Format:
Online-Ressource
ISSN:
1757-4684
Content:
Abstract: Surrogate markers for the Alzheimer disease (AD)‐associated 42‐amino acid form of amyloid‐β (Aβ42) have been sought because they may aid in the diagnosis of AD and for clarification of disease pathogenesis. Here, we demonstrate that human cerebrospinal fluid (CSF) contains three APLP1‐derived Aβ‐like peptides (APL1β) that are generated by β‐ and γ‐cleavages at a concentration of ∼4.5 nM. These novel peptides, APL1β25, APL1β27 and APL1β28, were not deposited in AD brains. Interestingly, most γ‐secretase modulators (GSMs) and familial AD‐associated presenilin1 mutants that up‐regulate the relative production of Aβ42 cause a parallel increase in the production of APL1β28 in cultured cells. Moreover, in CSF from patients with pathological mutations in presenilin1 gene, the relative APL1β28 levels are higher than in non‐AD controls, while the relative Aβ42 levels are unchanged or lower. Most strikingly, the relative APL1β28 levels are higher in CSF from sporadic AD patients (regardless of whether they are at mild cognitive impairment or AD stage), than those of non‐AD controls. Based on these results, we propose the relative level of APL1β28 in the CSF as a candidate surrogate marker for the relative level of Aβ42 production in the brain.
In:
volume:1
In:
number:4
In:
year:2009
In:
pages:223-235
In:
extent:13
In:
European Molecular Biology Organization, EMBO molecular medicine, Weinheim : Wiley-VCH, [2009]-, 1, Heft 4 (2009), 223-235 (gesamt 13), 1757-4684
Language:
English
DOI:
10.1002/emmm.200900026
URN:
urn:nbn:de:101:1-2023041916443750811113
URL:
https://doi.org/10.1002/emmm.200900026
URL:
https://nbn-resolving.org/urn:nbn:de:101:1-2023041916443750811113
URL:
https://d-nb.info/1286649358/34
URL:
https://doi.org/10.1002/emmm.200900026
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