The activity of NF-κB in Swiss 3T3 cells exposed to aqueous extracts of cigarette smoke is dependent on thioredoxin

被引:35
作者
Gebel, S [1 ]
Müller, T [1 ]
机构
[1] INBIFO, Inst Biol Forschung, D-51149 Cologne, Germany
关键词
cigarette smoke; NF-kappa B; thioredoxin; thiol oxidation; glutathione;
D O I
10.1093/toxsci/59.1.75
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Multiple studies in vitro have demonstrated that aqueous extracts of mainstream cigarette smoke (CS) [smoke-bubbled phosphate-buffered saline (PBS)] induce a distinct pattern of stress response in cultured cells, which may be related to the reported pro-inflammatory activities of CS in vitro and in vivo. Nuclear factor kappaB (NF-kappaB) is a transcription factor involved in both inflammatory and stress-dependent cell-signaling processes. Here we report on the activity of NF-kappaB in cells exposed to subcytotoxic concentrations of smoke-bubbled PBS. Using electrophoretic mobility shift assay (EMSA) techniques, we observed a decreased DNA binding of NF-kappaB during the first 2 h of exposure, which was followed by a more than 2-fold increase over controls after 4 to 6 h of exposure, This type of kinetics is not regulated by I kappaB-alpha, as evidenced by the lack of phosphorylation and degradation of I kappaB-alpha in CS-treated cells, However, as demonstrated in immunocoprecipitation experiments, the kinetics of NF-kappaB DNA binding is strictly paralleled by decreased and increased complex formation between NF-kappaB and thioredoxin (Trx), the reducing catalyst of Cys-62 of NF-kappaB subunit p50, the reduced thiol function of which is essential for efficient NF-kappaB DNA binding. Monitoring the expression of the gene encoding thioredoxin reductase (TrxR), which is required to keep Trx in a functional reduced state, we observed a significant increase in TrxR mRNA after 2 to 6 h of exposure. Based on the correspondence between the kinetics of NF-kappaB DNA binding, NF-kappaB/Trx complex formation, and TrxR expression, along with a lack of I kappaB-alpha phosphorylation and degradation, these results suggest that the activity of NF-kappaB in CS-treated cells is subject mainly to a redox-controlled mechanism dependent on the availability of reduced Trx rather than being controlled by its normal regulator, I kappaB-alpha.
引用
收藏
页码:75 / 81
页数:7
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