Duda J E, Giasson B I, Chen Q, Gur T L, Hurtig H I, Stern M B, Gollomp S M, Ischiropoulos H, Lee V M, Trojanowski J Q
Center for Neurodegenerative Disease Research and Department of Pathology and Laboratory Medicine, The University of Pennsylvania, Philadelphia, USA.
Am J Pathol. 2000 Nov;157(5):1439-45. doi: 10.1016/S0002-9440(10)64781-5.
Reactive nitrogen species may play a mechanistic role in neurodegenerative diseases by posttranslationally altering normal brain proteins. In support of this hypothesis, we demonstrate that an anti-3-nitrotyrosine polyclonal antibody stains all of the major hallmark lesions of synucleinopathies including Lewy bodies, Lewy neurites and neuraxonal spheroids in dementia with Lewy bodies, the Lewy body variant of Alzheimer's disease, and neurodegeneration with brain iron accumulation type 1, as well as glial and neuronal cytoplasmic inclusions in multiple system atrophy. This antibody predominantly recognized nitrated alpha-synuclein when compared to other in vitro nitrated constituents of these pathological lesions, such as neurofilament subunits and microtubules. Collectively, these findings imply that alpha-synuclein is nitrated in pathological lesions. The widespread presence of nitrated alpha-synuclein in diverse intracellular inclusions suggests that oxidation/nitration is involved in the onset and/or progression of neurodegenerative diseases.
活性氮物质可能通过对正常脑蛋白进行翻译后修饰,在神经退行性疾病中发挥机制性作用。为支持这一假说,我们证明一种抗3-硝基酪氨酸多克隆抗体可标记突触核蛋白病的所有主要标志性病变,包括路易体痴呆中的路易体、路易神经突和神经轴突球状体、阿尔茨海默病的路易体变异型以及1型脑铁沉积神经变性病,以及多系统萎缩中的胶质和神经元胞质内含物。与这些病理病变的其他体外硝化成分(如神经丝亚基和微管)相比,该抗体主要识别硝化的α-突触核蛋白。总体而言,这些发现表明α-突触核蛋白在病理病变中被硝化。硝化的α-突触核蛋白在多种细胞内包涵体中的广泛存在表明氧化/硝化参与了神经退行性疾病的发生和/或进展。