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肌萎缩侧索硬化症上运动神经元的免疫细胞化学和超微结构研究

Immunocytochemical and ultrastructural studies of upper motor neurons in amyotrophic lateral sclerosis.

作者信息

Murayama S, Bouldin T W, Suzuki K

机构信息

Department of Pathology (Neuropathology), University of North Carolina, Chapel Hill 27599-7525.

出版信息

Acta Neuropathol. 1992;83(5):518-24. doi: 10.1007/BF00310029.

Abstract

The pathological alterations in upper motor neurons were investigated in 27 cases of adult-onset sporadic amyotrophic lateral sclerosis (ALS). No significant cytoskeletal alterations were found in the Betz cells of any of the cases except one, although cytoskeletal pathology was consistently present in lower motor neurons. The one case had severe circumscribed atrophy of the precentral gyrus and, microscopically, had argentophilic intracytoplasmic inclusions in Betz cells and other pyramidal neurons in the primary motor area as eell as in the lower motor neurons. Immunocytochemically these inclusions contained the epitope of phosphorylated neurofilament and ubiquitin and ultrastructurally consisted of granule-associated filaments with neurofilaments. This is the first demonstration of alterations of cytoskeleton and ubiquitination in the giant cells of Betz, an established subset of upper motor neurons in ALS. Thus, although uncommon, cytoskeletal changes can be found in upper motor neurons in some ALS cases.

摘要

对27例成年起病的散发性肌萎缩侧索硬化症(ALS)患者的上运动神经元病理改变进行了研究。除1例患者外,其余病例的贝茨细胞均未发现明显的细胞骨架改变,尽管下运动神经元中始终存在细胞骨架病理改变。该病例中央前回有严重的局限性萎缩,显微镜下,在主要运动区的贝茨细胞和其他锥体神经元以及下运动神经元中可见嗜银性胞浆内包涵体。免疫细胞化学显示这些包涵体含有磷酸化神经丝和泛素的表位,超微结构由与神经丝相关的颗粒状细丝组成。这是首次证明在ALS患者中,作为上运动神经元既定亚群的贝茨巨细胞中细胞骨架和泛素化发生改变。因此,尽管不常见,但在某些ALS病例的上运动神经元中可发现细胞骨架变化。

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