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Apolipoprotein E particle size is increased in Alzheimer's disease

INTRODUCTION: Apolipoprotein E4 (apoE4) is the predominant risk factor for late-onset Alzheimer's disease (AD), but the question of which structural differences might explain its effect remains unclear. METHODS: We compared high-density lipoprotein–like apoE particles from 12 AD and 10 control...

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Autores principales: Nelson, Thomas J., Sen, Abhik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6293020/
https://www.ncbi.nlm.nih.gov/pubmed/30581971
http://dx.doi.org/10.1016/j.dadm.2018.10.005
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author Nelson, Thomas J.
Sen, Abhik
author_facet Nelson, Thomas J.
Sen, Abhik
author_sort Nelson, Thomas J.
collection PubMed
description INTRODUCTION: Apolipoprotein E4 (apoE4) is the predominant risk factor for late-onset Alzheimer's disease (AD), but the question of which structural differences might explain its effect remains unclear. METHODS: We compared high-density lipoprotein–like apoE particles from 12 AD and 10 control patients using size-exclusion chromatography. RESULTS: ApoE particles from patients genotyped as ε4/ε4 were 2.2 ± 0.3 times as massive as particles from ε3/ε3 control subjects and 1.4 ± 0.1 times as massive as particles from ε3/ε3 AD patients. The increased particle size was not because of incorporation of amyloid β or apoE proteolysis products. Particles from AD patients genotyped as ε3/ε3 were 1.59 ± 0.27 times as massive as ε3/ε3 control subjects. DISCUSSION: Increased particle size in AD is affected by APOE genotype and by disease-related differences in assembly or stability. These differences suggest that lipoprotein assembly or stability in AD brain plays an important role in determining apoE4 pathogenicity.
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spelling pubmed-62930202018-12-21 Apolipoprotein E particle size is increased in Alzheimer's disease Nelson, Thomas J. Sen, Abhik Alzheimers Dement (Amst) Genetics INTRODUCTION: Apolipoprotein E4 (apoE4) is the predominant risk factor for late-onset Alzheimer's disease (AD), but the question of which structural differences might explain its effect remains unclear. METHODS: We compared high-density lipoprotein–like apoE particles from 12 AD and 10 control patients using size-exclusion chromatography. RESULTS: ApoE particles from patients genotyped as ε4/ε4 were 2.2 ± 0.3 times as massive as particles from ε3/ε3 control subjects and 1.4 ± 0.1 times as massive as particles from ε3/ε3 AD patients. The increased particle size was not because of incorporation of amyloid β or apoE proteolysis products. Particles from AD patients genotyped as ε3/ε3 were 1.59 ± 0.27 times as massive as ε3/ε3 control subjects. DISCUSSION: Increased particle size in AD is affected by APOE genotype and by disease-related differences in assembly or stability. These differences suggest that lipoprotein assembly or stability in AD brain plays an important role in determining apoE4 pathogenicity. Elsevier 2018-11-13 /pmc/articles/PMC6293020/ /pubmed/30581971 http://dx.doi.org/10.1016/j.dadm.2018.10.005 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Genetics
Nelson, Thomas J.
Sen, Abhik
Apolipoprotein E particle size is increased in Alzheimer's disease
title Apolipoprotein E particle size is increased in Alzheimer's disease
title_full Apolipoprotein E particle size is increased in Alzheimer's disease
title_fullStr Apolipoprotein E particle size is increased in Alzheimer's disease
title_full_unstemmed Apolipoprotein E particle size is increased in Alzheimer's disease
title_short Apolipoprotein E particle size is increased in Alzheimer's disease
title_sort apolipoprotein e particle size is increased in alzheimer's disease
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6293020/
https://www.ncbi.nlm.nih.gov/pubmed/30581971
http://dx.doi.org/10.1016/j.dadm.2018.10.005
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