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阿尔茨海默病的病理生物学

The pathobiology of Alzheimer's disease.

作者信息

Glenner G G

机构信息

Department of Pathology, School of Medicine, University of California, San Diego, La Jolla 92093.

出版信息

Annu Rev Med. 1989;40:45-51. doi: 10.1146/annurev.me.40.020189.000401.

Abstract

The discovery of beta protein, the major component of the amyloid fibrils of the plaques and cerebral vessels and of the paired helical filaments of the neurofibrillary tangles, has provided a means to decipher the pathogenesis of Alzheimer's disease. The same lesions in aged Down's syndrome individuals have also been shown to be composed of beta protein. Gene probes localize the gene for beta protein, as well as that for familial Alzheimer's disease, to chromosome 21, but these genes are not linked. A study of posttranslational modifications of the 695-amino-acid beta-protein gene precursor, with specific reference to abnormal proteolysis, may provide insights into the cause of the amyloidotic lesions of Alzheimer's disease and the means of arresting them.

摘要

β蛋白是斑块和脑血管淀粉样纤维以及神经原纤维缠结的双螺旋丝的主要成分,其发现为解读阿尔茨海默病的发病机制提供了一种方法。老年唐氏综合征患者的相同病变也已被证明由β蛋白组成。基因探针将β蛋白基因以及家族性阿尔茨海默病基因定位到21号染色体,但这些基因没有连锁关系。对695个氨基酸的β蛋白基因前体的翻译后修饰进行研究,特别是针对异常蛋白水解,可能会为阿尔茨海默病淀粉样病变的病因及阻止病变的方法提供见解。

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