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转甲状腺素蛋白可隔离β淀粉样蛋白并防止淀粉样蛋白形成。

Transthyretin sequesters amyloid beta protein and prevents amyloid formation.

作者信息

Schwarzman A L, Gregori L, Vitek M P, Lyubski S, Strittmatter W J, Enghilde J J, Bhasin R, Silverman J, Weisgraber K H, Coyle P K

机构信息

Department of Psychiatry, School of Medicine, State University of New York at Stony Brook 11794.

出版信息

Proc Natl Acad Sci U S A. 1994 Aug 30;91(18):8368-72. doi: 10.1073/pnas.91.18.8368.

Abstract

The cardinal pathological features of Alzheimer disease are depositions of aggregated amyloid beta protein (A beta) in the brain and cerebrovasculature. However, the A beta is found in a soluble form in cerebrospinal fluid in healthy individuals and patients with Alzheimer disease. We postulate that sequestration of A beta precludes amyloid formation. Failure to sequester A beta in Alzheimer disease may result in amyloidosis. When we added A beta to cerebrospinal fluid of patients and controls it was rapidly sequestered into stable complexes with transthyretin. Complexes with apolipoprotein E, which has been shown to bind A beta in vitro, were not observed in cerebrospinal fluid. Additional in vitro studies showed that both purified transthyretin and apolipoprotein E prevent amyloid formation.

摘要

阿尔茨海默病的主要病理特征是大脑和脑血管系统中聚集的β淀粉样蛋白(Aβ)沉积。然而,在健康个体和阿尔茨海默病患者的脑脊液中,Aβ以可溶形式存在。我们推测,Aβ的隔离可防止淀粉样蛋白形成。在阿尔茨海默病中未能隔离Aβ可能导致淀粉样变性。当我们将Aβ添加到患者和对照组的脑脊液中时,它会迅速与转甲状腺素蛋白结合形成稳定的复合物。在脑脊液中未观察到与已证明在体外能结合Aβ的载脂蛋白E形成的复合物。额外的体外研究表明,纯化的转甲状腺素蛋白和载脂蛋白E均可防止淀粉样蛋白形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33d8/44607/6410da844339/pnas01140-0071-a.jpg

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