A reduced astrocyte response to β-amyloid plaques in the ageing brain associates with cognitive impairment.

β-amyloid (Aβ) plaques are a key feature of Alzheimer's disease pathology but correlate poorly with dementia. They are associated with astrocytes which may modulate the effect of Aβ-deposition on the neuropil. This study characterised the astrocyte response to Aβ plaque subtypes, and investigat...

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Main Authors: Ryan Mathur, Paul G Ince, Thais Minett, Claire J Garwood, Pamela J Shaw, Fiona E Matthews, Carol Brayne, Julie E Simpson, Stephen B Wharton, MRC Cognitive Function and Ageing Neuropathology Study Group
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4338046?pdf=render
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spelling doaj-6ec63446a247480ebbd1af8fd054f6952020-11-25T00:08:48ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01102e011846310.1371/journal.pone.0118463A reduced astrocyte response to β-amyloid plaques in the ageing brain associates with cognitive impairment.Ryan MathurPaul G InceThais MinettClaire J GarwoodPamela J ShawFiona E MatthewsCarol BrayneJulie E SimpsonStephen B WhartonMRC Cognitive Function and Ageing Neuropathology Study Groupβ-amyloid (Aβ) plaques are a key feature of Alzheimer's disease pathology but correlate poorly with dementia. They are associated with astrocytes which may modulate the effect of Aβ-deposition on the neuropil. This study characterised the astrocyte response to Aβ plaque subtypes, and investigated their association with cognitive impairment.Aβ plaque subtypes were identified in the cingulate gyrus using dual labelling immunohistochemistry to Aβ and GFAP+ astrocytes, and quantitated in two cortical areas: the area of densest plaque burden and the deep cortex near the white matter border (layer VI). Three subtypes were defined for both diffuse and compact plaques (also known as classical or core-plaques): Aβ plaque with (1) no associated astrocytes, (2) focal astrogliosis or (3) circumferential astrogliosis.In the area of densest burden, diffuse plaques with no astrogliosis (β = -0.05, p = 0.001) and with focal astrogliosis (β = -0.27, p = 0.009) significantly associated with lower MMSE scores when controlling for sex and age at death. In the deep cortex (layer VI), both diffuse and compact plaques without astrogliosis associated with lower MMSE scores (β = -0.15, p = 0.017 and β = -0.81, p = 0.03, respectively). Diffuse plaques with no astrogliosis in layer VI related to dementia status (OR = 1.05, p = 0.025). In the area of densest burden, diffuse plaques with no astrogliosis or with focal astrogliosis associated with increasing Braak stage (β = 0.01, p<0.001 and β = 0.07, p<0.001, respectively), and ApoEε4 genotype (OR = 1.02, p = 0.001 and OR = 1.10, p = 0.016, respectively). In layer VI all plaque subtypes associated with Braak stage, and compact amyloid plaques with little and no associated astrogliosis associated with ApoEε4 genotype (OR = 1.50, p = 0.014 and OR = 0.10, p = 0.003, respectively).Reactive astrocytes in close proximity to either diffuse or compact plaques may have a neuroprotective role in the ageing brain, and possession of at least one copy of the ApoEε4 allele impacts the astroglial response to Aβ plaques.http://europepmc.org/articles/PMC4338046?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ryan Mathur
Paul G Ince
Thais Minett
Claire J Garwood
Pamela J Shaw
Fiona E Matthews
Carol Brayne
Julie E Simpson
Stephen B Wharton
MRC Cognitive Function and Ageing Neuropathology Study Group
spellingShingle Ryan Mathur
Paul G Ince
Thais Minett
Claire J Garwood
Pamela J Shaw
Fiona E Matthews
Carol Brayne
Julie E Simpson
Stephen B Wharton
MRC Cognitive Function and Ageing Neuropathology Study Group
A reduced astrocyte response to β-amyloid plaques in the ageing brain associates with cognitive impairment.
PLoS ONE
author_facet Ryan Mathur
Paul G Ince
Thais Minett
Claire J Garwood
Pamela J Shaw
Fiona E Matthews
Carol Brayne
Julie E Simpson
Stephen B Wharton
MRC Cognitive Function and Ageing Neuropathology Study Group
author_sort Ryan Mathur
title A reduced astrocyte response to β-amyloid plaques in the ageing brain associates with cognitive impairment.
title_short A reduced astrocyte response to β-amyloid plaques in the ageing brain associates with cognitive impairment.
title_full A reduced astrocyte response to β-amyloid plaques in the ageing brain associates with cognitive impairment.
title_fullStr A reduced astrocyte response to β-amyloid plaques in the ageing brain associates with cognitive impairment.
title_full_unstemmed A reduced astrocyte response to β-amyloid plaques in the ageing brain associates with cognitive impairment.
title_sort reduced astrocyte response to β-amyloid plaques in the ageing brain associates with cognitive impairment.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description β-amyloid (Aβ) plaques are a key feature of Alzheimer's disease pathology but correlate poorly with dementia. They are associated with astrocytes which may modulate the effect of Aβ-deposition on the neuropil. This study characterised the astrocyte response to Aβ plaque subtypes, and investigated their association with cognitive impairment.Aβ plaque subtypes were identified in the cingulate gyrus using dual labelling immunohistochemistry to Aβ and GFAP+ astrocytes, and quantitated in two cortical areas: the area of densest plaque burden and the deep cortex near the white matter border (layer VI). Three subtypes were defined for both diffuse and compact plaques (also known as classical or core-plaques): Aβ plaque with (1) no associated astrocytes, (2) focal astrogliosis or (3) circumferential astrogliosis.In the area of densest burden, diffuse plaques with no astrogliosis (β = -0.05, p = 0.001) and with focal astrogliosis (β = -0.27, p = 0.009) significantly associated with lower MMSE scores when controlling for sex and age at death. In the deep cortex (layer VI), both diffuse and compact plaques without astrogliosis associated with lower MMSE scores (β = -0.15, p = 0.017 and β = -0.81, p = 0.03, respectively). Diffuse plaques with no astrogliosis in layer VI related to dementia status (OR = 1.05, p = 0.025). In the area of densest burden, diffuse plaques with no astrogliosis or with focal astrogliosis associated with increasing Braak stage (β = 0.01, p<0.001 and β = 0.07, p<0.001, respectively), and ApoEε4 genotype (OR = 1.02, p = 0.001 and OR = 1.10, p = 0.016, respectively). In layer VI all plaque subtypes associated with Braak stage, and compact amyloid plaques with little and no associated astrogliosis associated with ApoEε4 genotype (OR = 1.50, p = 0.014 and OR = 0.10, p = 0.003, respectively).Reactive astrocytes in close proximity to either diffuse or compact plaques may have a neuroprotective role in the ageing brain, and possession of at least one copy of the ApoEε4 allele impacts the astroglial response to Aβ plaques.
url http://europepmc.org/articles/PMC4338046?pdf=render
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