Abstract

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-β (Aβ) 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 Aβ and other amyloid proteins.

Highlights

  • Alzheimer disease (AD)3 is the most common form of elderly dementia

  • The amyloid cascade hypothesis suggests that deposition of A␤ aggregates in brain plays a vital role in AD development [4]

  • Two recent reviews [7, 8] respectively reject and support the amyloid cascade hypothesis, they both agree on one point: AD progression is tightly connected to A␤ aggregation, several other factors likely contribute to the development of AD

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Summary

MINIREVIEW crossmark

Cross-interactions between the Alzheimer Disease Amyloid-␤ Peptide and Other Amyloid Proteins: A Further Aspect of the Amyloid Cascade Hypothesis*. 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. Missense mutations in the A␤PP, apoE, PS1, and PS2 genes can increase accumulation and toxicity of A␤ aggregates, and the “on-pathway” intermediate aggregates seem to be the most cell-damaging species [6] This provides strong support for the amyloid cascade hypothesis, which remains disputed. A␤42 affects PrP biological activity because prion binding and prion-dependent inhibition of long-term potentiation are regulated by the presence of A␤ protofibrils These aggregates have a linear structure, stronger binding. Associations between amyloid proteins and certain diseases, according to current understanding

Dialysis related amyloidosis ϫ
Apolipoprotein AI
Cystatin C
Serum Amyloid P Component and Fibrinogen
Other Amyloid Proteins
Findings
ADDITIONS AND CORRECTIONS
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