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[早老素作为阿尔茨海默病的标志物]

[Presenilins as a marker of Alzheimer's disease].

作者信息

Scheper W, van Gool W A

机构信息

Academisch Medisch Centrum, afd. Neurologie, Amsterdam.

出版信息

Ned Tijdschr Geneeskd. 1998 May 30;142(22):1247-52.

PMID:9749296
Abstract

Although the sporadic form of Alzheimer's disease is the most common, rare familial variants exist. Approximately 50% of these cases are caused by a mutation in the presenilin genes. Mutations in presinilin genes give rise to Alzheimer's disease in a dominant pattern of inheritance with an early age of onset (< 60 years). Both presenilins (PS-1 and PS-2) are transmembrane proteins localized in the intracellular membranes of the endoplasmatic reticulum and Golgi apparatus. This suggests they play a role in transport or sorting of proteins in the cell. Different lines of evidence directly link presenilin to the formation of beta-amyloid, an important constituent of senile plaques. PS-1 has an essential function during development: mice lacking intact PS-1 are not viable. In addition, structural and functional homologies have been identified between presenilins and Notch signal transduction pathways, which play a role in development. The discovery of the presenilin mutations has provided a new angle to Alzheimer's disease research. Eventually, this will probably greatly contribute to knowledge of the pathogenesis of the disease and in time support the development of novel therapeutic strategies.

摘要

尽管散发性阿尔茨海默病最为常见,但也存在罕见的家族性变体。这些病例中约50%是由早老素基因突变引起的。早老素基因突变以显性遗传模式导致阿尔茨海默病,发病年龄较早(<60岁)。两种早老素(PS-1和PS-2)都是跨膜蛋白,定位于内质网和高尔基体的内膜。这表明它们在细胞内蛋白质的运输或分选过程中发挥作用。不同的证据线索直接将早老素与β-淀粉样蛋白的形成联系起来,β-淀粉样蛋白是老年斑的重要组成部分。PS-1在发育过程中具有重要功能:缺乏完整PS-1的小鼠无法存活。此外,早老素与在发育中起作用的Notch信号转导途径之间已确定存在结构和功能同源性。早老素突变的发现为阿尔茨海默病研究提供了一个新视角。最终,这可能会极大地促进对该疾病发病机制的了解,并及时支持新型治疗策略的开发。

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