Journal
BIOCHEMICAL JOURNAL
Volume 391, Issue -, Pages 59-67Publisher
PORTLAND PRESS LTD
DOI: 10.1042/BJ20050700
Keywords
aging; Alzheimer's disease; amyloid precursor protein; ceramide; p75(NTR) (p75 neurotrophin receptor); neurotrophin
Categories
Funding
- NINDS NIH HHS [NS045669, R01 NS045669] Funding Source: Medline
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Aging is the single most important risk factor for AD (Alzheimer's disease). However, the molecular events that connect normal aging to AD are mostly unknown. The abnormal accumulation of A beta (amyloid P-peptide) in the form of senile plaques is one of the main characteristics of AD. In the present study, we show that two members of the neurotrophin receptor superfamily, TrkA (tyrosine kinase receptor A) and p75(NTR) (p75 neurotrophin receptor), differentially regulate the processing of APP (amyloid precursor protein): TrkA reduces, whereas p75(NTR) activates, beta-cleavage of APP. The p75(NTR)-dependent effect requires NGF (nerve growth factor) binding and activation of the second messenger ceramide. We also show that normal aging activates A beta generation in the brain by 'switching' from the TrkA to the p75(NTR) receptor system. Such an effect is abolished in p75(NTR) 'knockout' animals, and can be blocked by both caloric restriction and inhibitors of nSMase (neutral sphingomyelinase). In contrast with caloric restriction, which prevents the age-associated up-regulation of p75(NTR) expression, nSMase inhibitors block the activation of ceramide. When taken together, these results indicate that the p75(NTR_) ceramide signalling pathway activates the rate of A beta generation in an age-dependent fashion, and provide a new target for both the understanding and the prevention of late-onset AD.
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