Role of Copper in LPS-mediated microglial activation

摘要： 小胶质细胞对维持中枢神经系统(CNS)的内部环境至关重要。这些 特化的驻留细胞的功能是滋养和支持神经元，并作为 对神经元损伤的反应。作为对神经病理状态的反应，静止的小胶质细胞经历了一系列 导致前炎性和细胞毒性介质的释放以清除病原体的变化。 在通过吞噬和/或清除毒素和毒物清除受损细胞后，小胶质细胞返回到 静息状态或经历程序性细胞死亡。因此，小胶质细胞表现出不同的表型。 对周围环境的影响。适当的表型表达是成功去除的关键 以减少对周围神经细胞的损伤。慢性小胶质细胞的激活 在各种神经退行性疾病中观察到，但到目前为止，还不清楚小胶质细胞的激活是否 由于持续的神经元变性保证了它们的激活状态，或者是由于小胶质细胞功能障碍， 包括未能上调或下调包括一氧化氮在内的细胞毒性介质的释放 (否)。NO既是一种强有力的细胞毒介质，也是小胶质细胞内细胞信号的关键调节因子。我们的 假设小胶质细胞对毒素暴露的表型反应取决于 不是的。氧化还原活性过渡金属已被认为是神经退行性疾病的重要因素。 包括阿尔茨海默氏症、帕金森氏症和变形性侧索硬化症。过渡金属铜的水平为 严格的调控和偏差将通过改变细胞的氧化还原环境来改变NO信号， 尤其是关于硫醇。我建议研究铜改变铜的机制- 刺激NO信号，从而刺激小胶质细胞的表型反应。在指导阶段， 在Andrew Gow博士的实验室中，我将研究铜对表型分化的影响 在永生化的BV-2和原代小胶质细胞培养中。特别是，我将研究铜如何改变关键- 信号分子和S-亚硝化谱对急性毒素攻击的响应以及如何 铜的存在可能会干扰适应性炎症表型的采用。无党派人士 颁奖阶段将以指导阶段取得的成果为基础。在此阶段，我将 慢性铜超负荷对特定解剖脑内小胶质细胞表型变化的影响 TX-J小鼠对全身性内毒素攻击的反应。慢性铜超载的影响将 也要研究对小胶质细胞表型的影响是永久性的还是 在多余的铜被去除后，情况发生了逆转。

Abstract: Microglia are critical to maintaining the internal environment of the central nervous system (CNS). These specialized resident cells function to nourish and support neurons and to act as a first line of defense in response to neuronal injury. In response to a neuropathological state, quiescent microglia undergo a series of changes that result in the release of proinflammatory and cytotoxic mediators for the removal of the pathogen. Upon clearance of injured cells by phagocytosis and/or the removal of toxin and toxicants, microglia return to a resting state or undergo programmed cell death. Microglia, therefore, exhibit different phenotypes depending on their surrounding environment. Expression of the appropriate phenotype is critical to the successful removal of the pathogen and to limiting damage to surrounding neurons. Chronic microglial activation has been observed in a variety of neurodegenerative diseases but, to date, it is not clear whether microglial activation is due to a persistent neuronal degeneration that warrants their activated state, or to microglial dysfunction, including a failure to either upregulate or downregulate the release of cytotoxic mediators including nitric oxide (NO). NOis both a potent cytotoxic mediator and a key regulator of cellular signaling within microglia. Our hypothesis is that the phenotypic response of microglia to toxin exposure is dependent on the metabolic fate of NO. Redox active transition metals have been proposed as important factors in neurodegenerative diseases including Alzheimer's, Parkinson's and amiotropic lateral sclerosis. Levels of the transition metal copper are strictly regulated and deviations will alter NO signaling by changing the redox environment of the cell, particularly in reference to thiols. I propose to investigate the mechanisms by which copper alters copper- stimulated NO signaling and, thus, the phenotypic response of microglia. During the mentored phase of the award in the laboratory of Dr. Andrew Gow, I will investigate the effects of copper on phenotypic differentiation in immortalized BV-2 and in primary microglia cell cultures. In particular, I will examine how copper alters key- signaling molecules and the S-nitrosylation profile in response to an acute toxin challenge and how the presence of copper might interfere with the adoption of an adaptive inflammatory phenotype. The independent phase of the award will build upon the findings obtained during the mentored phase. During this phase I will investigate the effects of chronic copper overload on microglia phenotypic changes in specific anatomical brain structures in response to systemic LPS challenge in the tx j mouse. The effects of chronic copper overload will also be investigated with respect to whether the effects on microglia phenotype are permanent or can be reversed after excess copper has been removed.