Cross-interactions between the Alzheimer Disease Amyloid-β Peptide and Other Amyloid Proteins: A Further Aspect of the Amyloid Cascade Hypothesis

被引:118
作者
Luo, Jinghui [1 ]
Warmlander, Sebastian K. T. S. [2 ]
Graslund, Astrid [2 ]
Abrahams, Jan Pieter [3 ,4 ]
机构
[1] Univ Oxford, Chem Res Lab, Oxford OX1 3TA, England
[2] Stockholm Univ, Dept Biochem & Biophys, SE-10691 Stockholm, Sweden
[3] Univ Basel, Biozentrum, CH-4056 Basel, Switzerland
[4] Paul Scherrer Inst, Lab Biomol Res, CH-5232 Villigen, Switzerland
关键词
A-BETA; ALPHA-SYNUCLEIN; CYSTATIN-C; PRION PROTEIN; PRECURSOR PROTEIN; P COMPONENT; MOUSE MODEL; NEURONAL DEFICITS; DIABETES-MELLITUS; BINDING-SITES;
D O I
10.1074/jbc.R116.714576
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Many protein folding diseases are intimately associated with accumulation of amyloid aggregates. The amyloid materials formed by different proteins/peptides share many structural similarities, despite sometimes large amino acid sequence differences. Some amyloid diseases constitute risk factors for others, and the progression of one amyloid disease may affect the progression of another. These connections are arguably related to amyloid aggregates of one protein being able to directly nucleate amyloid formation of another, different protein: the amyloid cross-interaction. Here, we discuss such cross-interactions between the Alzheimer disease amyloid-beta (A beta) peptide and other amyloid proteins in the context of what is known from in vitro and in vivo experiments, and of what might be learned from clinical studies. The aim is to clarify potential molecular associations between different amyloid diseases. We argue that the amyloid cascade hypothesis in Alzheimer disease should be expanded to include cross-interactions between A beta and other amyloid proteins.
引用
收藏
页码:16485 / 16493
页数:9
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