Udaka F, Kameyama M, Tomonaga M
Acta Neuropathol. 1986;70(3-4):289-95. doi: 10.1007/BF00686086.
A morphological study using a modified Golgi impregnation technique was carried out on Betz cells in the motor area of eight patients with motor neuron disease (MND) and age-matched controls without abnormal neuropathological findings during routine examination. Betz cells were categorized as normal (type I), or those with moderate (type II) or marked (type III) degeneration of dendrites. Types II and III Betz cells tended to be dominant in the cases of MND, whereas type I Betz cells constituted the highest percentage in most of the control cases. The frequently observed morphological alterations of Betz cells in MND were accumulation of lipofuscin, degeneration or loss of dendrites, and reactive astrocytic gliosis around the Betz cell soma. It was suggested that Betz cell changes in MND are not only due to aging but also to evident pathological processes, since the above-mentioned findings were more extensive in the MND cases than in the control cases. Also, the so-called lower motor neuron disease belongs to one basic disease termed "motor neuron disease", because the pathological changes of Betz cells were observed even in cases of spinal progressive muscular atrophy alone or associated with progressive bulbar palsy, which are devoid of pyramidal tract degeneration and signs of upper motor neuron lesion.
运用改良的高尔基染色技术,对8例运动神经元病(MND)患者运动区的贝茨细胞进行了形态学研究,并与年龄匹配、常规检查无异常神经病理学发现的对照组进行对比。贝茨细胞被分为正常(I型),或树突有中度(II型)或显著(III型)退变的细胞。II型和III型贝茨细胞在MND病例中往往占主导,而I型贝茨细胞在大多数对照病例中所占比例最高。MND中贝茨细胞常见的形态学改变为脂褐素积聚、树突退变或缺失,以及贝茨细胞胞体周围反应性星形胶质细胞增生。提示MND中贝茨细胞的变化不仅归因于衰老,还存在明显的病理过程,因为上述改变在MND病例中比对照病例更为广泛。此外,所谓的下运动神经元病属于一种名为“运动神经元病”的基本疾病,因为即使在单独的脊髓性进行性肌萎缩病例或合并进行性延髓麻痹的病例中也观察到了贝茨细胞的病理变化,这些病例没有锥体束退变和上运动神经元病变的体征。