The involvement of the Toll-like receptor signaling and Nrf2-Keap1 pathways in the in vitro regulation of IL-8 and HMOX1 for skin sensitization

被引:7
作者
van der Veen, Jochem W. [1 ,2 ]
Paskel, Ruthmila F. [1 ]
Smits, Noortje A. M. [1 ]
Hodemaekers, Henny [1 ]
van Loveren, Henk [1 ,2 ]
Ezendam, Janine [1 ]
机构
[1] Natl Inst Publ Hlth & Environm RIVM, POB 1, NL-3720 BA Bilthoven, Netherlands
[2] Maastricht Univ, Dept Toxicogenom, NL-6200 MD Maastricht, Netherlands
关键词
Heme oxygenase 1; IL-8; immunotoxicology; Nrf2-Keap1; pathway; siRNA; skin sensitization; toll-like receptor signaling; GENE-EXPRESSION; THP-1; CELLS; ACTIVATION; SIGNATURE; RELEASE; NRF2;
D O I
10.3109/1547691X.2014.975897
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
In vitro gene profiling studies have associated the molecular pathways of Nrf2-Keap1 and Toll-like receptor (TLR) signaling with skin sensitization. In this study, the role of these pathways in the regulation of protein biomarkers for skin sensitization was further elucidated using transient gene knock-down of key components of the signaling cascades in HaCaT cells after exposure to dinitrochlorobenzene (DNCB). The effect of targeting these pathways was established through evaluation of heme oxygenase1 (HMOX1) and interleukin (IL)-8 production. These experiments showed that Nrf2 is not involved in regulating HMOX1 after exposure to DNCB, but that activation of TLR signaling moderates the expression of HMOX1. The regulation of IL-8 depended on Nrf2, but also on the Toll/interleukin-1 receptor (TIR)-domain-containing adapter-inducing interferon-beta (TRIF) adaptor protein in TLR signaling. This study provides new insights into the regulation of HMOX1 and IL-8, but the exact regulating mechanisms remain to be further elucidated.
引用
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页码:1 / 6
页数:6
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