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Neurobiology of Disease
Article . 2007 . Peer-reviewed
License: Elsevier TDM
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Neurobiology of Disease
Article . 2007
Data sources: DOAJ
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Analysis of alteration of p75NTR processing and signalling by PS2 mutation and γ-secretase inhibition

Authors: Ito, Yoshio; Ishii, Azusa; Passmore, A Peter; McIlroy, Stephen P;

Analysis of alteration of p75NTR processing and signalling by PS2 mutation and γ-secretase inhibition

Abstract

The presenilins (PSs) were identified as causative genes in cases of early-onset familial Alzheimer's disease (AD) and current evidence indicates that PSs are part of the gamma-secretase complex responsible for proteolytic processing of type I membrane proteins. p75NTR, a common neurotrophin receptor, was shown to be subject to gamma-secretase processing. However, it is not clear if the p75NTR downstream signal is altered in response to gamma-secretase cleavage, and further there is a possibility that AD-related PS mutations may affect this cleavage, resulting in pathogenic alterations in signal transduction. In this study, we confirmed that p75NTR downstream signalling is altered by PS2 mutation or gamma-secretase inhibition in SHSY-5Y cells. The activity of the small GTPase RhoA is strongly affected by these treatments. This study demonstrates that gamma-secretase and PS2 play an important role in regulating neurotrophin signal transduction and either mutation of PS2 or inhibition of gamma-secretase disturbs this function.

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Keywords

TNF Receptor-Associated Factor 4, name=Neurology, TrkA, Immunoblotting, 610, RhoA, Neurosciences. Biological psychiatry. Neuropsychiatry, /dk/atira/pure/subjectarea/asjc/2800/2808, Receptor, Nerve Growth Factor, Presenilin, p75NTR, Neurotrophin pathway, Cell Line, Tumor, Mutation, Presenilin-2, Humans, Amyloid Precursor Protein Secretases, rhoA GTP-Binding Protein, Alzheimer’s disease, RC321-571, Signal Transduction

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    3
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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    influence
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
3
Average
Average
Average
gold