Lüling Robin, John Harald, Gudermann Thomas, Thiermann Horst, Mückter Harald, Popp Tanja, Steinritz Dirk
Bundeswehr Institute of Pharmacology and Toxicology, Ludwig-Maximilians-Universität Munich, 80937 Munich, Germany.
Walther-Straub-Institute of Pharmacology and Toxicology, Ludwig-Maximilians-Universität Munich, 80336 Munich, Germany.
Cells. 2018 Aug 31;7(9):126. doi: 10.3390/cells7090126.
The chemosensory transient receptor potential ankyrin 1 (TRPA1) ion channel perceives different sensory stimuli. It also interacts with reactive exogenous compounds including the chemical warfare agent sulfur mustard (SM). Activation of TRPA1 by SM results in elevation of intracellular calcium levels but the cellular consequences are not understood so far. In the present study we analyzed SM-induced and TRPA1-mediated effects in human TRPA1-overexpressing HEK cells (HEKA1) and human lung epithelial cells (A549) that endogenously exhibit TRPA1. The specific TRPA1 inhibitor AP18 was used to distinguish between SM-induced and TRPA1-mediated or TRPA1-independent effects. Cells were exposed to 600 µM SM and proteome changes were investigated 24 h afterwards by 2D gel electrophoresis. Protein spots with differential staining levels were analyzed by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry and nano liquid chromatography electrospray ionization tandem mass spectrometry. Results were verified by RT-qPCR experiments in both HEKA1 or A549 cells. Heat shock 70 kDa protein 6 () was identified as an SM-induced and TRPA1-mediated protein. AP18 pre-treatment diminished the up-regulation. RT-qPCR measurements verified these results and further revealed a time-dependent regulation. Our results demonstrate that SM-mediated activation of TRPA1 influences the protein expression and confirm the important role of TRPA1 ion channels in the molecular toxicology of SM.
化学感觉瞬时受体电位锚蛋白1(TRPA1)离子通道能感知不同的感觉刺激。它还与包括化学战剂硫芥(SM)在内的反应性外源性化合物相互作用。SM激活TRPA1会导致细胞内钙水平升高,但目前尚不清楚其细胞后果。在本研究中,我们分析了SM诱导的以及TRPA1介导的对过表达人TRPA1的HEK细胞(HEKA1)和内源性表达TRPA1的人肺上皮细胞(A549)的影响。使用特异性TRPA1抑制剂AP18来区分SM诱导的、TRPA1介导的或TRPA1非依赖性的效应。将细胞暴露于600μM SM中,24小时后通过二维凝胶电泳研究蛋白质组变化。通过基质辅助激光解吸/电离飞行时间质谱和纳升液相色谱电喷雾电离串联质谱分析染色水平有差异的蛋白质斑点。在HEKA1或A549细胞中通过RT-qPCR实验验证结果。热休克70 kDa蛋白6()被鉴定为一种SM诱导的且由TRPA1介导的蛋白。AP18预处理减弱了上调。RT-qPCR测量验证了这些结果,并进一步揭示了时间依赖性调节。我们的结果表明,SM介导的TRPA1激活影响蛋白质表达,并证实了TRPA1离子通道在SM分子毒理学中的重要作用。