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Aβ reduction in BACE1 heterozygous null 5XFAD mice is associated with transgenic APP level

BACKGROUND: The β-secretase, BACE1, cleaves APP to initiate generation of the β-amyloid peptide, Aβ, that comprises amyloid plaques in Alzheimer’s disease (AD). Reducing BACE1 activity is an attractive therapeutic approach to AD, but complete inhibition of BACE1 could have mechanism-based side-effec...

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Autores principales: Sadleir, Katherine R, Eimer, William A, Cole, Sarah L, Vassar, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297413/
https://www.ncbi.nlm.nih.gov/pubmed/25567526
http://dx.doi.org/10.1186/1750-1326-10-1
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author Sadleir, Katherine R
Eimer, William A
Cole, Sarah L
Vassar, Robert
author_facet Sadleir, Katherine R
Eimer, William A
Cole, Sarah L
Vassar, Robert
author_sort Sadleir, Katherine R
collection PubMed
description BACKGROUND: The β-secretase, BACE1, cleaves APP to initiate generation of the β-amyloid peptide, Aβ, that comprises amyloid plaques in Alzheimer’s disease (AD). Reducing BACE1 activity is an attractive therapeutic approach to AD, but complete inhibition of BACE1 could have mechanism-based side-effects as BACE1(−/−) mice show deficits in axon guidance, myelination, memory, and other neurological processes. Since BACE1(+/−) mice appear normal there is interest in determining whether 50% reduction in BACE1 is potentially effective in preventing or treating AD. APP transgenic mice heterozygous for BACE1 have decreased Aβ but the extent of reduction varies greatly from study to study. Here we assess the effects of 50% BACE1 reduction on the widely used 5XFAD mouse model of AD. RESULTS: 50% BACE1 reduction reduces Aβ42, plaques, and BACE1-cleaved APP fragments in female, but not in male, 5XFAD/BACE1(+/−) mice. 5XFAD/BACE1(+/+) females have higher levels of Aβ42 and steady-state transgenic APP than males, likely caused by an estrogen response element in the transgene Thy-1 promoter. We hypothesize that higher transgenic APP level in female 5XFAD mice causes BACE1 to no longer be in excess over APP so that 50% BACE1 reduction has a significant Aβ42 lowering effect. In contrast, the lower APP level in 5XFAD males allows BACE1 to be in excess over APP even at 50% BACE1 reduction, preventing lowering of Aβ42 in 5XFAD/BACE1(+/−) males. We also developed and validated a dot blot assay with an Aβ42-selective antibody as an accurate and cost-effective alternative to ELISA for measuring cerebral Aβ42 levels. CONCLUSIONS: 50% BACE1 reduction lowers Aβ42 in female 5XFAD mice only, potentially because BACE1 is not in excess over APP in 5XFAD females with higher transgene expression, while BACE1 is in excess over APP in 5XFAD males with lower transgene expression. Our results suggest that greater than 50% BACE1 inhibition might be necessary to significantly lower Aβ, given that BACE1 is likely to be in excess over APP in the human brain. Additionally, in experiments using the 5XFAD mouse model, or other Thy-1 promoter transgenic mice, equal numbers of male and female mice should be used, in order to avoid artifactual gender-related differences.
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spelling pubmed-42974132015-01-18 Aβ reduction in BACE1 heterozygous null 5XFAD mice is associated with transgenic APP level Sadleir, Katherine R Eimer, William A Cole, Sarah L Vassar, Robert Mol Neurodegener Research Article BACKGROUND: The β-secretase, BACE1, cleaves APP to initiate generation of the β-amyloid peptide, Aβ, that comprises amyloid plaques in Alzheimer’s disease (AD). Reducing BACE1 activity is an attractive therapeutic approach to AD, but complete inhibition of BACE1 could have mechanism-based side-effects as BACE1(−/−) mice show deficits in axon guidance, myelination, memory, and other neurological processes. Since BACE1(+/−) mice appear normal there is interest in determining whether 50% reduction in BACE1 is potentially effective in preventing or treating AD. APP transgenic mice heterozygous for BACE1 have decreased Aβ but the extent of reduction varies greatly from study to study. Here we assess the effects of 50% BACE1 reduction on the widely used 5XFAD mouse model of AD. RESULTS: 50% BACE1 reduction reduces Aβ42, plaques, and BACE1-cleaved APP fragments in female, but not in male, 5XFAD/BACE1(+/−) mice. 5XFAD/BACE1(+/+) females have higher levels of Aβ42 and steady-state transgenic APP than males, likely caused by an estrogen response element in the transgene Thy-1 promoter. We hypothesize that higher transgenic APP level in female 5XFAD mice causes BACE1 to no longer be in excess over APP so that 50% BACE1 reduction has a significant Aβ42 lowering effect. In contrast, the lower APP level in 5XFAD males allows BACE1 to be in excess over APP even at 50% BACE1 reduction, preventing lowering of Aβ42 in 5XFAD/BACE1(+/−) males. We also developed and validated a dot blot assay with an Aβ42-selective antibody as an accurate and cost-effective alternative to ELISA for measuring cerebral Aβ42 levels. CONCLUSIONS: 50% BACE1 reduction lowers Aβ42 in female 5XFAD mice only, potentially because BACE1 is not in excess over APP in 5XFAD females with higher transgene expression, while BACE1 is in excess over APP in 5XFAD males with lower transgene expression. Our results suggest that greater than 50% BACE1 inhibition might be necessary to significantly lower Aβ, given that BACE1 is likely to be in excess over APP in the human brain. Additionally, in experiments using the 5XFAD mouse model, or other Thy-1 promoter transgenic mice, equal numbers of male and female mice should be used, in order to avoid artifactual gender-related differences. BioMed Central 2015-01-07 /pmc/articles/PMC4297413/ /pubmed/25567526 http://dx.doi.org/10.1186/1750-1326-10-1 Text en © Sadleir et al.; licensee BioMed Central. 2015 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Sadleir, Katherine R
Eimer, William A
Cole, Sarah L
Vassar, Robert
Aβ reduction in BACE1 heterozygous null 5XFAD mice is associated with transgenic APP level
title Aβ reduction in BACE1 heterozygous null 5XFAD mice is associated with transgenic APP level
title_full Aβ reduction in BACE1 heterozygous null 5XFAD mice is associated with transgenic APP level
title_fullStr Aβ reduction in BACE1 heterozygous null 5XFAD mice is associated with transgenic APP level
title_full_unstemmed Aβ reduction in BACE1 heterozygous null 5XFAD mice is associated with transgenic APP level
title_short Aβ reduction in BACE1 heterozygous null 5XFAD mice is associated with transgenic APP level
title_sort aβ reduction in bace1 heterozygous null 5xfad mice is associated with transgenic app level
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297413/
https://www.ncbi.nlm.nih.gov/pubmed/25567526
http://dx.doi.org/10.1186/1750-1326-10-1
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