Lightfoot Adam P, Sakellariou Giorgos K, Nye Gareth A, McArdle Francis, Jackson Malcolm J, Griffiths Richard D, McArdle Anne
MRC-Arthritis UK Centre for Integrated Research into Musculoskeletal Ageing, University of Liverpool, United Kingdom.
MRC-Arthritis UK Centre for Integrated Research into Musculoskeletal Ageing, University of Liverpool, United Kingdom.
Redox Biol. 2015 Dec;6:253-259. doi: 10.1016/j.redox.2015.08.007. Epub 2015 Aug 10.
TNF-α is a key inflammatory mediator and is proposed to induce transcriptional responses via the mitochondrial generation of Reactive Oxygen Species (ROS). The aim of this study was to determine the effect of TNF-α on the production of myokines by skeletal muscle. Significant increases were seen in the release of IL-6, MCP-1/CCL2, RANTES/CCL5 and KC/CXCL1 and this release was inhibited by treatment with Brefeldin A, suggesting a golgi-mediated release of cytokines by muscle cells. An increase was also seen in superoxide in response to treatment with TNF-α, which was localised to the mitochondria and this was also associated with activation of NF-κB. The changes in superoxide, activation of NF-kB and release of myokines were attenuated following pre-treatment with SS-31 peptide indicating that the ability of TNF-α to induce myokine release may be mediated through mitochondrial superoxide, which is, at least in part, associated with activation of the redox sensitive transcription factor NF-kB.
肿瘤坏死因子-α(TNF-α)是一种关键的炎症介质,有人提出它通过线粒体产生活性氧(ROS)来诱导转录反应。本研究的目的是确定TNF-α对骨骼肌产生肌动蛋白的影响。白细胞介素-6(IL-6)、单核细胞趋化蛋白-1/CCL2、调节激活正常T细胞表达和分泌因子/CCL5以及KC/CXCL1的释放显著增加,且布雷菲德菌素A处理可抑制这种释放,这表明肌肉细胞通过高尔基体介导释放细胞因子。在用TNF-α处理后,超氧化物也有所增加,其定位于线粒体,这也与核因子-κB(NF-κB)的激活有关。用SS-31肽预处理后,超氧化物的变化、NF-κB的激活以及肌动蛋白的释放均减弱,这表明TNF-α诱导肌动蛋白释放的能力可能是通过线粒体超氧化物介导的,而线粒体超氧化物至少部分与氧化还原敏感转录因子NF-κB的激活有关。