Ko L, Sheu K F, Young O, Blass J P
Altschul Laboratory for Dementia Research, Cornell University Medical College, Burke Rehabilitation Center, White Plains, NY 10605.
Acta Neuropathol. 1990;81(1):30-40. doi: 10.1007/BF00662635.
Accumulation of paired helical filaments (PHF) in neurofibrillary tangles is a key neuropathological hallmark in Alzheimer's disease (AD). To date, PHF have been found primarily in humans. Cultured murine cholinergic neuroblastoma (S20Y) cells, following exposure to a serum-free medium or a differentiation medium, developed immunoreactivity to anti-PHF antibodies, and to the Alz-50 by immunocytochemical and immunoblot analyses. Electron microscopic examination revealed abundant fascicles of 10-nm filaments coursing tortuously amongst organelles, such as mitochondria, endoplasmic reticulum and dense-core vesicles, in perikarya and in neuritic extensions. However, subcellular structures identical or similar to PHF could not be found in these non-human cells. This convenient cell culture model may prove to be useful for studying certain aspects of the mechanisms underlying the abnormal cytoskeletal alterations which are characteristic of AD and related neurodegenerative disorders.
神经原纤维缠结中双螺旋丝(PHF)的积累是阿尔茨海默病(AD)的关键神经病理学特征。迄今为止,PHF主要在人类中发现。经免疫细胞化学和免疫印迹分析,培养的鼠胆碱能神经母细胞瘤(S20Y)细胞在暴露于无血清培养基或分化培养基后,对抗PHF抗体以及Alz-50产生免疫反应。电子显微镜检查显示,在核周体和神经突延伸部分的细胞器(如线粒体、内质网和致密核心小泡)之间,有大量10纳米细丝束蜿蜒穿过。然而,在这些非人类细胞中未发现与PHF相同或相似的亚细胞结构。这个便捷的细胞培养模型可能对研究AD及相关神经退行性疾病所特有的异常细胞骨架改变机制的某些方面有用。