Cellular Mechanisms of Neuronal Metal Transport and Toxicity

描述（由申请人提供）：锌在细胞中起着重要和不同的作用，但过量的游离锌与金属细胞毒性有关。为了平衡这些相反的作用，细胞已经进化出控制细胞质金属浓度的通用机制。细胞通过将锌挤出到细胞外空间、通过胞质伴侣螯合或在细胞内隔室内隔离来实现这一目标。这最后一种机制是探讨较少的进程，它构成了我们建议的主要重点。锌在突触生理学以及急性和慢性病理条件中起着重要作用，从兴奋性毒性到神经退行性疾病特征性淀粉样蛋白聚集体的形成。尽管锌具有这些基本作用，但我们对细胞内隔室在金属螯合和体内平衡中的贡献的理解是有限的。在神经元中，细胞器锌通过突触囊泡特异性锌转运蛋白ZnT3的活性储存在突触囊泡（SV）中。我们已经分离和其特征在于蛋白质组学的ZnT3富集囊泡人口。在这些囊泡中，我们已经确定了约140个分子靶点，其中几个上调或下调囊泡内体锌储存。这些分子提供了一套独特的工具来评估细胞内细胞器，特别是内体和SV，在正常和病理性金属稳态的作用。我们的研究表明，ZnT3转运功能的调节隔室中的ZnT3转运蛋白驻留的性质。与这一概念相一致，我们已经确定了三个控制ZnT3亚细胞定位的靶向机制，这些机制具有调节ZnT3锌转运功能的潜力。在这项提案中，我们将专门探讨这些新的监管范式测试的假设，内体特异性锌转运蛋白的相互作用调节锌转运蛋白的活性和抵抗金属诱导的细胞毒性。

DESCRIPTION (provided by applicant): Zinc plays fundamental and diverse roles in cells yet excess free zinc is associated with metal cytotoxicity. To balance these opposing effects, cells have evolved universal mechanisms controlling cytoplasmic metal concentration. Cells accomplish this goal by zinc extrusion into the extracellular space, chelation by cytosolic chaperones, or sequestration within intracellular compartments. This last mechanism is the less explored process and it constitutes the main focus of our proposal. Zinc plays fundamental roles in synaptic physiology as well as in acute and chronic pathological conditions, ranging from excitotoxicity to the formation of amyloid aggregates characteristic of neurodegenerative diseases. Despite these fundamental roles of zinc, our understanding of the contribution of intracellular compartment in metal sequestration and homoeostasis is limited. In neurons, organellar zinc is stored in synaptic vesicles (SVs) by the activity of a synaptic vesicle specific zinc transporter, ZnT3. We have isolated and characterized by proteomics a ZnT3- enriched vesicle population. In these vesicles, we have identified ~ 140 molecular targets, several of which either up- or down-regulate vesicular endosomal zinc stores. These molecules provide a unique set of tools to assess the role of intracellular organelles, en particular endosomes and SV, in normal and pathological metal homeostasis. Our studies suggest that ZnT3 transport function are regulated by the nature of the compartment in which the ZnT3 transporter resides. Consistent with this notion, we have identified three targeting mechanisms that control ZnT3 subcellular localization that have the potential to regulate ZnT3 zinc transport function. In this proposal, we will specifically explore these novel regulatory paradigms testing the hypothesis that endosome-specific zinc transporter interactions regulate zinc transporter activity and resistance to metal-induced cytotoxicity.