-dioxygenase (IDO) is a regulator of immune responses, and the IDO expression is induced by IFN-gamma in many cells whose expression in dental pulp is unknown. The purpose of this study was to determine the role of IFN-gamma in the immune response through microbial pattern recognition receptors (PRRs) such as Toll-like receptors or nucleotide-binding oligomerization domain like receptors on the production of proinflammatory cytokines such as CXCL10 and interleukin (IL)-6 and the expression of IDO in cultured human dental pulp cells (HDPCs). Methods: HDPCs were established from explant cultures of healthy pulp tissues. CXCL10 and IL-6 production was determined using enzyme-linked immunosorbent assay. Confirmation of IDO localization in dental pulp tissues was examined using immunohistochemistry. IDO expression in HDPCs was analyzed by immunoblot. Results: IFN-gamma significantly up-regulated CXCL10 and IL-6 production in the HDPCs stimulated with ligands for PRRs in a concentration-dependent manner. The expression of IDO was detected in inflamed pulp tissue. In addition, IFN-gamma in combination with the PRR ligands enhanced 100 expression in HDPCs compared with IFN-gamma alone. Moreover, CXCL10 production in IFN-gamma stimulated HDPCs was inhibited by an IDO inhibitor. Conclusions: This study showed the synergistic effects by IFN-gamma on cytokine production and 100 expression in HDPCs, suggesting that IFN-gamma may modulate the innate immune response of dental pulp.
引用
收藏
页码:1382 / 1387
页数:6
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