Wegiel J, Wisniewski H M
Department of Pathological Neurobiology, New York State Institute for Basic Research in Developmental Disabilities, Staten Island 10314.
Acta Neuropathol. 1994;87(4):355-61. doi: 10.1007/BF00313604.
Ultrastructural study of the cerebral cortex of nine brains of individuals with Alzheimer's disease (AD) revealed four types of pathological changes of astrocytes. Rosenthal fibers were found in three cases, eosinophilic inclusions in one, anchoraged densities with desmosome-like structures in two, and corpora amylacea in four. In two biopsies, Rosenthal fibers were seen in less than 5% astrocytes, but in a third biopsy with numerous plaques, tangles, and severe neuronal loss, they were present in about 40% of astrocytes. In one case with severe AD pathology and numerous Rosenthal fibers, the cytoplasm of some astrocytes was occupied by inclusions composed of electron-dense granules 3-6 microns in diameter or aggregates of inclusions greater than 12 microns in diameter. Ultrastructurally, they were similar to eosinophilic inclusions observed in Aicardi syndrome and brain malformations. The presence of eosinophilic inclusions in the brain of elderly persons with Alzheimer's disease does not confirm the previous suggestion that this form of astrocyte pathology is typical for protoplasmic astrocytes and developmental brain malformations. Development anchorage densities associated with hemidesmosome-like structures, which reinforce astrocyte cell membranes facing the perivascular space, may reflect adaptation of astrocytes to the complex of changes that occurs in atrophic brain. Morphological changes in astrocytes in areas with numerous plaques and massive infiltration of intercellular space with beta-amyloid fibrils and remnants of neurons and ghost tangles suggest that astrocyte pathology is a late unspecific reaction to the cascade of changes induced by beta-amyloid deposition that causes neuronal degeneration and brain atrophy.
对9例阿尔茨海默病(AD)患者大脑皮质进行的超微结构研究揭示了星形胶质细胞的四种病理变化类型。在3例中发现了罗森塔尔纤维,1例中有嗜酸性包涵体,2例中有具有桥粒样结构的附着密度,4例中有淀粉样小体。在两份活检标本中,罗森塔尔纤维见于不到5%的星形胶质细胞中,但在第三份活检标本中有大量斑块、缠结和严重神经元丢失,它们存在于约40%的星形胶质细胞中。在1例具有严重AD病理和大量罗森塔尔纤维的病例中,一些星形胶质细胞的细胞质被由直径3 - 6微米的电子致密颗粒组成的包涵体或直径大于12微米的包涵体聚集体占据。在超微结构上,它们类似于在艾卡迪综合征和脑畸形中观察到的嗜酸性包涵体。在患有阿尔茨海默病的老年人脑中存在嗜酸性包涵体并不能证实先前的观点,即这种星形胶质细胞病理形式是原浆性星形胶质细胞和发育性脑畸形所特有的。与半桥粒样结构相关的发育性附着密度增强了面向血管周围间隙的星形胶质细胞膜,可能反映了星形胶质细胞对萎缩性脑中发生的复杂变化的适应。在有大量斑块以及细胞间空间被β - 淀粉样纤维、神经元残余物和幽灵缠结大量浸润的区域,星形胶质细胞的形态变化表明,星形胶质细胞病理是对由β - 淀粉样蛋白沉积引起的神经元变性和脑萎缩的一系列变化的晚期非特异性反应。