Barth Lisa-Marie, Rink Lothar, Wessels Inga
Institute of Immunology, Medical Faculty, RWTH Aachen University, Pauwelsstraße 30, D-52074 Aachen, Germany.
Int J Mol Sci. 2020 Dec 30;22(1):326. doi: 10.3390/ijms22010326.
(1) Background: Zinc is suggested to play a major role in epidermal growth factor (EGF)-induced cell regeneration and proliferation. To deepen the knowledge on the underlying mechanisms zinc's effects on the epidermal growth factor receptor (EGFR) activation and its endocytosis was investigated in the alveolar carcinoma cell line A549. (2) Methods: An increase of intracellular zinc was generated by adding zinc extracellularly compared to the intracellular release of zinc from zinc-binding proteins by stimulation with a nitric oxide donor. Zinc-initiated EGFR phosphorylation was checked by Western blotting and receptor endocytosis assays were performed by using flow cytometry. (3) Results: Besides a dose-dependent EGFR phosphorylation, a dose- and time dependent significant receptor internalisation was initiated by both types of zinc increases. In addition, both increased intracellular zinc levels further promoted EGF-induced EGFR phosphorylation and internalisation. (4) Conclusion: This report confirms a transactivating effect of zinc on the EGFR for A549 cells and is the first describing an influence of zinc on the EGFR endocytosis. The transferability of the fine-tuning of EGFR-induced signalling by zinc needs to be verified in vivo, but the presented data underline that zinc might be helpful during treatment of disturbed regeneration and tissue repair.
(1) 背景:锌被认为在表皮生长因子(EGF)诱导的细胞再生和增殖中起主要作用。为了深入了解其潜在机制,在肺泡癌细胞系A549中研究了锌对表皮生长因子受体(EGFR)激活及其内吞作用的影响。(2) 方法:与通过一氧化氮供体刺激从锌结合蛋白释放细胞内锌相比,通过细胞外添加锌来增加细胞内锌含量。通过蛋白质免疫印迹法检测锌引发的EGFR磷酸化,并使用流式细胞术进行受体内吞作用测定。(3) 结果:除了剂量依赖性的EGFR磷酸化外,两种类型的锌增加均引发了剂量和时间依赖性的显著受体内化。此外,两种增加的细胞内锌水平进一步促进了EGF诱导的EGFR磷酸化和内化。(4) 结论:本报告证实了锌对A549细胞EGFR的反式激活作用,并且首次描述了锌对EGFR内吞作用的影响。锌对EGFR诱导信号的微调的可转移性需要在体内进行验证,但所呈现的数据强调锌在治疗再生和组织修复紊乱期间可能是有帮助的。