Price Katherine A, Filiz Gulay, Caragounis Aphrodite, Du Tai, Laughton Katrina M, Masters Colin L, Sharples Robyn A, Hill Andrew F, Li Qiao-Xin, Donnelly Paul S, Barnham Kevin J, Crouch Peter J, White Anthony R
Department of Pathology, The University of Melbourne, Victoria 3010, Australia.
Int J Biochem Cell Biol. 2008;40(9):1901-17. doi: 10.1016/j.biocel.2008.01.033. Epub 2008 Feb 12.
The epidermal growth factor receptor is a receptor tyrosine kinase expressed in a range of tissues and cell-types. Activation of the epidermal growth factor receptor by a number of ligands induces downstream signalling that modulates critical cell functions including growth, survival and differentiation. Abnormal epidermal growth factor receptor expression and activation is also involved in a number of cancers. In addition to its cognate ligands, the epidermal growth factor receptor can be activated by metals such as zinc (Zn) and copper (Cu). Due to the important role of these metals in a number of diseases including neurodegenerative disorders, therapeutic approaches are being developed based on the use of lipid permeable metal-complexing molecules. While these agents are showing promising results in animal models and clinical trials, little is known about the effects of metal-ligand complexes on cell signalling pathways. In this study, we investigated the effects of clioquinol (CQ)-metal complexes on activation of epidermal growth factor receptor. We show here that CQ-Cu complexes induced potent epidermal growth factor receptor phosphorylation resulting in downstream activation of extracellular signal-regulated kinase. Similar levels of epidermal growth factor receptor activation were observed with alternative lipid permeable metal-ligands including neocuproine and pyrrolidine dithiocarbamate. We found that CQ-Cu complexes induced a significant reduction in the level of extracellular Abeta1-40 in cell culture. Inhibition of epidermal growth factor receptor activation by PD153035 blocked extracellular signal-regulated kinase phosphorylation and restored Abeta1-40 levels. Activation of the epidermal growth factor receptor by CQ-Cu was mediated through up-regulation of src kinase activity by a cognate ligand-independent process involving membrane integrins. These findings provide the first evidence that metal-ligand complexes can activate the epidermal growth factor receptor with potentially neuroprotective effects.
表皮生长因子受体是一种受体酪氨酸激酶,在多种组织和细胞类型中表达。多种配体激活表皮生长因子受体可诱导下游信号传导,从而调节包括生长、存活和分化在内的关键细胞功能。表皮生长因子受体的异常表达和激活也与多种癌症有关。除了其同源配体,表皮生长因子受体还可被锌(Zn)和铜(Cu)等金属激活。由于这些金属在包括神经退行性疾病在内的多种疾病中具有重要作用,基于使用脂质可渗透金属络合分子的治疗方法正在被开发。虽然这些药物在动物模型和临床试验中显示出有前景的结果,但对于金属 - 配体复合物对细胞信号通路的影响知之甚少。在本研究中,我们研究了氯碘羟喹(CQ) - 金属络合物对表皮生长因子受体激活的影响。我们在此表明,CQ - Cu络合物诱导表皮生长因子受体有效磷酸化,导致细胞外信号调节激酶的下游激活。使用包括新亚铜试剂和吡咯烷二硫代氨基甲酸盐在内的替代脂质可渗透金属配体也观察到了类似水平的表皮生长因子受体激活。我们发现CQ - Cu络合物在细胞培养中诱导细胞外β淀粉样蛋白1 - 40水平显著降低。用PD153035抑制表皮生长因子受体激活可阻断细胞外信号调节激酶磷酸化并恢复β淀粉样蛋白1 - 40水平。CQ - Cu对表皮生长因子受体的激活是通过一种涉及膜整合素的同源配体非依赖性过程上调src激酶活性介导的。这些发现提供了首个证据,表明金属 - 配体复合物可激活表皮生长因子受体并具有潜在的神经保护作用。