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肌萎缩侧索硬化症中的布尼亚小体。

Bunina bodies in amyotrophic lateral sclerosis.

作者信息

Okamoto Koichi, Mizuno Yuji, Fujita Yukio

机构信息

Department of Neurology, Gunma University Graduate School of Medicine, Gunma, Japan.

出版信息

Neuropathology. 2008 Apr;28(2):109-15. doi: 10.1111/j.1440-1789.2007.00873.x. Epub 2007 Dec 5.

Abstract

Bunina bodies, which are small eosinophilic intraneuronal inclusions in the remaining lower motor neurons, are generally considered to be a specific pathologic hallmark of amyotrophic lateral sclerosis (ALS). One year before a publication by Bunina, van Reeth et al. described similar intracytoplasmic inclusions in the anterior horn cells in a patient with Pick's dementia with atypical ALS. At present, only two proteins have been shown to be present in Bunina bodies, one is cystatin C and the other is transferrin. Bunina bodies consist of amorphous electron-dense material surrounded by tubular and vesicular structures on electron microscopy. Although the nature and significance of Bunina bodies in ALS are not yet clear, the bodies may be abnormal accumulations of unknown proteinous materials.

摘要

布尼纳小体是剩余下运动神经元内的嗜酸性神经元内包涵体,通常被认为是肌萎缩侧索硬化症(ALS)的一种特异性病理标志。在布尼纳发表相关文章的前一年,范·里特等人描述了一名患有皮克痴呆伴非典型ALS患者的前角细胞中存在类似的胞质内包涵体。目前,已证实布尼纳小体中仅存在两种蛋白质,一种是胱抑素C,另一种是转铁蛋白。在电子显微镜下,布尼纳小体由无定形电子致密物质组成,周围环绕着管状和囊泡状结构。尽管布尼纳小体在ALS中的性质和意义尚不清楚,但这些小体可能是未知蛋白质物质的异常积聚。

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