iTRAQ analysis of complex proteome alterations in 3xTgAD Alzheimer's mice: understanding the interface between physiology and disease.

Alzheimer's disease (AD) is characterized by progressive cognitive impairment associated with accumulation of amyloid beta-peptide, synaptic degeneration and the death of neurons in the hippocampus, and temporal, parietal and frontal lobes of the cerebral cortex. Analysis of postmortem brain ti...

Full description

Bibliographic Details
Main Authors: Bronwen Martin, Randall Brenneman, Kevin G Becker, Marjan Gucek, Robert N Cole, Stuart Maudsley
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-07-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2453232?pdf=render
_version_ 1818542030724268032
author Bronwen Martin
Randall Brenneman
Kevin G Becker
Marjan Gucek
Robert N Cole
Stuart Maudsley
author_facet Bronwen Martin
Randall Brenneman
Kevin G Becker
Marjan Gucek
Robert N Cole
Stuart Maudsley
author_sort Bronwen Martin
collection DOAJ
description Alzheimer's disease (AD) is characterized by progressive cognitive impairment associated with accumulation of amyloid beta-peptide, synaptic degeneration and the death of neurons in the hippocampus, and temporal, parietal and frontal lobes of the cerebral cortex. Analysis of postmortem brain tissue from AD patients can provide information on molecular alterations present at the end of the disease process, but cannot discriminate between changes that are specifically involved in AD versus those that are simply a consequence of neuronal degeneration. Animal models of AD provide the opportunity to elucidate the molecular changes that occur in brain cells as the disease process is initiated and progresses. To this end, we used the 3xTgAD mouse model of AD to gain insight into the complex alterations in proteins that occur in the hippocampus and cortex in AD. The 3xTgAD mice express mutant presenilin-1, amyloid precursor protein and tau, and exhibit AD-like amyloid and tau pathology in the hippocampus and cortex, and associated cognitive impairment. Using the iTRAQ stable-isotope-based quantitative proteomic technique, we performed an in-depth proteomic analysis of hippocampal and cortical tissue from 16 month old 3xTgAD and non-transgenic control mice. We found that the most important groups of significantly altered proteins included those involved in synaptic plasticity, neurite outgrowth and microtubule dynamics. Our findings have elucidated some of the complex proteome changes that occur in a mouse model of AD, which could potentially illuminate novel therapeutic avenues for the treatment of AD and other neurodegenerative disorders.
first_indexed 2024-12-11T22:16:50Z
format Article
id doaj.art-f77601e35d24480fb245a7547a90d2f5
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-12-11T22:16:50Z
publishDate 2008-07-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-f77601e35d24480fb245a7547a90d2f52022-12-22T00:48:35ZengPublic Library of Science (PLoS)PLoS ONE1932-62032008-07-0137e275010.1371/journal.pone.0002750iTRAQ analysis of complex proteome alterations in 3xTgAD Alzheimer's mice: understanding the interface between physiology and disease.Bronwen MartinRandall BrennemanKevin G BeckerMarjan GucekRobert N ColeStuart MaudsleyAlzheimer's disease (AD) is characterized by progressive cognitive impairment associated with accumulation of amyloid beta-peptide, synaptic degeneration and the death of neurons in the hippocampus, and temporal, parietal and frontal lobes of the cerebral cortex. Analysis of postmortem brain tissue from AD patients can provide information on molecular alterations present at the end of the disease process, but cannot discriminate between changes that are specifically involved in AD versus those that are simply a consequence of neuronal degeneration. Animal models of AD provide the opportunity to elucidate the molecular changes that occur in brain cells as the disease process is initiated and progresses. To this end, we used the 3xTgAD mouse model of AD to gain insight into the complex alterations in proteins that occur in the hippocampus and cortex in AD. The 3xTgAD mice express mutant presenilin-1, amyloid precursor protein and tau, and exhibit AD-like amyloid and tau pathology in the hippocampus and cortex, and associated cognitive impairment. Using the iTRAQ stable-isotope-based quantitative proteomic technique, we performed an in-depth proteomic analysis of hippocampal and cortical tissue from 16 month old 3xTgAD and non-transgenic control mice. We found that the most important groups of significantly altered proteins included those involved in synaptic plasticity, neurite outgrowth and microtubule dynamics. Our findings have elucidated some of the complex proteome changes that occur in a mouse model of AD, which could potentially illuminate novel therapeutic avenues for the treatment of AD and other neurodegenerative disorders.http://europepmc.org/articles/PMC2453232?pdf=render
spellingShingle Bronwen Martin
Randall Brenneman
Kevin G Becker
Marjan Gucek
Robert N Cole
Stuart Maudsley
iTRAQ analysis of complex proteome alterations in 3xTgAD Alzheimer's mice: understanding the interface between physiology and disease.
PLoS ONE
title iTRAQ analysis of complex proteome alterations in 3xTgAD Alzheimer's mice: understanding the interface between physiology and disease.
title_full iTRAQ analysis of complex proteome alterations in 3xTgAD Alzheimer's mice: understanding the interface between physiology and disease.
title_fullStr iTRAQ analysis of complex proteome alterations in 3xTgAD Alzheimer's mice: understanding the interface between physiology and disease.
title_full_unstemmed iTRAQ analysis of complex proteome alterations in 3xTgAD Alzheimer's mice: understanding the interface between physiology and disease.
title_short iTRAQ analysis of complex proteome alterations in 3xTgAD Alzheimer's mice: understanding the interface between physiology and disease.
title_sort itraq analysis of complex proteome alterations in 3xtgad alzheimer s mice understanding the interface between physiology and disease
url http://europepmc.org/articles/PMC2453232?pdf=render
work_keys_str_mv AT bronwenmartin itraqanalysisofcomplexproteomealterationsin3xtgadalzheimersmiceunderstandingtheinterfacebetweenphysiologyanddisease
AT randallbrenneman itraqanalysisofcomplexproteomealterationsin3xtgadalzheimersmiceunderstandingtheinterfacebetweenphysiologyanddisease
AT kevingbecker itraqanalysisofcomplexproteomealterationsin3xtgadalzheimersmiceunderstandingtheinterfacebetweenphysiologyanddisease
AT marjangucek itraqanalysisofcomplexproteomealterationsin3xtgadalzheimersmiceunderstandingtheinterfacebetweenphysiologyanddisease
AT robertncole itraqanalysisofcomplexproteomealterationsin3xtgadalzheimersmiceunderstandingtheinterfacebetweenphysiologyanddisease
AT stuartmaudsley itraqanalysisofcomplexproteomealterationsin3xtgadalzheimersmiceunderstandingtheinterfacebetweenphysiologyanddisease