Driscoll K E, Carter J M, Howard B W, Hassenbein D, Janssen Y M, Mossman B T
Procter & Gamble Pharmaceuticals, Health Care Research Center, Cincinnati, OH 45040-8006, USA.
Environ Health Perspect. 1998 Oct;106 Suppl 5(Suppl 5):1171-4. doi: 10.1289/ehp.98106s51171.
Nuclear factor kappa B (NF-kappa B) is a transcription factor that regulates expression of several genes coding for inflammatory and immunoregulatory proteins including the neutrophil chemotactic cytokine MIP-2. In previous studies we found that crocidolite asbestos activates the nuclear translocation of NF-kappa B as well as MIP-2 gene expression in rat alveolar type II cells. Here we report that both crocidolite-induced NF-kappa B activation of MIP-2 gene expression can be attenuated by the antioxidant tetramethylthiourea, suggesting the dependence of these responses on oxidative stress. Crocidolite exposure of RLE-TN cells also increased production of H2O2, a response that was inhibited by the mitochondrial respiratory chain inhibitor thenoyltrifluoroacetone (TTFA). TTFA treatment of RLE-6TN cells also inhibited crocidolite-induced nuclear translocation of NF-kappa B and MIP-2 gene expression. These results indicate crocidolite exposure of rat alveolar type II cells results in increased production of mitochondrial-derived hydrogen peroxide and that mitochondrial-derived oxidants contribute to crocidolite activation of NF-kappa B and increases in MIP-2 gene expression.
核因子κB(NF-κB)是一种转录因子,可调节多种编码炎症和免疫调节蛋白的基因的表达,包括中性粒细胞趋化细胞因子MIP-2。在先前的研究中,我们发现青石棉可激活大鼠肺泡II型细胞中NF-κB的核转位以及MIP-2基因的表达。在此我们报告,抗氧化剂四甲基硫脲可减弱青石棉诱导的NF-κB激活和MIP-2基因表达,这表明这些反应依赖于氧化应激。RLE-TN细胞暴露于青石棉也会增加过氧化氢的产生,线粒体呼吸链抑制剂噻吩甲酰三氟丙酮(TTFA)可抑制这一反应。用TTFA处理RLE-6TN细胞也可抑制青石棉诱导的NF-κB核转位和MIP-2基因表达。这些结果表明,大鼠肺泡II型细胞暴露于青石棉会导致线粒体衍生的过氧化氢产生增加,并且线粒体衍生的氧化剂有助于青石棉激活NF-κB并增加MIP-2基因表达。