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散发性运动神经元病中的神经元包涵体α-突触核蛋白检测呈阴性。

Neuronal inclusions in sporadic motor neuron disease are negative for alpha-synuclein.

作者信息

Sasaki Shoichi, Komori Takashi, Iwata Makoto

机构信息

Department of Neurology, Neurological Institute, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo 162-8666, Japan.

出版信息

Neurosci Lett. 2006;397(1-2):15-9. doi: 10.1016/j.neulet.2005.11.056. Epub 2006 Jan 6.

Abstract

Alpha-synuclein has been implicated in neurodegenerative diseases characterized by Lewy bodies. However, we have only scanty information on the immunoreactivity of alpha-synuclein in other inclusion bodies such as the Lewy body-like inclusions and the skein-like inclusions observed in motor neuron disease (MND). In this report, we immunocytochemically investigated inclusion bodies observed in the anterior horn neurons of the spinal cord in 29 patients with sporadic MND. Sixteen age-matched patients without any neurological disease served as controls. In MND patients, we recognized Lewy body-like hyaline inclusions, skein-like inclusions, Bunina bodies, basophilic inclusions, and intracytoplasmic hyaline (colloid) inclusions, but none of them were immunostained for alpha-synuclein. Our findings in this study do not support the hypothesis that MND could be classified as one of the diseases grouped as alpha-synucleinopathies.

摘要

α-突触核蛋白与以路易小体为特征的神经退行性疾病有关。然而,关于α-突触核蛋白在其他包涵体中的免疫反应性,如在运动神经元病(MND)中观察到的路易小体样包涵体和丝状包涵体,我们所知甚少。在本报告中,我们采用免疫细胞化学方法研究了29例散发性MND患者脊髓前角神经元中观察到的包涵体。16例年龄匹配的无任何神经疾病的患者作为对照。在MND患者中,我们识别出路易小体样透明包涵体、丝状包涵体、布尼纳小体、嗜碱性包涵体和胞质内透明(胶体)包涵体,但它们均未被α-突触核蛋白免疫染色。我们在本研究中的发现不支持MND可被归类为α-突触核蛋白病之一的假说。

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