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肿瘤坏死因子诱导培养的人气道上皮细胞中白细胞介素-8的表达。

Tumor necrosis factor-induced interleukin-8 expression in cultured human airway epithelial cells.

作者信息

Kwon O J, Au B T, Collins P D, Adcock I M, Mak J C, Robbins R R, Chung K F, Barnes P J

机构信息

Department of Thoracic Medicine, National Heart and Lung Institute, London, United Kingdom.

出版信息

Am J Physiol. 1994 Oct;267(4 Pt 1):L398-405. doi: 10.1152/ajplung.1994.267.4.L398.

DOI:10.1152/ajplung.1994.267.4.L398
PMID:7943343
Abstract

The effects of tumor necrosis factor-alpha (TNF-alpha) on interleukin-8 (IL-8) expression and generation were examined in primary cultured human airway epithelial cells (HAEC) and a human lung epithelial cell line (A549). TNF-alpha increased IL-8 mRNA and protein expression in HAEC in a concentration- and time-dependent manner and these effects were inhibited by dexamethasone (1 microM). There was no change in the stability of IL-8 mRNA, and a nuclear run-on assay confirmed that TNF-alpha increased IL-8 gene transcription. TNF-alpha-induced IL-8 mRNA expression showed a biphasic response in HAEC, with an early increase at 2 h followed by a sustained increase from 8 h, which was abolished by the addition of cycloheximide, suggesting that the synthesis of another protein was involved. A549 cells also increased IL-8 secretion and mRNA after incubation of TNF-alpha, with inhibition by dexamethasone. However, A549 cells showed only an early single peak. A549 cells showed a 250-fold increase in the generation of IL-8 immunoreactivity, whereas primary cultured HAEC showed only a threefold increase, suggesting that HAEC and A549 cells may respond to TNF-alpha in different ways. The sustained increase in IL-8 secretion due to an increase in gene transcription in response to TNF-alpha may be an important amplification step in inflammatory diseases of the airways.

摘要

在原代培养的人气道上皮细胞(HAEC)和人肺上皮细胞系(A549)中检测了肿瘤坏死因子-α(TNF-α)对白细胞介素-8(IL-8)表达和生成的影响。TNF-α以浓度和时间依赖性方式增加HAEC中IL-8 mRNA和蛋白的表达,且这些作用被地塞米松(1μM)抑制。IL-8 mRNA的稳定性没有变化,核转录分析证实TNF-α增加了IL-8基因转录。TNF-α诱导的IL-8 mRNA表达在HAEC中呈现双相反应,2小时时有早期增加,随后从8小时起持续增加,加入环己酰亚胺后这种增加被消除,提示涉及另一种蛋白质的合成。TNF-α孵育后,A549细胞也增加了IL-8分泌和mRNA,且被地塞米松抑制。然而,A549细胞仅呈现早期单峰。A549细胞中IL-8免疫反应性的生成增加了250倍,而原代培养的HAEC仅增加了3倍,提示HAEC和A549细胞可能以不同方式对TNF-α作出反应。TNF-α导致的基因转录增加引起的IL-8分泌持续增加可能是气道炎性疾病中的一个重要放大步骤。

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