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首页> 外文期刊>Mediators of inflammation >Pro-inflammatory cytokines induce c-fos expression followed by IL-6 release in human airway smooth muscle cells
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Pro-inflammatory cytokines induce c-fos expression followed by IL-6 release in human airway smooth muscle cells

机译:促炎细胞因子诱导c-fos表达,然后在人气道平滑肌细胞中释放IL-6

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Background: Airway smooth muscle (ASM) is considered to be a target for mediators released during airway inflammation.Aims: To investigate the expression of c-fos, a constituent of the transcription factor activator protein-1, in human ASM cells. In addition, to measure the release of interleukin (IL)-6 into the conditioned medium of stimulated ASM cells, as well as DNA biosynthesis and changes in cell number.Methods: Serum-deprived human ASM cells in the G0/G1phase were stimulated with the pro-inflammatory cytokines; tumour necrosis factor-α, IL-1β, IL-5 and IL-6. The expression of mRNA encoding the proto-oncogene c-fos was measured by Northern blot analysis. Cell proliferation was assessed by {3H}-thymidine incorporation assays and cell counting, and IL-6 levels in cell-conditioned medium were measured by enzyme-linked immunosorbent assay.Results: All of the cytokines investigated induced a rapid (within 1h) and transient increase in the expression of mRNA encoding c-fos, followed by the expression and enhanced release of IL-6. Cell proliferation remained unchanged in cytokine-stimulated cells.Conclusions: Cytokine-induced c-fos expression in human ASM cells could be described as a marker of cell ‘activation'. The possible association of these results with airway inflammation, through secondary intracellular mechanisms such as cytokine production, is discussed.
机译:背景:气道平滑肌(ASM)被认为是气道炎症过程中释放的介质的目标。目的:研究c-fos(转录因子激活蛋白1的组成部分)在人ASM细胞中的表达。此外,测量白介素(IL)-6释放到刺激的ASM细胞的条件培养基中,以及DNA的合成和细胞数量的变化。方法:用G0 / G1期刺激血清缺乏的人ASM细胞。促炎细胞因子;肿瘤坏死因子-α,IL-1β,IL-5和IL-6。通过Northern印迹分析测量编码原癌基因c-fos的mRNA的表达。通过{3H}-胸苷掺入试验和细胞计数来评估细胞增殖,并通过酶联免疫吸附测定法测量细胞条件培养基中的IL-6水平。结果:所有研究的细胞因子均诱导了快速(1h内)和编码c-fos的mRNA表达瞬时增加,随后IL-6表达增加并释放。结论:细胞因子诱导的人ASM细胞中c-fos表达可能被描述为细胞“激活”的标志物。通过次要的细胞内机制,例如细胞因子的产生,讨论了这些结果与气道炎症的可能联系。

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