Waggoner D J, Bartnikas T B, Gitlin J D
Edward Mallinckrodt Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
Neurobiol Dis. 1999 Aug;6(4):221-30. doi: 10.1006/nbdi.1999.0250.
Copper is an essential trace metal which plays a fundamental role in the biochemistry of the human nervous system. Menkes disease and Wilson disease are inherited disorders of copper metabolism and the dramatic neurodegenerative phenotypes of these two diseases underscore the essential nature of copper in nervous system development as well as the toxicity of this metal when neuronal copper homeostasis is perturbed. Ceruloplasmin contains 95% of the copper found in human plasma and inherited loss of this essential ferroxidase is associated with progressive neurodegeneration of the retina and basal ganglia. Gain-of-function mutations in the cytosolic copper enzyme superoxide dismutase result in the motor neuron degeneration of amyotrophic lateral sclerosis and current evidence suggests a direct pathogenic role for copper in this process. Recent studies have also implicated copper in the pathogenesis of neuronal injury in Alzheimer's disease and the prion-mediated encephalopathies, suggesting that further elucidation of the mechanisms of copper trafficking and metabolism within the nervous system will be of direct relevance to our understanding of the pathophysiology and treatment of neurodegenerative disease.
铜是一种必需的微量元素,在人类神经系统的生物化学过程中起着至关重要的作用。门克斯病和威尔逊病是铜代谢的遗传性疾病,这两种疾病显著的神经退行性表型突出了铜在神经系统发育中的本质特性,以及当神经元铜稳态受到干扰时这种金属的毒性。铜蓝蛋白含有人类血浆中95%的铜,这种必需铁氧化酶的遗传性缺失与视网膜和基底神经节的进行性神经退行性变有关。胞质铜酶超氧化物歧化酶的功能获得性突变导致肌萎缩侧索硬化症的运动神经元变性,目前的证据表明铜在这一过程中具有直接的致病作用。最近的研究还表明铜与阿尔茨海默病和朊病毒介导的脑病中神经元损伤的发病机制有关,这表明进一步阐明神经系统内铜转运和代谢的机制将与我们对神经退行性疾病的病理生理学和治疗的理解直接相关。