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通过原位DNA片段化评估阿尔茨海默病中的细胞死亡。

Cell death in Alzheimer's disease evaluated by DNA fragmentation in situ.

作者信息

Lassmann H, Bancher C, Breitschopf H, Wegiel J, Bobinski M, Jellinger K, Wisniewski H M

机构信息

Research Unit for Experimental Neuropathology, Austrian Academy of Sciences, Wien.

出版信息

Acta Neuropathol. 1995;89(1):35-41. doi: 10.1007/BF00294257.

Abstract

Loss of nerve cells is a hallmark of the pathology of Alzheimer's disease (AD), yet the patterns of cell death are unknown. By analyzing DNA fragmentation in situ we found evidence for cell death not only of nerve cells but also of oligodendrocytes and microglia in AD brains. In average, 30 times more brain cells showed DNA fragmentation in AD as compared to age-matched controls. Nuclear alterations suggestive of apoptosis were rare in degenerating cells. Even though the majority of degenerating cells were not located within amyloid deposits and did not contain neurofibrillary tangles, neurons situated within areas of amyloid deposits or affected by neurofibrillary degeneration revealed a higher risk of DNA fragmentation and death than cells not exposed to these AD changes.

摘要

神经细胞的丧失是阿尔茨海默病(AD)病理学的一个标志,但细胞死亡模式尚不清楚。通过原位分析DNA片段化,我们发现AD大脑中不仅神经细胞,而且少突胶质细胞和小胶质细胞都存在细胞死亡的证据。平均而言,与年龄匹配的对照组相比,AD大脑中显示DNA片段化的脑细胞多30倍。在退化细胞中,提示凋亡的核改变很少见。尽管大多数退化细胞并不位于淀粉样蛋白沉积物内,也不含有神经原纤维缠结,但位于淀粉样蛋白沉积物区域内或受神经原纤维变性影响的神经元,与未暴露于这些AD变化的细胞相比,显示出更高的DNA片段化和死亡风险。

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