Bland Christin, Rand Matthew D
Department of Anatomy and Neurobiology, College of Medicine, University of Vermont, 426C HSRF, 149 Beaumont Avenue, Burlington, VT 05405, USA.
Neurotoxicology. 2006 Dec;27(6):982-91. doi: 10.1016/j.neuro.2006.04.005. Epub 2006 Apr 28.
Methylmercury (MeHg) toxicity in humans manifests deficits in neurological function. Cases of prenatal exposure to mercury have established that the developing nervous system is most highly susceptible to perturbation by MeHg. At a cellular level, MeHg-induced defects result from altered neuronal proliferation, migration and pathfinding. However, the molecular targets of MeHg that give rise to these outcomes are not fully understood. In an overall effort to identify the fundamental molecular targets of MeHg in neural development, we have explored the effects of MeHg on cell surface receptor function using the simplified Drosophila model. In this study, we investigated the potential role of MeHg to alter activity of the Notch receptor pathway, a highly conserved cell-cell signaling mechanism that controls cell fate decisions, proliferation, migration and neurite outgrowth in neural development. Notch receptor activation requires proteolysis by a cell surface ADAM metalloprotease. ADAM proteases are required for normal neural development and are activated by organomercurials, thus presenting a possible mechanism for MeHg neurotoxicity. Here, we demonstrate a concentration- and time-dependent increase in Notch receptor activity with MeHg exposure in three distinct Drosophila cell lines. Ten micromolar MeHg results in a 4-5.5-fold increase in Notch signaling as measured by the upregulation of two enhancer of split (E(spl)) target genes. MeHg-induced Notch activity also correlates with receptor proteolysis. Targeted knockdown of Notch protein expression demonstrates that MeHg induced E(spl) activation specifically requires the Notch receptor. Furthermore, MeHg-induced Notch activity is partially attenuated by the metalloprotease inhibitor, GM6001, consistent with a model in which MeHg promotes activation of ADAM metalloproteases. Finally, we demonstrate that inorganic HgCl(2) is significantly less active in inducing Notch activity, suggesting a mechanism specific to organic species of mercury. Overall, these data identify Notch as a potential target for MeHg toxicity in the developing nervous system.
甲基汞(MeHg)对人类的毒性表现为神经功能缺陷。产前接触汞的案例已证实,发育中的神经系统对MeHg的干扰最为敏感。在细胞水平上,MeHg诱导的缺陷源于神经元增殖、迁移和路径寻找的改变。然而,导致这些结果的MeHg分子靶点尚未完全明确。为了全面确定MeHg在神经发育中的基本分子靶点,我们利用简化的果蝇模型探索了MeHg对细胞表面受体功能的影响。在本研究中,我们调查了MeHg改变Notch受体途径活性的潜在作用,Notch受体途径是一种高度保守的细胞间信号传导机制,在神经发育中控制细胞命运决定、增殖、迁移和神经突生长。Notch受体激活需要细胞表面ADAM金属蛋白酶进行蛋白水解。ADAM蛋白酶是正常神经发育所必需的,并且可被有机汞激活,因此这可能是MeHg神经毒性的一种机制。在此,我们证明在三种不同的果蝇细胞系中,随着MeHg暴露,Notch受体活性呈现浓度和时间依赖性增加。通过两个分裂增强子(E(spl))靶基因的上调来衡量,10微摩尔的MeHg会导致Notch信号增加4至5.5倍。MeHg诱导的Notch活性也与受体蛋白水解相关。靶向敲低Notch蛋白表达表明,MeHg诱导的E(spl)激活特别需要Notch受体。此外,金属蛋白酶抑制剂GM60降低了MeHg诱导的Notch活性,这与MeHg促进ADAM金属蛋白酶激活的模型一致。最后,我们证明无机HgCl₂在诱导Notch活性方面的活性明显较低,这表明汞的有机物种具有特定的机制。总体而言,这些数据表明Notch是发育中神经系统中MeHg毒性的潜在靶点。