Genoud Sian, Roberts Blaine R, Gunn Adam P, Halliday Glenda M, Lewis Simon J G, Ball Helen J, Hare Dominic J, Double Kay L
Discipline of Biomedical Science and Brain and Mind Centre, Sydney Medical School, The University of Sydney, Camperdown, NSW 2006, Australia.
The Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, VIC 3052, Australia.
Metallomics. 2017 Oct 18;9(10):1447-1455. doi: 10.1039/c7mt00244k.
Elevated iron and decreased copper levels are cardinal features of the degenerating substantia nigra pars compacta in the Parkinson's disease brain. Both of these redox-active metals, and fellow transition metals manganese and zinc, are found at high concentrations within the midbrain and participate in a range of unique biological reactions. We examined the total metal content and cellular compartmentalisation of manganese, iron, copper and zinc in the degenerating substantia nigra, disease-affected but non-degenerating fusiform gyrus, and unaffected occipital cortex in the post mortem Parkinson's disease brain compared with age-matched controls. An expected increase in iron and a decrease in copper concentration was isolated to the soluble cellular fraction, encompassing both interstitial and cytosolic metals and metal-binding proteins, rather than the membrane-associated or insoluble fractions. Manganese and zinc levels did not differ between experimental groups. Altered Fe and Cu levels were unrelated to Braak pathological staging in our cases of late-stage (Braak stage V and VI) disease. The data supports our hypothesis that regional alterations in Fe and Cu, and in proteins that utilise these metals, contribute to the regional selectively of neuronal vulnerability in this disorder.
铁含量升高和铜含量降低是帕金森病患者大脑中黑质致密部退化的主要特征。这两种具有氧化还原活性的金属,以及同为过渡金属的锰和锌,在中脑内的浓度很高,并参与一系列独特的生物反应。我们研究了帕金森病患者死后大脑中退化的黑质、受疾病影响但未退化的梭状回以及未受影响的枕叶皮质中锰、铁、铜和锌的总金属含量及细胞区室化情况,并与年龄匹配的对照组进行了比较。铁含量的预期增加和铜浓度的降低被分离到可溶性细胞组分中,该组分包括细胞间质和胞质中的金属及金属结合蛋白,而非膜相关或不溶性组分。实验组之间锰和锌的水平没有差异。在我们的晚期(Braak V期和VI期)病例中,铁和铜水平的改变与Braak病理分期无关。这些数据支持了我们的假设,即铁和铜以及利用这些金属的蛋白质的区域改变,导致了该疾病中神经元易损性的区域选择性。